161335183-900-inorganic-questions-for-IIT-JEE-ADVANCED[1].pdf

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IIT-JEE

INORGANIC PAPER Q.1

CHEMISTRY

P. JOY

Reactions of aluminium with 1. O2

2. N2

3. Cl2

4. Cr2O3

5. Mn3O4

6. HCl

7. H2SO4(Dil.)

8. H2SO4 (Conc.)

9. HNO3

10. NaOH

11. AlCl3 Q.2

Reactions of Al(OH)3 with 1. Acid 2. NaOH 3. Heating Below 450ºC 4. Heating above 450ºC

Q.3

What is the general formula of alum.

Q.4

How many water molecules act as ligands about mono and trivalent metal cations.

Q.5

Which unipositive cations do form alum.

Q.6

Which tripositive cations do form alum.

Q.7

How do structures of all alums differ.

Q.8

Which alkali metal cation does not form alum.

Q.9

What happens when alums are heated.

Q.10

What are the major uses of alum.

Q.11

What is the nature of aqueous solution of alums.

Q.12

How are alums prepared.

Q.13

What are pseudo alums.

Q.14

Are pseudo alums isomorphous to alums.

Q.15

What is feather alum or hair salt.

Q.16

How can you prove that Al(OH)3 is amphoteric in nature.

Q.17

How Al(OH)3 ppt is different than Zn(OH)2 ppt

Q.18

How Al2Cl6 is prepared.

Q.19

How Al2O3 can be converted into Al2Cl6

Q.20

In which conditions does Al2Cl6 exist.

Q.21

What happens when Al2Cl6 dimer is added to water.

Q.22

Are the bonding states of Al2Cl6 in vapour phase and in aqueous phase are different.

Q.23

What is the nature of AlCl3 in aqueous state.

Q.24

Does AlCl3 on heating melts.

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INORGANIC PAPER

IIT-JEE

P. JOY

CHEMISTRY

Q.25

Why is it difficult keep AlCl3 dry

Q.26

Comment on stability of AlCl

Q.27

What happens when AlCl3 reacted with Cl–

Q.28

What happens when Al2Cl6 is reacted with LiH

Q.29

Which is the most stable compound of aluminium.

Q.30

What are the different forms of alumina.

Q.31

What is corundum.

Q.32

What is thermite reaction.

Q.33

What happens when AlCl3 vapours are passed over fused Al2O3 at 1000ºC.

Q.34

Which form of alumina is corundum.

Q.35

Which form of alumina is acid soluble.

Q.36

Why 'C' shows highest properties of catenation ?

Q.37

Which element of fourth group donot show allotropy ?

Q.38

Which allotrope of carbon is thermodynamically more stable ?

Q.39

Which of two has a dipole moment CO & CO2 ?

Q.40

Which element of group IV does not show allotropy ?

Q.41

Why graphite is good conductor of electricity ?

Q.42

Which is thermodynamically most stable ? Graphite, Diamond or fullerene ?

Q.43

Which element occurs in both very hard and very soft form ?

Q.44

In which form does silicon show its allotropy ?

Q.45

What are three crystalline modifications of tin ?

Q.46

How various allotropes of tin are related to temperature ?

Q.47

What is tin disease, tin pest or tin plague ?

Q.48

What is tin cry ?

Q.49

Which element of IV group has maximum number of Isotopes ?

Q.50

Which allotrope of carbon is insoluble solvent ?

Q.51

What are the oxides of carbon ?

Q.52

Which acid anhydride is CO2 ?

Q.53

Which acid anhydride is CO ?

Q.54

How fullerence was originally prepared ?

Q.55

Can fullerence be prepared by evaporation of graphite by electric arc ?

Q.56

How many 'C' atoms are there normally in fullerence ?

Q.57

What is the colour of C60 in toluene ?

Q.58

What is the colour of C70 in Toluene ?

-ions

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IIT-JEE

INORGANIC PAPER

CHEMISTRY

P. JOY

Q.59

What is the shape of C60 ?

Q.60

Which acid anhydride is carbon sesquioxide C3O2 ?

Q.61

Which oxide of IV group is not solid ?

Q.62

Which monoxide of IV group does not exist ?

Q.63

Which monoxide of IV group is neutral ?

Q.64

What is the nature of IV group monoxides ?

Q.65

Which IV group oxides are network solids ?

Q.66

Why bicarbonates are alkaline in nature although they has H+ ?

Q.67

How calcium cyanamide can be prepared from CaC2 ?

Q.68

What happens when calcium cyanamide is hydrolysed ?

Q.69

What happens when calcium cyanamide is heated with Coke & NaCl

Q.70

What happens when K4Fe(CN)6 is heated strongly ?

Q.71

What happens when KCN & dil. H2SO4 reacts ?

Q.72

What is the nature of aqueous solution of KCN ?

Q.73

What happens when HCN is oxidised by O2, Ag, Cu2+ ?

Q.74

Why (CN)2 is pseudohalide ?

Q.75

Why CO2 is molecule but SiO2 is 3D network solid ?

Q.76

What are the nature of CO2, SiO2, GeO2, SnO2, PbO2 ?

Q.77

What happens when Pb(NO3)2 is strongly heated ?

Q.78

Which dioxide of nonmetal C, S, N or Cl does not act as reducing agent ?

Q.79

What happens when graphite is heated with KMnO4 ?

Q.80

What is the general formula of organosilicone ?

Q.81

What happens when dialkyldichloro silanes of diaryl dichlorosilanes are subjected to hydrolysis ?

Q.82

What is the hybridisation state of Si in SiO2 ?

Q.83

What is the purest form of silicon ?

Q.84

What happens when SiO2 is reacted (heated) with alkalis and alkali metal carbonates ?

Q.85

What happens when SiO2 is reacted with following ? (a) KOH

(b) CaCO3

(c) KNO3

Q.86

What type of glass is K2O.PbO.4SiO2 ?

Q.87

What is the definition of glass ?

Q.88

Why HF acid is stored in plastic bottles and not glass bottles ?

Q.89

Which compound is formed when glass reacts with HF ?

Q.90

What is the formula of soda glass ?

Q.91

What is the formula of water glass

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(d) HF

(e) Coke

PAGE # 3

INORGANIC PAPER

IIT-JEE

CHEMISTRY

P. JOY

Q.92

What is silica Garden ?

Q.93

What are silanes and germanes ? What are their general formula.

Q.94

What happens when mixture of silane and H2 is bubbled through water ?

Q.95

What happens when Si is fused with NaOH in air ?

Q.96

Which acid is used for etching glass ?

Q.97

How silanes are different than alkanes ?

Q.98

KNO3 on heating produce KNO2 and O2 but what happens when KNO3 is heated with SiO2 ?

Q.99

Name an acid which dissolves silica ?

Q.100

What are corundum and carborundum ?

Q.101

What pseudo solids ?

Q.102

Which allotrope of Si is isomorphous with carbon ?

Q.103

What is Na2SiO3. CaSiO3.4SiO2 ?

Q.104

What do you call K2O.CaO.4SiO2 ?

Q.105

Which type of anions are present in pyrex glass ?

Q.106

Which type of glass are prisms and lenses are made up of ?

Q.107

What is Crookes glass ? What is its speciality ? Which metal compound is present in it ?

Q.108

Which type of glass has lane thermal expansion ?

Q.109

How borosilicate glass are obtained ?

Q.110

Why trimethyl amine is pyramidal but trisilyl amine is planar ?

Q.111

Which of two is more basic N(CH3)3 or N(SiH3)3 ?

Q.112

How the name silicone is derived for the polymer R2SiO ?

Q.113

Why CO2 is a gas while SiO2 is a solid ?

Q.114

Why CCl4 does not hydrolyse but SiCl4 ?

Q.115

How tin is purified ?

Q.116

Which oxide of tin (SnO, SnO2) is/are amphoteric ?

Q.117

Why heating of SnC2O4 does not yield SnO instead of SnO2 ?

Q.118

What happens when SnO2 is reacted with (i) H2SO4 (ii) NaOH

Q.119

What happens when SnCl2.2H2O crystals are heated ?

Q.120

Which of the two SnCl2 or SnCl4 is a liq. at room temperature ?

Q.121

What is butter of Sn ? What is its major use.

Q.122

What are the addition compounds of SnCl2 & NH3 ?

Q.123

What is the double salt of SnCl4 with NH3 ?

Q.124

How calamel is produced by SnCl2 ?

Q.125

Which tin compound is used in tooth paste to help tooth decay ?

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INORGANIC PAPER

IIT-JEE

CHEMISTRY

P. JOY

Q.126

Which property of tin makes it useful for tinning of utensils ?

Q.127

What happens when AuCl3 is treated with SnCl2 ?

Q.128

How PURPLE OF CASIUS is formed ?

Q.129

What happens when butter of tin is hydrolysed with excess of water ?

Q.130

What happens when tin metal is reacted with conc. HNO3 ?

Q.131

Which tin halide out of SnCl4, SnBr4, SnI4 is coloured ?

Q.132

How Tin (II) fluoride is obtained ?

Q.133

Why Pb715 has higher I.E. than Sn707 ?

Q.134

What are various oxides of Pb ?

Q.135

Why do PbCl4 acts as strong oxidising agent ?

Q.136

SiF62– exist but not CF62– explain why ?

Q.137

What is the order of ease of catenation ?

Q.138

How many allotropes of Sn exist ?

Q.139

Why PbCl2 is ionic where is PbCl4 is covalent.

Q.140

How do following properties vary ? (a) Atomic radii (b) Melting point and boiling point (c) Density (d) I.E. (e) O.S.

Q.141

Why Group V elements have much higher I.E. than group IV elements.

Q.142

Which two elements of Group V are metalloids ?

Q.143

Why Bi has low melting point ?

Q.144

What are the important oxidation states exhibited by Group V elements ?

Q.145

Give an example of each of compound in which 'N' is having oxidation states –3 to +5

Q.146

Why Group V elements have poor catenation property ?

Q.147

What is the structure of hydrazoic acid ?

Q.148

Which elements of Group V do not show allotropy ?

Q.149

What are the allotropes of phosphorous ?

Q.150

What are the allotropes of Arsenic ?

Q.151

What are the allotropes of Antimony ?

Q.152

Which element of group V has tendency to form pπ – pπ bond ?

Q.153

Why N2 is less reactive than other members of its family ?

Q.154

What is the formula of elemental state of group V elements.

Q.155

What type of π bond is present in POX3. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER

IIT-JEE

CHEMISTRY

P. JOY

Q.156

What happens when Ca3N2 and Ca3P2 are added to water ?

Q.157

What happens when Zn3As2, Zn3Sb2, Zn3Bi2 are added to water ?

Q.158

Which compound is formed when NH3 gas is passed into NaOCl solution.

Q.159

Arrange following hydrides in increasing bond angle NH3, PH3, AsH3, SbH3

Q.160

Arrange following hydrides in the increasing order of their thermal stability NH3, PH3, AsH3, SbH3, BiH3

Q.161

Which hydride of group V is strongest reducing agent ?

Q.162

Which V group hydride is the weakest reducing agent.

Q.163

On moving down the group generally b.p. of group V hydrides increases except NH3. Why NH3 has higher b.p. than PH3 and AsH3 ?

Q.164

What is order of Lewis base character of V group metal hydrides.

Q.165

Which trihalide of group V elements is not covalent but ionic ?

Q.166

What is the shape of group V trihalides ?

Q.167

Write hydrolysis product of following trihalides PCl3, AsCl3, SbCl3, BiCl3

Q.168

Why nitrogen trihalides cannot be hydrolysed ?

Q.169

Do fifth group trihalides work as Lewis acid ?

Q.170

Which fifth group element does not form pentahalide ?

Q.171

Which of the two trihalide or pentahalide of fifth group is thermally more stable ?

Q.172

Do all pentahalides act as Lewis acids ?

Q.173

What are the formula of PCl5 in gaseous state and in solid state ?

Q.174

Draw the structure of PCl5 in solid state.

Q.175

How white phosphorous is obtained from calcium phosphate ?

Q.176

Which form of phosphorous has garlic smell ?

Q.177

Which form of phosphorous is toxic.

Q.178

Which form of phosphorous is soluble in CS2 but insoluble in water ?

Q.179

What is the structure of phosphorous in solid and vapour state ?

Q.180

Which form of phosphorous spontaneously burn in air with green flame ?

Q.181

What happens when (a) White phosphorous is heated upto 540 K in inert atmosphere. (b) White phosphorous is heated upto 450 K at 1200 atm pressure.

Q.182

What is the structure of Red phosphorous.

Q.183

Which form of phosphorous is insoluble in both water and CS2 ?

Q.184

What happenes when phosphorous combine with metals like Ca and Mg, Na and K.

Q.185

Why white phosphorous is kept in water ?

Q.186

Which is formed by the combustion of phosphorous in air ?

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INORGANIC PAPER

IIT-JEE

CHEMISTRY

P. JOY

Q.187

Which two products are formed by heating phosphorous with NaOH ?

Q.188

What white phosphorous is ? A good reducing agent or a good oxidising agent ?

Q.189

What are products when HNO3, conc. H2SO4, CuSO4, AgNO3 are reduced by white phosphorous ?

Q.190

What happens when white phosphorous is reacted with following nonmetals (a) Cl2, (b) S8.

Q.191

Which form of phosphorous red or white reacts with NaOH to produce pH3 ?

Q.192

What happenes when following are reacted with water (a) Ca3P2, (b) Na3P.

Q.193

How AlP can be decomposed into pH3 ?

Q.194

What happenes when phosphorous acid is strongly heated ?

Q.195

How phosphene is prepared in laboratory ?

Q.196

What are vortex rings formed by PH3 ? Why these rings are formed ?

Q.197

How vortex rings of PH3 can be prepared in laboratory.

Q.198

Why NF3 is not hydrolysed ?

Q.199

Why PF3 and PF5 are not hydrolysed ?

Q.200

Write the hydrolysis product of following compounds NCl3, PCl3, AsCl3, SbCl3, BiCl3.

Q.201

Why penlahalide like BiF5 does not exist ?

Q.202

B, Ga, Al, Tl, In [First Ionisation Energy]

Q.203

BF3, BBr3, BCl3, BI3 [Lewis Acid Strength]

Q.204

BCl3, GaCl3, AlCl3, InCl3 [Lewis Acid Strength]

Q.205

B2O3, Al2O3, In2O3, Tl2O3, Ga2O3 [Basic Stregnth]

Q.206

B, Ga, Al, In, Tl [Stability of +3 oxidation state]

Q.207

Ga, Tl, In [Stability of +1 oxidation state]

Q.208

B, Ga, Al, In, Tl [Stability of hydride]

Q.209

Al, In, Ga, Tl [Reducing nature]

Q.210

C, Si, Sn, Ge, Pb [First Ionisation Energy]

Q.211

C, Si, Sn, Ge, Pb [Catenation]

Q.212

C, Si, Sn, Ge, Pb [Ionisation Energy]

Q.213

PbF2, PbCl2, PbBr2, PbI2 [Ionic Character]

Q.214

C, Si, Sn, Ge, Pb [Density]

Q.215

N, As, P, Sb, Bi [Melting Point]

Q.216

N, As, P, Sb, Bi [Boiling Point]

Q.217

NH3, AsH3, BiH3, PH3, SbH3 [Basic Strength]

Q.218

NH3, AsH3, BiH3, PH3, SbH3 [Reducing Character]

Q.219

NH3, PH3, AsH3, SbH3 [Boiling point]

Q.220

NI3, NCl3, NBr3, NF3 [Basic Character]

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CHEMISTRY

Q.221

NH3, AsH3, PH3, BiH3, SbH3 [Bond Angle]

Q.222

PCl3, SbCl3, AsCl3 [Acid Strength]

Q.223

N2O3, As2O3, P2O3 [Acidic Strength]

Q.224

N2O5, As2O5, P2O5, Bi2O5, Sb2O 5 [Acidic Strength]

Q.225

N2O, N2O 3, NO, N2O4, N2O5 [Acidic Strength]

Q.226

P2O5, Sb2O5, As2O5, Bi2O5, N2O5 [Stability]

Q.227

NCl3, AsCl3, PCl3, SbCl3, BiCl3 [Ease of hydrolysis]

Q.228

PF3, PBr3, PCl3, PI3 [Acid Strength]

Q.229

PF3, PCl3, PBr3, PI3 [Bond Angle]

Q.230

HNO3, H3AsO4, H3PO4, H3SbO4 [Strength and solubility]

Q.231

O, Se, S, Te [Electron Affinity]

Q.232

O, Se, S, Te, Po [Ionisation potential]

Q.233

H2O, H2S, H2Te, H2Se [Reducing power]

Q.234

H2O, H2S, H2Te, H2Se [Bond angles]

Q.235

H2O, H2S, H2Te, H2Se [Stability]

Q.236

H2O, H2S, H2Te, H2Se [Acidic nature]

Q.237

H2O, H2S, H2Te, H2Se [Dipole moment]

Q.238

SO3, TeO3, SeO3 [Acidic nature]

Q.239

SO, SO2, SO3 [Acidic nature]

Q.240

H2SO3, H2SeO3, H2TeO3 [Acidic strength]

Q.241

F, Cl, Br, I [Electron affinity]

Q.242

F, Cl, Br, I [Electronegativity]

Q.243

Cl2, Br2, F2, I2 [Bond energy]

Q.244

Cl2, Br2, F2, I2 [oxidising power]

Q.245

HF, HCl, HBr, HI [Acidic strength]

Q.246

HF, HCl, HBr, HI [Reducing character]

Q.247

HF, HCl, HBr, HI [Boiling point]

Q.248

HF, HCl, HBr, HI [Thermal stability]

Q.249

HClO, HClO2, HClO3, HClO4 [Thermal stability]

Q.250

HClO, HBrO, HIO [Thermal stability]

Q.251

HClO3, HBrO3, HIO3 [Thermal stability]

Q.252

HClO, HClO2, HClO3, HClO4 [Acidic strength]

Q.253

HClO, HBrO, HIO [Acidic strength]

Q.254

HClO, HClO2, HClO3, HClO4 [Oxidising power]

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INORGANIC PAPER

IIT-JEE

CHEMISTRY

P. JOY

Q.255

MF, MCl, MBr, MI [Ionic character]

Q.256

I3+, I3–, H5IO6, I2O5, I– [Oxidation number]

Q.257

HClO3, HClO4, HClO2, HClO [Acidic strength]

Q.258

I2, HI, HIO4, ICl [Oxidation number]

Q.259

He, Ar, Ne, Kr, Xe [Polarizability]

Q.260

He, Ar, Ne, Kr, Xe [Solubility in water]

Q.261

XeF2, XeF4, XeF6 [Melting point]

Q.262

What is liquor ammonia ?

Q.263

Why decomposition temperature of NH3 will be highest ?

Q.264

What is the colour of the flame produced when NH3 burns in pure oxygen.

Q.265

Ammonia will burn in air ? Yes or No.

Q.266

Which factor is responsible for high boiling point of NH3.

Q.267

Name the process by which ammonia is made industrially.

Q.268

How liquid NH3 resembles water in its physical behaviour.

Q.269

Which factor is responsible for making liquid NH3 a fair ionizing solvent. Why NH3(l) is a better solvent for organic compounds but generally a poorer one for ionic inor-

Q.270

ganic compounds. Q.271

Why AgI is exceedingly insoluble in water but good soluble in NH3.

Q.272

Name the two species formed when liquid ammonia undergoes autodissociation.

Q.273

Which type of reaction occurs when liquid ammonia undergoes autodissociation.

Q.274

Sodium in liquid ammonia is most widely used as a reducing agent or oxidising agent.

Q.275

What are the gases produced when (NH4)2Cr2O7 is heated.

Q.276

What are the gases produced when NH4NO3(s) is dissociated.

Q.277

What are the gas as produced when NH4NO3(l) is decomposed when heated.

Q.278

What is the structure of N2O.

Q.279

How many unpaired electron(s) are present in NO.

Q.280

Which type of molecular orbital, is occupied by unpaired electron(s). Equimolar mixture of which two oxides of nitrogen on condensing at how temperature gives N2O3,

Q.281

as a blue solid. Q.282

Which gas is produced on thermal decomposition of lead nitrate.

Q.283

Which gas is produced on when copper dissolve in conc. HNO3

Q.284

Solid N2O4 is diamagnetic or paramagnetic.

Q.285

What is the anhydride of nitric acid.

Q.286

In which state (liquid, gas, vapour, solid) covalent N 2O5 molecules are present.

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IIT-JEE

INORGANIC PAPER Q.287

P. JOY

CHEMISTRY

Complete the following reaction 50ºC

→ Fe(CO)5 + NO Pr essure Whether the product formed is ionic or covalent. Q.288

Which compound is formed when NO is reacted with freshly prepared FeSO4 solution.

Q.289

What are the two classess in which phosphorus oxo acids can be divided.

Q.290

What are the formal oxidation states of two oxoacids of phosphorus.

Q.291

How many nonacidic hydrogen atoms are attached directly to phosphorus acids.

Q.292

Consider the following reaction

O

A g+

Ag

P H

OH

C r2 O 7

2–

H

C r +3

H ypophosphorous acid

In the above reaction hypophosphorous acid act as an oxidising agent or reducing agent. Q.293

Which allotropic form of phosphorous is used in preparing hypophosphorus acid from Ba(OH)2.

Q.294

How many acidic hydrogen(s) is/are present in H3PO2.

Q.295

Which phosphorus acid is formed on reaction between water and phosphorous trichloride at 0ºC.

Q.296

Is it possible to obtain polymeric phosphates with layer structures similar to those found in some of the polysilicates.

Q.297

Which phosphoric acid is prepared by treating phosphate rock with sulfuric acid.

Q.298

Which phosphoric acid on dehydration produces orthophosphoric acid.

Q.299

Which oxoacids of phosphorus are tetrabasic acid ?

Q.300

What is the general formula by which cyclic polymetaphosphates can be represented.

Q.301

What are the two main oxoacids of nitrogen.

Q.302

What are the properties possessed by HNO2.

Q.303

Which oxoacid of nitrogen act as both reducing and oxidising agent.

Q.304

What is fuming nitric acid.

Q.305

In which type of solution HNO2 is stable.

Q.306

What is Aqua fortis and what is its meaning.

Q.307

Name the two processess by which HNO3 can be prepared.

Q.308

Aqueous nitric acid is an oxidant, which ion is responsible for this property.

Q.309

What are the products formed when NH2CONH2 is treated with HNO2. Write the balanced equation.

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INORGANIC PAPER

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P. JOY

Q.310

Which two oxyacids of nitrogen are explosive in nature.

Q.311

How nitric acid is manufactured industrially.

Q.312

Which oxide is used to convert nitric acid to its anhydride.

Q.313

What are the oxides produced when N2O4 is dissolved in water.

Q.314

When HNO3 is dissolved in pure H2SO4, an active agent is formed which has an important application in organic chemistry. Name the agent.

Q.315

What are the two oxides of phosphorus.

Q.316

Which compound is formed when P2O3 combines with oxygen.

Q.317

What happens when P2O3 (i) Combines with cold water

(ii) Combines with hot water.

Write the corresponding reactions. Q.318

Which oxide of phosphorus acts as Dehydrating agent.

Q.319

Which oxide of phosphorus is highly, poisonous in nature.

Q.320

Which oxide of phosphorus converts HNO3 to N2O5 and H2SO4 to SO3.

Q.321

What happens when P2O5 (i) Combines with cold water.

(ii) Combines with hot water.

Write the corresponding reactions. Q.322

If ammonia in large excess is treated with Cl2 diluted with N2, what product is produced. Write the balanced equation.

Q.323

Which compound is formed when chloramine reacts with NH3.

Q.324

Consider the sequence for industrial utilization of atmospheric nitrogen. H

O2 +H2O O2 2 → NH3   → HNO3(aq) → NO   N2  

Haber process

(I)

(II)

(III)

(IV)

Name the process by which II is converted into III. Q.325

Complete the following reaction 4NH3(g) + 3O2(g) l

Q.326

At 750–900ºC and in the presence of a platinum catalyst ammonia reacts with oxygen to give other product instead of O2. What is the product formed.

Q.327

How many allotropes of oxygen are present.

Q.328

Give the two laboratory methods for the preparation of oxygen.

Q.329

What are the gases produced on reaction of oxygen with carbon disulphide.

Q.330

Which oxide is present is the compound when Na(s) reacts O2(g).

Q.331

What is the colour of liquid dioxygen and solid dioxygen. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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P. JOY

Q.332

Name the compound in which the oxygen shows an oxidation state of + 2.

Q.333

Can oxygen show oxidation state beyond 2.

Q.334

Why OF6 is not known.

Q.335

How oxygen can be obtained from bleaching powder.

Q.336

What is an acidic oxide ? Give an example.

Q.337

What is an basic oxide ? Give an example.

Q.338

What is an amphoteric oxide ? Give an example.

Q.339

Which elements generally form amphoteric oxides.

Q.340

Which acid is produced on reaction of SO2 with water.

Q.341

Which type of solution (alkaline, acidic or neutral) is produced on reaction of BaO with water.

Q.342

Which gas is produced when ZnO reacts with an acid.

Q.343

Which factor is responsible for stability of an ionic metal oxide.

Q.344

Give an example of ionic oxides with some covalent character.

Q.345

What are the product(s) formed when H2S react with O2.

Q.346

How many lone pairs of electron are present in OF2 molecule.

Q.347

Arrange the following species in decreasing order of their bond strength. O2, O2+, O2–, O22–

Q.348

Which gas is produced when sodium nitrate decomposes above 800ºC.

Q.349

Is oxygen has highest electron affinity in group 16 ?

Q.350

What is the oxidation state of O in Na2O2 ?

Q.351

Arrange the following oxides in increasing order of their acidic property. ZnO, Na2O2, P2O5, MgO.

Q.352

What are the factors which are responsible for anomalous behaviour of oxygen.

Q.353

Who discovered oxygen.

Q.354

Which factor is responsible for existence of oxygen as discrete diatomic molecule.

Q.355

Is ozone linear or non linear molecule.

Q.356

How does oxygen and ozone differ in their magnetic nature ?

Q.357

Which ion is isoelectronic with ozone.

Q.358

How does oxygen is converted into ozone.

Q.359

What is the bond angle < O – O – O in ozone.

Q.360

What change occurs in volume of ozone when it is heated.

Q.361

Which is more powerful oxidizing agent O3 or O2.

Q.362

Give two applications of ozone. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER

CHEMISTRY

Q.363

To which group of the periodic table, ozone belong ?

Q.364

Can ozone oxidises

P. JOY

(i) Lead sulphide. (ii) Potassium iodide (iii) Mercury Q.365

What is the oxidation state of oxygen in O3.

Q.366

What is the percentage of ozone in ozonised oxygen ?

Q.367

What is the change in the oxidation state of P occurs when ozone reacts with phosphorus. Give an chemical equation.

Q.368

There are two different values of O–O bond length in ozone ? True or False.

Q.369

Which halogen (Chlorine or Fluorine) interacts with water to form ozone.

Q.370

Ozone has a dark blue colour. Absorption of which colour of light is responsible for its blue colour.

Q.371

Which type of radiation from the sun is absorbed by the ozone layer in the upper atmosphere.

Q.372

Which compounds are blamed for making holes in ozone layer.

Q.373

Complete the following reaction : O3 + 2K+ + 2I– + H2O   →

Q.374

In which phase hydrogen bonded molecules of H2O2 are found.

Q.375

Which is more associated via hydrogen bonding i.e. H2O or H2O2.

Q.376

What is the structure of the molecule of H2O2.

Q.377

Which has more density H2O or H2O2

Q.378

What is the limitations of H2O2 which inhibits its utility as an ionizing solvent.

Q.379

Is H2O2 is more acidic than H 2O in dilute aq. solution.

Q.380

H2O 2 acts as oxidizing agent or reducing agent towards MnO4–

Q.381

In which type of solution (acid or basic), oxidations with H2O2 is slow.

Q.382

In which type of solution (acid or basic) disproportionation of H2O2 occurs most rapidly

Q.383

Which free radicals are formed by metal ion catalysed decomposition of H2O2.

Q.384

Identify the products of the following reaction O2 H2SO 4 BaO   → BaO2   → A + B.

Give the structure and name of the reactant involved in the synthesis of H2O 2 by the reaction given below.

Q.385

O Reactant

C 2H 5

O2 H 2 /Pd .

+ H2 O 2

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INORGANIC PAPER Q.386

IIT-JEE

CHEMISTRY

P. JOY

Consider the following reaction H2O2(l) → H2O(l) + ½O2

∆G = – 121.4 kJ mol–1

Is water or oxygen is thermodynamically unstable with respect to H2O 2. Q.387

Which acid on hydrolysis give H2O2. Write a chemical equation.

Q.388

Arrange the following O2, H2O and O3 in increasing order of their O – O bond length.

Q.389

How many atoms of sulphur are present in its free state.

Q.390

Which ore of sulphur is also called as Fool's gold.

Q.391

Name the process by which sulphur is generally extracted from underground sulphur bearing rocks.

Q.392

Which allotropic form of sulphur is considered as a supercooled liquid.

Q.393

How milk of sulphur is prepared.

Q.394

Below which temperature β-sulphur is converted into α-sulphur and what this temperature is called.

Q.395

Complete the following reactions : Boil (i) 2S + Cl2   → ∆ (ii) 3S + P4    → 1200 −1400K (iii) 2S + C   →

Q.396

What compound is formed when sulphur reacts with NH3 in presence of H2S gas.

Q.397

Which oxide of sulfur is closely related structurally & electronically to ozone.

Q.398

What is the structure and bond angle of SO3.

Q.399

Which oxide of sulphur act as an antichlor for removing excess of chlorine.

Q.400

Which property of SO2 is responsible for its bleaching action.

Q.401

Which oxide of sulphur is used in the preparation of H2SO4.

Q.402

What is oxidation state of sulphur in SO2 & SO3 respectively.

Q.403

Give two methods for preparation of Hydrogen Sulphide.

Q.404

H2S is a dibasic acid or monobasic acid.

Q.405

Name the two series of salts formed by H2S.

Q.406

Which property of H2S is used for detection of various cations in laboratory.

Q.407

What happens when SO2 is passed through acidified solution of H2S.

Q.408

Why coordination compounds of H2S are very rare.

Q.409

H2S in large doses prove fatal. What is antidote of H2S.

Q.410

Which acid is called king of chemicals and why is it so called.

Q.411

Name the two processess by which sulphuric acid can be manufactured.

Q.412

What are the ideal conditions required for manufacturing of H2SO4 by contact process. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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CHEMISTRY

P. JOY

Q.413

What is the strength of H2SO4 produced by chamber process.

Q.414

By which process 100% pure H2SO4 is obtained.

Q.415

Which removes impurities of arsenic in contact process.

Q.416

Why SO3 is never directly dissolved in H2O to form H2SO4.

Q.417

Write down the chemical reactions taking place in contact process.

Q.418

H2SO4 has low volatility. Why ?

Q.419

Name the two series of salts formed by H2SO4.

Q.420

How many oxygen atoms in H2SO4 are linked to sulphur by single covalent bonds.

Q.421

What is the oxidation state of sulphur in H2SO4.

Q.422

Which type of bond is responsible for associated structure of H2SO4.

Q.423

It is suggested that to dilute conc. H2SO4, always add conc. H2SO4 to water and never water to conc. H2SO4. Why ?

Q.424

Why conc. H2SO4 is used extensively to prepare other acids.

Q.425

Why H2SO4 has great affinity for water.

Q.426

What are the functions of H2SO4 in the reaction given below. 2Ag + H2SO4 → Ag2SO4 + 2H2O + SO2

Q.427

Why sugar becomes black when it comes in contact with conc. H2SO4.

Q.428

Which acid is consumed when a lead storage battery is discharged.

Q.429

Which acid can be used as an oxidising agent, reducing agent and bleaching agent.

Q.430

What are the oxidation number of both the S in Na2S2O3.

Q.431

Why hypo is used in iodometric titrations.

Q.432

Why hypo is used as a fixing agent in photography.

Q.433

What are the products formed when chlorine is passed through aqueous hypo solution.

Q.434

When hypo is heated to high temperatures, the products are.

Q.435

Sulphur disappears when it is boiled in a solution of sodium sulphite. This is due to formation of.

Q.436

Write the spring's reaction for formation of Na2S2O3.

Q.437

Which ion is produced when thiosulphate is oxidised by iodine.

Q.438

What are hydrohalic acids ?

Q.439

Why halogen react very easily and yield hydrogen halide.

Q.440

Complete the reactions : ∆ (i) CaF2 + H2SO4   → ∆ (ii) 2NaCl + H2SO4   →

Q.441

Which hydrogen halide is liquid at room temperature.

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INORGANIC PAPER

CHEMISTRY

P. JOY

Q.442

What is the increasing order of acidic strength of hydrohalic acids.

Q.443

Give two reasons for weak acidic character of HF.

Q.444

Why fluorine forms salts of the type KHF2.

Q.445

Why acidity of anhydrous HF is considerably increased in the presence of super acid, SbF5. Write a chemical reaction involved.

Q.446

Which hydrohalic acids has the highest value of dipole moment.

Q.447

Which hydrohalic acid does not form precipitate with AgNO3.

Q.448

Write the increasing order of reducing power of halogen acids.

Q.449

Dilute solution of HF cannot be concentrated beyond 36% by distilling only. Why ?

Q.450

Why HF is not stored in glass bottles.

Q.451

Which acid is used for etching the glass.

Q.452

Which is the most volatile among the following compounds HI, HCl, HF, HBr

Q.453

Which hydrogen halide has the highest molar heat of vaporization.

Q.454

Consider the following reaction HNO3 + HF → H2NO3+ + F– Which species act as base.

Q.455

Arrange the following compounds in increasing order of their bond strength HF, HCl, HBr, HI

Q.456

KF combines with HF to form KHF2. What are the species present in the KHF2.

Q.457

Which halogen forms least number of oxyacid.

Q.458

Arrange the following acids in decreasing acid strength. ClOH, BrOH, IOH

Q.459

Arrange the following in increasing order of acidity, HClO, HClO2, HClO3, HClO4

Q.460

What is the oxidation state of chlorine in hypochlorous acid.

Q.461

Consider the following reaction HClO2  → HOCl  → ½Cl2 I

II

III

Conversion of II into III will increases or decreases the oxidation number of chlorine. Q.462

Give a method for preparing HClO2.

Q.463

What are the salts of HClO2 called ?

Q.464

Which oxyacids of chlorine is the least oxidizing in nature. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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CHEMISTRY

Q.465

Salts (0.1 M solution) of which oxyacid of chlorine is most basic ?

Q.466

Consider the following reaction

P. JOY

NH3 + NaOCl  → X + NaOH – Gum X + NH3 + OH–   → H2N – NH2 + Cl + H2O

Identify the X & what is it called. Q.467

What is the shape of ClO2– & what is the hybridisation state of Cl.

Q.468

Draw the structure of ClO2–.

Q.469

Which oxyacid of chlorine has highest oxidation number.

Q.470

Arrange the oxyacids of chlorine is increasing order of their thermal stability.

Q.471

Arrange the oxyacids of chlorine in increasing order of their thermal stability.

Q.472

Arrange the following compounds in increasing order of their thermal stability HIO3, HClO3, HBrO3

Q.473

BY which mechanism HOCl is formed from Cl2 in water write a chemical reaction.

Q.474

What is the hybridisation state of chlorine in oxyacids of chlorine.

Q.475

What are the natue of oxides of Halogens.

Q.476

Which halogens forms acidic oxides.

Q.477

Which oxide of chlorine is least acidic and which is most acidic.

Q.478

Which oxide of chlorine is paramagnetic is nature.

Q.479

Aqueous solution of bleaching power gives a test of which ions.

Q.480

Name the type of reaction as given below CaOCl2 + H2O  → Ca(OH)2 + Cl2

Q.481

What products are obtained by auto oxidation of bleaching power.

Q.482

Bleaching powder loses its bleaching property when it is kept in open bottle for long time. Why.

Q.483

Write the chemical equation involed in Hasenclever method for preparation of CaOCl2.

Q.484

Which gas is liberated when excess of dil. acids (H2SO4, HCl, HNO3) reacts with CaOCl2.

Q.485

What do you mean by available Cl2.

Q.486

Why CaOCl2 uses as a disinfectant.

Q.487

Why CaOCl2 gives Cl2 like smell.

Q.488

Bleaching power is an example of ..... salt.

Q.489

What % of available Cl2 is present in a good quality of bleaching powder.

Q.490

Is bleaching power is priced according to its crystal size.

Q.491

What is the meaning of halogens ?

Q.492

Which group 17 element is radioactive ? VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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P. JOY

CHEMISTRY

Q.493

What are chalcogens ?

Q.494

Which group elements have greater similarities within group than other group in periodic table.

Q.495

Why halogens do not occur in free elemental state ?

Q.496

What are the generally found form of iodine ?

Q.497

What are the generally found forms of other halogens ?

Q.498

Which halogen is most abundant ?

Q.499

What was moissan method of fluorine formation ?

Q.500

Why diaphragm made of Teflon is used to separate anode from cathode in preparation of fluorine.

Q.501

How bromine is commercially obtained ?

Q.502

How iodides are converted into iodine.

Q.503

How iodates can be converted into I2 ?

Q.504

What is correct when conc. H2SO4 is added on NaCl and MnO2.

Q.505

What happens when K2MnF6 is reacted with SbF5.

Q.506

Halogen oxidises halide ions of higher atomic number. (True/False)

Q.507

In which state of halide ion F2 can act as an oxidising agent ?

Q.508

Which three elements do no reacts with hydrogen ?

Q.509

What happens when ? (a) Mg reacted with Br2 (b) P4 reacted with Cl2 (c) S8 reacted with F2 (d) Xe(g) reacted with F2

Q.510

What is the nature of chemical bond when a metal halide is found in its higher oxidation state ?

Q.511

Which of two is more covalent UF6 or UF4 ?

Q.512

What happens when

 → (i) CaF2 + H2SO4 con.   ∆

 → (ii) NaCl + H2SO4 conc.   ∆

Pt (as bijects) (iii) H2 + Br2   →

(iv) 2I2(s) + N2H4    → ∆

5731 K

 → (v) I2 + H2S   ∆ Q.513

How DCl can be prepared in laboratory.

Q.514

What do you call OCl–.

Q.515

How pure HOCl can be formed.

Q.516

What is house hold bleach.

Q.517

What happens when cold dil. NaCl is electrolysed ?

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IIT-JEE

INORGANIC PAPER

CHEMISTRY

P. JOY

Q.518

What is the composition of bleaching powder when Cl2 is passed over slacked lime.

Q.519

What happens when Ba(OH)2 is reacted with H2O2 & ClO2

Q.520

How HClO3 can be obtained by Ba(ClO2)2

Q.521

How Ba(ClO3)2 can be prepared. [What happens when Cl2 is passed through hot Ba(OH)2 solution]

Q.522

What happens when NaClO4 is reacted with conc. HCl.

Q.523

What is the major use of NH4ClO4 ?

Q.524

How NH4ClO4 can be obtained from NaClO4

Q.525

Inter halogen compounds are more reactive then halogens. Explain.

Q.526

Interhalogen compounds are always diamagnetic. Explain.

Q.527

Why interhalogen compounds have covalent character.

Q.528

Interhalogen compounds are conducts electricity. Explains.

Q.529

Why IBr known but ClBr is not known ?

Q.530

Which halogen forms largest inter halogen compounds.

Q.531

Which interhalogen compound exists in pentagonal bipyramidal geometry.

Q.532

Which halogen shows maximum oxidation state informing interhalogen compounds.

Q.533

The value of n in A Xn (interhalogen compounds) can be 1, 3, 5 or 7.

(T/F)

Q.534

A can never be F in A Xn (interhalogen compound)

(T/F)

Q.535

X can never be I in A Xn (interhalogen compound)

(T/F)

Q.536

A – X bond is weaker than A – A or X – X bond in A Xn (interhalogen compounds) (T/F)

Q.537

How many lone pairs are present on ClF3 molecule.

Q.538

What is Wij's reagent.

Q.539

What is Iodine number.

Q.540

Arrange the following interhalogen compounds in increasing order of reactivity IF, IF3, BrF, IF5, BrF3, ClF, IF2, BrF5, ClF3

Q.541

Why ICl3 exist in form of dimers (I2Cl6). Explain.

Q.542

What do you mean of cationic iodine. Give the examples of compounds showing existance of cationic iodine.

Q.543

Which acids are produced during hydrolysis of ICl.

Q.544

Which acids are produces during hydrolysis of BrF5.

Q.545

Complete and balance the following reactions : AlCl

3  → (i) I2 + ICl   ∆

→ (ii) CsF + IF7   ∆

Q.546

What is the general electronic configuration of elements of group 18.

Q.547

How many d electrons are present in Ne, Ar, Kr & Xe.

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IIT-JEE

INORGANIC PAPER

P. JOY

CHEMISTRY

Q.548

Why group 18 elements exhibit low chemical reactivity.

Q.549

Why noble gases have very low melting and boiling points ?

Q.550

Which noble gas has the lowest boiling point.

Q.551

Which noble gas has the unusual property of diffusing through rubber or glass.

Q.552

Which noble gas does not occur in the atmosphere.

Q.553

What is the total abundance by volume of noble gases in dry air.

Q.554

Which noble gas is the major component of total abundance of noble gases in dry air.

Q.555

Which noble gases constitutes the byproducts in liquefaction of air.

Q.556

What is the main commercial source of Helium.

Q.557

Which element is the second most abundant element in the universe.

Q.558

Which noble gas is obtained as the decay product of

Q.559

In which year real chemistry of noble gases began.

Q.560

Bartlett had noticed that PtF6 reacts with oxygen to form O2+ [PtF6]– & then he reasoned that PtF6 would react with xenon to form Xe+[PtF6]– what was the basis of his reasoning.

Q.561

Recent studies indicates that xenon reacts with PtF6 to form above indicated compound but it is to be formulated differently. What is its formula.

Q.562

Which type of elements (electronegative or electropositive) forms compounds with xenon.

Q.563

What are the gases evolved in the following chemical reaction : 2XeF2(s) + 2H2O(l) →

Q.564

Which noble gases are used in light bulbs designed for special purposes.

Q.565

Compounds of which noble gas have not been isolated but only identified by radiotracer tech-

226

Ra. Write a chemical reaction.

niques. Q.566

Which noble gases do not form true compounds.

Q.567

Which compound of krypton has been studied in detail.

Q.568

Which oxygen compound of xenon is formed when XeF4 undergoes hydrolysis write a balanced chemical equation.

Q.569

Complete the following reactions : Ni  → (i) Xe + F2  673K , 1atm

2:1

Ni Ni  → (iii) Xe + 3F   → (ii) Xe + 2F2  2 673K , 60 − 70 atm 673K , 5−7 atm

1:5

1 : 20

Q.570

Complete the following reaction : XeF6 + 3H2O →

Q.571

Which oxyacids are formed when XeF6 undergoes partial hydrolysis.

Q.572

Which oxide of xenon is a colourless explosive solid.

Q.573

Which oxyacid of xenon is a colourless volatile liquid.

Q.574

Which oxygen compounds of xenon has a square pyramidal and trigonal pyramidal molecular structure.

Q.575

Name the ion formed when XeO3 reacts with aq. alkali write a chemical reaction. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER

CHEMISTRY

P. JOY

Q.576

Ion formed above slowly disproportionates to give another ion. Name the ion.

Q.577

What is the oxidation state of Xe in perxenate ion.

Q.578

What is the colour of the solution of perxenate solutions.

Q.579

Perxenate solutions are powerful oxidising or reducing agents.

Q.580

Which noble gas species is isostructural with (a) ICl4– (b) IBr2– (c) BrO3–

Q.581

Which noble gas is used in filling balloons & why it is used.

Q.582

Which noble gas is used in discharge tubes and fluoresent bulbs for advertisement display purposes.

Q.583

Which noble gas is used in gas-cooled nuclear reactors.

Q.584

What are the three binary fluorides of xenon.

Q.585

Which fluoride of xenon has square planar structure.

Q.586

How many bonding pairs of e– are present in XeF6.

Q.587

Which fluoride of xenon have a distorted octahedral structure.

Q.588

Which ion forms bridges between XeF5+ units in the solid state of XeF6

Q.589

Which type of bridge is formed in solid state of XeF6.

Q.590

Which type of units are present in solid state of XeF6

Q.591

What is the shape of XeF5+ units present in solid state of XeF6

Q.592

Which species is formed when XeF4 react with SbF5. Give a chemical reaction : XeF4 + SbF5 →.

Q.593

At which temperature liquid He is used as cryogenic agent.

Q.594

Which noble gas has its application in NMR spectrometers.

Q.595

Which noble gas is radioactive in nature.

Q.596

State whether xenone fluoride are powerful flurinating agent.

Q.597

A compound gives off odourless, colourless gas with dil. HCl and develops golden gellone colour to flame compound is (a) NaNO3

(b) CaCO3

(c) Na2CO3

(d) Ca(NO3)2

Q.598

Li has higher I.E. than Na which of two is a better reducing agent ? Explain which factor is most responsible for above results ?

Q.599

Why Na is kept or stored in kerocene ?

Q.600

Why Li is not stored in kerocene ?

Q.601

Bright metallic lister of freshely cut piece of Na is lost on exposure to air why ?

Q.602

Which of the following does not react with Na metal ? (a) D2O

(b) C2H5OH

(c) Diethyl ether

(d) Acetone

(c) Na

(d) K

(c) Low O.P.

(d) High m.p., b.p.

M(g) → M+(g) + e– is most favourable in

Q.603

(a) Cs Q.604

(b) Li

Which is a characteristic of alkali metal (a) Conductivity

(b) High I.P.

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IIT-JEE

INORGANIC PAPER Q.605

P. JOY

CHEMISTRY

It same molar amount of lithium, sodium & potassium are dissolved in water and the heat released are measured Q1, Q2 & Q3. Which of the following relations are correct.

Li

Na

K

Q1

Q2

Q3

(a) Q1 > Q2 > Q3

(b) Q1 < Q2 < Q3

(c) Q1 = Q2 = Q3

(d) Q2 > Q1 > Q3

M + H2O → MOH + ½H2

Q.606

What is order of alkali metals reactivity. Q.607

Li reacts with water slowly but when added to water explodes why ? How thermodynamic and kinetic terms can be related to above observation.

Q.608

Does during the reaction of K with water K solid evaporates ?

Q.609

When alkali metals are added to water how does it changes the pH of water ?

Q.610

How does alkali metals react with limited quantity of oxygen ?

Q.611

What happens when alkali metal are reacted with excess of oxygen

Q.612

K(excess) + O2 → product is (a) KO2

(b) K2O

(c) K2O2

(d) None

Q.613

Which alkali metal can be used to absorb N2.

Q.614

Which elements are called S block elements ?

Q.615

Why I A group elements are called alkali metals ?

Q.616

Which alkali metal is most abundant in earth crust ?

Q.617

Why alkali metals are not found in free state ?

Q.618

What are Globular salt, salt cake, chilisalt peter ?

Q.619

What you call an element if it has 18e– in Penultimate shell and 1 electron in outer most shell ?

Q.620

What you call an element if it has 8e– in Penultimate shell and one e– in outermost shell ?

Q.621

Why do alkali metals show mealability, ductility, etc.

Q.622

Why alkali metal have weak metallic bond ?

Q.623

Why alkali metal have low m.p. as compared to Transition metals.

Q.624

Which alkali metal is a liq. at room temperature.

Q.625

What is unit cell type of alkali metals ?

Q.626

Why Cs is used in photoelectric cells ?

Q.627

Why general analytical techniques like coloured ppt, titrations optical rotation are not useful for alkali metal analysis ?

Q.628

Why alkali metals do not form coloured compounds.

Q.629

How do alkali metals are qualitatively identified ?

Q.630

What are colours imparted in flame by alkali metals ? VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER

P. JOY

CHEMISTRY

Q.631

Why alkali metals impart colour to bunsen flame.

Q.632

Why different alkali metals impart different colours to bunsen flames ?

Q.633

In flame why alkali metals or metal salt is added to HCl to prepare paste ?

Q.634

Why in flame test Cu wires cannot be used in place of Pt wire ?

Q.635

What is the reliability of flame test ?

Q.636

How the formation of various oxides of alkali metals can be related to their size ?

Q.637

What is structure of Li2O, Na2O, K2O, Rb2O.

Q.638

Why some alkali metals form oxide some form peroxide and other forms super oxide.

Q.639

A student wish to confirm a white solid as Na2O or Na2O2. He dipped red litmus paper into freshely prepared solution of water and found litmus decolouried, solid is (a) Na2O 2

(b) Na2O

(c) NaO2

(d) None

Q.640

What would have happened if red litmus has brought in contact with Na2O.

Q.641

What happens when following is added to water (a) Na2O

(b) Na2O

(c) KO2

Q.642

Which of following has highest bond order among O22–, O2–, O2, O2–

Q.643

Predict the magnetic nature of following ? (a) Na2O 2

(b) KO2

(c) O2

Q.644

What is oxone chemically ?

Q.645

What is the order of basic strength of following oxides ?

(d) Na2O

Li2O, Na2O, K2O, Rb2O, Cs2O Q.646

Why Na2O2 & KO2 are used in space ships.

Q.647

What are washing soda, heptahydrated sod. carbonate and crystalline carbonate, soda ash.

Q.648

Which elements of P.T. forms most stable carbonates ?

Q.649

→ What happens when Na2O   ∆

red hot

(a) H2O lost

(b) CO2 lost

(c) Na2O + CO2 formed (d) None

Q.650

Why alkali metal carbonates are stable on heating ?

Q.651

Arrange following in order of stability H2CO3, NaHCO3, Na2CO3

Q.652

What is the order of thermal stability of alkali metal carbonates ?

Q.653

Arrange following ions in order as indicated Li+, Na+, K+, Rb+, Cs+ (a) Ionic radii

(b) Hydrated radii

(c) Hydration number

(d) Hydration enthalpy

(e) Ionic mobility

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INORGANIC PAPER

CHEMISTRY

P. JOY

Q.654

What is the primary co-ordination of Li+ ion.

Q.655

In what order M+ ions eluted from cation exchange resins ?

Q.656

How would you make LiH ? Why is it more stable than NaH.

Q.657

How does change radius of Li+ differ from other alkali metal ion ?

Q.658

What other ion has properties similar to alkali metal ion ?

Q.659

The solubility of Li+ cation matches to which other cation.

Q.660

why Li3N is stable where as Na3N does not exist at 25ºC.

Q.661

Why lithium salts are commonly hydrated where as other alkali ions are anhydrous.

Q.662

For salts of strong acids the Li salt is usually the most soluble in water of the alkali metal salts, where as Li salts are usually less soluble than there of the other elements.

Q.663

What happens when Li2CO3 is strongly heated till 500ºC. (a) H2O vapours are formed

(b) H2O, Li2O, CO2

(c) Li2O, CO2 only

(d) None

Q.664

Why Li2CO3 decomposes on heating while other metal carbonates donot

Q.665

Alkali metal carbonates are good soluble in water. Explain why ?

Q.666

Why alkali metal carbonates are alkaline in nature ?

Q.667

What are the only five solid bicarbonates :

Q.668

Why Na2CO3 & CaCO3 differenting react on heating ?

Q.669

How will you make distinction between Na2O and Na2O2.

Q.670

What happens. When Li2CO3 & Na2CO3 are heated upto 500ºC.

Q.671

Why all bicarbonates decompose on heating.

Q.672

Comment on the solubility of bicarbonates ?

Q.673

Which of the two is more basic in Na2CO3, NaHCO3 ?

Q.674

What happens when Na2CO3 . NaHCO3.2H2O is strongly heated ?

Q.675

What happens when Na metal is added to highly pure liq. NH3 ?

Q.676

How does the blue colour of Na in NH3Cl, changes when Na is added in high concentration.

Q.677

Why solution of Na in NH3(l) appears Blue.

Q.678

Why do all alkali metals form same blue colour.

Q.679

Blue colour of solution of alkali metal in NH3 is due to (a) Na metal

(b) NaNH2

(d) Ammonated metal ion Q.680

What organic application of Na in NH3(l) ?

Q.681

Na+NH3(l) observation are

(c) Ammonated e– (e) NaLi

(a) Blue colour

(b) Strong reducing agent

(c) Produce NaNH2

(d) Produce H2

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INORGANIC PAPER

P. JOY

CHEMISTRY

Q.682

Blue solution of alkali metals in NH3(l) is diamagnetic or paramagnetic ?

Q.683

How blue solution of alkali metal ion is decomposed ?

Q.684

What happens if NH3(l) is carefully evaporated from blue solution ?

Q.685

To blue solution of Na/NH3(l) if more sodium is added it show metallic copper coloured solution then its paramagnetism is (a) Increased

(b) Decreased

(c) The same

(d) No change

Q.686

Why paramagnetism of blue solution decreases on increasing concentration.

Q.687

Which other liq. form blue colour other than NH3(l) (a) THF

(b) HMPA

(d) RNH2

(e) Ethers

(c) Diglyme

Q.688

Which alkali metals is radioactive.

Q.689

Which isotope of Fr has longest life.

Q.690

What is the half life of longest lived isotope of francium.

Q.691

How many valence electron(s) are present in the alkali metal.

Q.692

Which type of ion (monovalent or bivalent) are formed by the alkali metal.

Q.693

Superoxides are paramagnetic or diamagnetic is nature.

Q.694

Which oxide of alkali metal is widely used as an oxidizing agent in inorganic chemistry.

Q.695

Give the reason for the low solubility of LiF & CsI in water.

Q.696

Why alkali metals forms salts with all the oxoacids.

Q.697

Which alkali metal have thermally unstable carbonate.

Q.698

Li, Na, K, Rb, Cs (increasing order of occurence in lithosphere)

Q.699

Li, Na, K, Rb, Cs (increasing order of ionization enthalpy).

Q.700

Li, Na, K, Rb, Cs (Increasing order of metallic radius)

Q.701

Li, Na, K, Rb, Cs (Increasing order of ionic radius).

Q.702

Li, Na, K, Rb, Cs (Increasing order of melting point).

Q.703

Li, Na, K, Rb, Cs (Increasing order of boiling point).

Q.704

Li, Na, K, Rb, Cs (Increasing order of density)

Q.705

Li, Na, K, Rb, Cs (Increasing order of standard potential).

Q.706

Cs2CO3, Rb2CO3, K2CO3, Na2CO3, Li2CO3 (increasing order of stability of carbonates)

Q.707

CsHCO3, RbHCO3, KHCO3, NaHCO3, LiHCO3 (increasing order of stability of bicarbonates)

Q.708

MCl, MBr, MF, MI (Increasing order of covalent character) (M = alkali metal)

Q.709

KCl, KBr, KI (Decreasing solubility in water)

Q.710

LiF, NaF, KF, RbF, CsF (Increasing order of lattice energy)

Q.711

Li, Na, K (Decreasing order of reducing nature in solution).

Q.712

LI2O, Na2O, K2O, Rb2O < Cs2O (Increasing order of basic nature) VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER

CHEMISTRY

P. JOY

Q.713

Li, Na, K, Rb, Cs (Increasing order of reactivity with water)

Q.714

Li, Na, K, Rb, Cs (Increasing order of electropositive character).

Q.715

Write the chemical formula of epsomite.

Q.716

Why Mg does not react with oxygen & water.

Q.717

Which gas is liberated from H2O by magnesium amalgam.

Q.718

Which oxide and nitride are formed when Mg burns in air.

Q.719

Which organometallic compound is formed when alkyl & aryl halides react with Mg.

Q.720

Magnesium acts as a (oxidising or reducing agent) in the production of metals such as Ti, Zr and Hf.

Q.721

Which alkaline earth metal is used as a an oxygen scavenger and for cathodic protection of other metals.

Q.722

Why the temperature of 1273 k is maintained when lime stone is heated for the production of quicklime.

Q.723

What is another name of calcium oxide.

Q.724

What is slaking ?

Q.725

Quicklime slaked with soda gives a solid.

Q.726

Complete the following chemical reaction occuring at high temperature (a) CaO + SiO2 → (b) CaO + P4O10 →

Q.727

What is slaked lime & how it is produced.

Q.728

What is lime water ?

Q.729

Suspension of slaked lime in water is known as.

Q.730

What happens when CO2 is passed through lime water.

Q.731

Identify X in following reaction Ca(OH)2 + CO2 (excess)



X (soluble)

Q.732

Milk of lime reacts with chlorine and forms a compound A which is a constituent of bleaching powder. Identify the compound A.

Q.733

What is gypsum.

Q.734

How plaster of paris is obtained.

Q.735

Why compounds of alkaline earth metal are less ionic than the corresponding compounds of the alkali metals.

Q.736

Which type of bond (ionic or covalent) is found in BeO.

Q.737

Arrange the following in order of their indicated property. (i) Mg(OH)2, Sr(OH)2, Ba(OH)2, Ca(OH)2 (Solubility) (ii) Ca(OH)2, Ba(OH)2, Sr(OH)2, Mg(OH)2 (Basic character)) (iii) Mg(OH)2, Co(OH)2, Sr(OH)2, Ba(OH)2 (Solubility) VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER

IIT-JEE

CHEMISTRY

P. JOY

Q.738

Name the ion formed when Be(OH)2 reacts with alkali. Give the chemical reaction

Q.739

How many halogen atoms are coordinated with Be in condensed phase of beryllium halides.

Q.740

Which halides of magnesium are soluble in organic solvents.

Q.741

Fluoride of which alkaline earth metal is known as fluorospar.

Q.742

Name the halide of the alkaline earth metal which is the only large scale source of fluorine.

Q.743

Arrange the following : (i) BeCO3, MgCO3, CaCO3,SrCO3, BaCO3 (Thermal stability) (ii) CaSO4, SrSO4, BaSO4 (Solubility) (iii) Ca(C2O4)2, Sr(C2O4)2, Ba(C2O4)2 (Solubility)

Q.744

Nitrate of which alkaline earth metal crystallizes as the anhydrous salt.

Q.745

Complete the following reaction ∆ 2Ca(NO3)2   →

Q.746

Name the nitrate of alkaline earth metal which is used in pyrotechnics for giving red flame.

Q.747

Why the sulphates of Be & Mg are readily soluble.

Q.748

Except Be, remaining members of the group 2 can have a coordination number of six. Why it is so ?

Q.749

Name the minerals in which Mg occurs in earth's crust.

Q.750

How Mg is obtained from magnesite or dolomite.

Q.751

Consider the following reaction CaCO3.MgCO3 + 2H2SO4   → CaSO4 + MgSO4 + 2H2O + 2CO2 How the two sulphates formed in above reaction can easily be separated.

Q.752

What is the chemical formula of magnesium sulphate which is obtained from the solution containing CaSO4 & MgSO4 is the temperature range 273-320K.

Q.753

What is the correct formulation of the heptahydrate form of magnesium.

Q.754

What is pottash magnesis & what is its chemical composition.

Q.755

Give an medical application of magnesium sulphate.

Q.756

What are the important compounds present in portland cement.

Q.757

Why portland cement was named so ?

Q.758

Who firstly used the name portland cement ?

Q.759

Chemically explain the setting of cement.

Q.760

Which element of group 2 is not known as the alkaline earth metal.

Q.761

How many valence electrons are present in Mg.

Q.762

Which shell occupies valence electrons in Ba.

Q.763

Which metals (alkali or alkaline earth) have smaller atomic radii. Give reason in support of your answer. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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IIT-JEE

INORGANIC PAPER Q.764

P. JOY

CHEMISTRY

The first ionization enthalpies of alkaline earth metals are higher than these of alkali metals but second ionization enthalpies of the alkaline earth metals are smaller than those of corresponding alkali metals why.

Q.765

Which alkaline earth metals do not give flame test & why.

Q.766

Which alkaline earth metal imparts apple green colour to the flame.

Q.767

When KCN is added to CuSO4 solution which complex is formed.

Q.768

Out of AgNO3, AgF and AgClO4 which salts are water soluble.

Q.769

Write the stability of Cu+ and Ag+ halide complexes are in increasing order.

Q.770

Most commen oxidation state of lanthanides is.

Q.771

The purest form of Fe is

Q.772

Cu+ is diamagnetic explain.

Q.773

Paramagnetism is given by the relation µ = 2 s(s + 1) megnetons where 's' is the total spin. On the this basis what is the paramagnetism of Cu+ ion.

Q.774

What is gun metal.

Q.775

An acidic solution contain Cu+2, Pb+2, Zn+2. If H2S gas is passed through this solution, which of the ppt out.

Q.776

Silver ornaments turn black in atmosphere. Which gas is responsible.

Q.777

In dilute alkaline KMnO4 solution MnO4– changes to.

Q.778

What is d-d transition.

Q.779

AgCl and Nacl are colourless while AgBr and AgI are coloured. Explain.

Q.780

Why d-block element have ability of complexes formation.

Q.781

What happens when H2O2 is added to an acidified solution of K2Cr2O7

Q.782

Which metal of 3d transition series have maximum oxidation state.

Q.783

Arrange the following hydroxy compounds in order of increasing acid strength, and account for the trend : (a) CrO2(OH)2

(b) Cr(OH)2

(c) Cr(OH)3

Q.784

Explain how Cr(OH)3 can act both as an acid and as a base.

Q.785

Why does chromium seem to be less reactive than its standard reduction potential suggests ?

Q.786

[FeIII(CN)6]3– ion has magnetic moment of 1.73 B.M., while [Fe(H2O)6]3+ has a magnetic moment of 5.92 B.M. Explain.

Q.787

What is the EAN (effective atomic number) of the underlined atoms in the following complexes ? (a) [Fe(CN)6]4–

Q.788

(b) [Cr(en)3]3+

(c) Ni(CO)4

Match the geometry (given in column A) with the complexes (given in column B) in : A

B

(I)

Octahedral

(a) [Ni(CN)4]2–

(II)

Square planar

(b) [Fe(CN)6]4–

(III)

Tetrahedral

(c) Ni(CO)4

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IIT-JEE

INORGANIC PAPER Q.789

CHEMISTRY

P. JOY

One mol of the aqueous solution of the complex CoCl3.5H2O when treated with excess of aqueous AgNO3 solution gave one mol of white ppt of AgCl. What is the complex ? (For this you should know that how many Cl– ions are not coordinated to Co3+ - naturally one which is precipitated as AgCl)

Q.790

Arrange [Fe(CN)6]4–, [Fe(CN)6]3–, [Ni(CN)4]2– and [Ni(H2O)4]2+ in increasing order of magnetic moment.

Q.791

Magnetic of Fex+ ion is

35 B.M. Determine number of unpaired electrons. Also write its elec-

tronic configuration. Q.792

s- and p-block elements form coloured/colourless ? (a) Zn2+

(b) Cu+

(c) Cu2+

(d) Sc3+

(f) V3+

(g) Mn2+

(h) Ni2+

(i) Na+

(e) Ti2+ (j) Ca2+

Q.793

Hg2+ salts are colourless. Explain.

Q.794

Compounds, containing the Sc3+ ion are colourless, whereas those containing the Ti3+ ion are coloured. Explain.

Q.795

Explain the term 'Lanthanide contraction'.

Q.796

Due to 'lanthanide contraction', second and third row transition elements (called 4d and 5d series respectively) have similar radii. What are the other properties do you think would be similar ?

Q.797

Reduction using Lindlar catalyst converts 2-butyne into ....

Q.798

TiCl4 is used as ........... catalyst in polymerisation of ethylene.

Q.799

Cracking of hydrocarbons in presence of hydrogen is done by ............ catalysts.

Q.800

VO2+ is oxidised to VO2+ by MnO4– in acidic medium, which in turn is reduced to Mn2+. Write balanced equation for this reaction.

Q.801

One of the following oxide is also called chromic acid. Select that one : CrO2, Cr2O3, CrO3, CrO.

Q.802

What is oxidation number of Cr in CrO2Cl2.

Q.803

What is oxidation number of Cr in CrO5 or CrO(O2)2

Q.804

What is oxidation number of Cr in (NH4)2Cr2O7

Q.805

What is oxidation number of Cr in [Cr(O2)4]3–

Q.806

Arrange the following ions in order of increasing strength as a reducing agent, and account for the trend : (a) Cr2+

(b) Cr3+

(c) Cr2O72–

Q.807

H2O 2 can be oxidised to O2 by MnO4– in acidic as well as in basic medium. Write reactions

Q.808

What happens when CO2 gas is passed into MnO42– solution ?

Q.809

Unreacted AgBr in photography is removed by hypo used as 'fixer'. What is the reaction ?

Q.810

(a) When H2S gas is passed into FeCl3 solution, yellow colour of FeCl3 changes to light green. Explain (b) Same behaviour is also observed when SnCl2 solution is observed. Explain.

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CHEMISTRY

P. JOY

Q.811

Given chemical tests for making distinction between Fe2+ and Fe3+ ions.

Q.812

When K2HgI4 reacts with NH3, brown ppt is formed. Explain the formation of brown ppt.

Q.813

What is brass.

Q.814

What is coinge metal

Q.815

What is nichrome.

Q.816

Name those anions which have high solubility

Q.817

Which anion has least ppt. test.

Q.818

Soda extract is prepared by which carbonate.

Q.819

Soda extract can't be used for which anion detection.

Q.820

Name effervetive gas.

Q.821

Which anions release gases which turns lime water milky.

Q.822

The milkiness of lime water is due to.

Q.823

Formula of lime water is.

Q.824

Mikiness of lime water dissappears due to formation of x on passage of excess CO2 X is.

Q.825

Which gas has suffocating order and responds to litmus paper.

Q.826

What is the colour of K2Cr2O 7 paper when it is treated with SO2.

Q.827

What is the oxidation state of chromium when it is reduced by SO2.

Q.828

In which medium di-chromate ions are converted into chromate ion.

Q.829

Which of the 2 has more oxidising action dichromate or chromate.

Q.830

Which type of substances are detected by potassium iodide starch paper.

Q.831

Which type of reagents are detected by KIO3 starch paper.

Q.832

What happens when white ppt. of Ba(CO3) is is treated with dil acid.

Q.833

Out of CO32, SO3–, Br–, I–, Cl– whose barium salts or silver salts are dissolved by dil. acids.

Q.834

In which case CrO2Cl2 test can't be employed.

Q.835

Which cation should be absent when CrO2Cl2 test is employes.

Q.836

Which anion other than halide should be absent when CrO2Cl2 chloride test is employed.

Q.837

What happens when NaCl is treated with potassium dichromate ?

Q.838

Chromyl chloride formation indicates formation of which gas.

Q.839

What is formula of chromyl chloride and its color.

Q.840

What is the gas released when Cl– ions are added with conc. H2SO4.

Q.841

What is the gas evolves with Cl– ions are reacted with MnO2.

Q.842

Which of the 2 gases Cl2 or HCl is coloured.

Q.843

What happens when chromyl chloride gas is passed into alkaline water.

Q.844

What happens when chlorides are added to AgNo3. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER

IIT-JEE

CHEMISTRY

P. JOY

Q.845

Name some substances in which AgCl is soluble.

Q.846

Which of the Ag halide is most colored.

Q.847

Which theory explains colour of Ag halides.

Q.848

Which Ag halide is most easy to break by NH3 solution.

Q.849

Which halide ions on addition of concentration H2SO4 does not evolve halogen.

Q.850

How does solubility of PbCl2 depends on the temp. of water.

Q.851

Name one acid which on added to Br– and I– does not evolves halogen.

Q.852

Which liq. can be used for organic layer test.

Q.853

What is the colour of organic layer when Br – and Cl– are tested separately.

Q.854

Which oxidising agent can theoretically employed as for organic layer test of halides.

Q.855

What happens when Br– ions are reacts PbO2.

Q.856

Name some reagents which can oxidise Br– into bromine.

Q.857

Which halogen can displace bromide from its salt.

Q.858

When iodide is added to conc. H2SO4 which vapor and gas are released.

Q.859

Which hydrogen halide among HCl, HBr, HI can reduce H 2SO4 into SO2.

Q.860

When iodides are treated with H2SO4 acid, a yellow ppt. and rotten egg smell are produced, small is due to.

Q.861

Which halide ion can't be oxidised by MnO2.

Q.862

What happens when CuSO4 is added to iodide.

Q.863

What happens when hypo is added to I– ion.

Q.864

What is formula of Nesslers reagent.

Q.865

What happens when HgCl2 is added to excess of KI.

Q.866

Which halide ion catalyses reaction between Ce4+ and aresnate ion.

Q.867

What happens when I– ions are treated with acidified potassium nitrite solution.

Q.868

Which gas is coorless but on exposure to air turns brown.

Q.869

Which gas is complexed by FeSO4 to produce brown solution.

Q.870

What is oxidation state of Fe in brown ring test.

Q.871

Which metals or heating with NO3– evolves NH3 gas.

Q.872

Which anions show brown ring complex with FeSO4.

Q.873

Which gas is evolved when NO3– is decomposed by conc. H2SO4

Q.874

What happens when NO2– are treated with dil. H2SO4.

Q.875

What is the colour of HNO2.

Q.876

Which gas is evolved when NO3– are reduced by Cu turning.

Q.877

Which of the 2 is soluble in HCl on warming BaSO4 or Ba3(PO4)2

Q.878

What happens when BaSO4 ppt is reduced by charcoal in presence of Na2CO3. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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CHEMISTRY

P. JOY

Q.879

Write some common sulphate which are insoluble.

Q.880

What is the formula of ppt. formed when SO42– are treated with mercuric nitrates.

Q.881

What is the formula of ammonium molybdate.

Q.882

What is the formula of ammonium molybdate that is commercially available.

Q.883

Formula of ammonium phosphomolybdate.

Q.884

What is the color of ammonium phosphomolybate.

Q.885

What happens when disodium hydrogen phosphate is added to FeCl3.

Q.886

What happens when ZrO(NO3)2 is added to phosphate ions.

Q.887

Which ions on treatment with ammonium molybdate produce canary yellow colour.

Q.888

What are the gases produced when C2O42– is reacted with conc. H2SO4.

Q.889

What is the colour of flame when CO is burnt.

Q.890

What happens when drops of potassium per mangnate is added to oxalate ion solution.

Q.891

What is the colour change produce when potassium dichromate is added to aq. solution of C2O42– ion.

Q.892

Which anion has a smell of vinegar.

Q.893

What happens when CH3COO– are rubbed with oxalic acid.

Q.894

Name one substance which is an acetate and insoluble.

Q.895

Which anion show fruity ester test.

Q.896

Which reagent or addition to CH3COO– forms blood red calouration.

Q.897

What is the formula of blood red coloration formed in above test.

Q.898

What is the formula of basic ferric acetate.

Q.899

Which anion other than CH3COO– forms blood red coloration and then brown ppt on heating.

Q.900

Which anion on reaction with KMnO4 undergoes O2 catalysis.

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SOLUTIONS Q.1 1. 2Al + 3O2 → Al2O3 2. 2Al + N2 → 2AlN 3. 2Al + 3Cl2 → 2AlCl3 4. Al + Cr2O3 → Al2O3 + Cr 5. Al + Mn3O4 → Al2O3 + Mn 6. Al + HCl → AlCl3 + H2 ↓H2O Al(OH)3 + 3HCl 7. 2Al + 3H2SO4(dil) → Al2(SO4)3 + 6H2 8. 2Al + H2SO4(conc.) → Al2(SO4)3 + SO2 + H2O 9. Al + HNO3 → No reaction 10. Al + NaOH → Al(OH)3 +

3 H 2 2

High Temp. 11. 2Al + AlCl3   → 3AlCl

Q.2 1. Al(OH)3 + 3H+ → Al+3 + 3H2O acid 2. Al(OH)3 + NaOH → Na[Al(OH)4] or NaAlO2.2H2O base

sodium meta aluminate

Below 450º C 3. Al(OH)3   → Al2O3 (α-form) Above 450º C 4. Al(OH)3   → Al2O3 (γ-form)

Q.3

M(I) M'(III) (SO4)2.12H2O

Q.4

6 water molecule act as ligands about mono valent metal cations and 6 water molecule act as ligands about trivalent metal cations.

Q.5

Almost any unipositive cations (except Li+) most commen alums have K+, NH4+

Q.6

Al+3, Ti+3, V3+, Cr3+, Fe3+, Mn3+, Co3+, Ga3+, Re3+, Ir3+

Q.7

Due to different type of ions.

Q.8

Li+

Q.9

It loses water of crystallisation and swell up.

Q.10

Alums are used as mordant in dyeing.

Q.11

Acidic due to cationic hydrolysis of trivalent cation. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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Q.12

An aqueous solution containing equimolar amount of Al2(SO4) and K2SO4 crystallises as allums.

Q.13

Double dulphate of divalent ions and trivalent ions with 24 water molecules in their crystals are known as pseudo alums.

Q.14

No

Q.15

Al2SO4.18H2O

Q.16

Al(OH)3 + 3H+ → Al+3 + 3H2O acid Al(OH)3 + NaOH → Na[Al(OH)4] or NaAlO2.2H2O base

sodium meta aluminate

Al(OH)3 → Gelatinous white ppt.

Q.17

Zn(OH)2 → white ppt. Q.18

It is prepared by passing dry chlorine over aluminium powder.

Q.19

Al2O3 + 3C + 3Cl2 → 2AlCl3 + 3CO

Q.20

In inert orgnic solvent and in vapour state.

Q.21

The high enthalpy of hydration is sufficient to break the covalent dimer into [M(H2O)6]3+ and 3X– ions.

Q.22

Yes

Q.23

Acidic, AlCl3 + 3H2O → Al(OH)3 + 3HCl

Q.24

Yes

Q.25

It is hydroscopic in nature.

Q.26

AlCl is unstable below 800ºC. It disproportionate below 800ºC 3AlCl → AlCl3 + 2Al

Q.27

AlCl3 + Cl– → [AlCl4]–

Q.28

Al2Cl6 + LiH (excess) →Li[AlH4]

Q.29

Al2O3

Q.30

α-Al2O3, β-Al2O3

Q.31

α-Al2O3

Q.32

Al + Fe2O3 → Al2O3 + Fe + heat

Q.33

2Al2O3 + 2AlCl3 → 6AlCl + 3O2

Q.34

α-form

Q.35

γ-Al2O3

Q.36

The strength of C–C bond is very high.

Q.37

Pb

Q.38

Graphite

Q.39

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Q.40

Pb

Q.41

Free electrons present in 2p orbitals of graphite

Q.42

Graphite

Q.43

C

Q.44

α-Quartz ⇔ β-Quartz ⇔ Tridymite

Q.45

α-Sn ⇔ β-Sn

Q.46

α-Sn ⇔ β-Sn

Q.47

The conversion of white tin (β-Sn) is accompainied by an increase in volume and the letter, being

840

15ºC

160ºC

15ºC

160ºC





1600ºC



cristobalite

Rhombic Sn

Rhombic Sn

very brittle, easily crumbles down to powder, this phenomenon is known as tin disease. Q.48

When bent the metal produces a cracking sound due to rubbing of crystals over one another is known as tin cry.

Q.49

Sn

Q.50

Diamond

Q.51

CO, CO2, C3O2

Q.52

H2CO3

Q.53

HCOOH

Q.54

Fullerens are produced by evoparation of graphite by lesser.

Q.55

Yes

Q.56

60

Q.57

Purple colour

Q.58

Red orange colour

Q.59

Socker's ball

Q.60

Malonic acid

Q.61

CO2

Q.62

SnO

Q.63

CO

Q.64

CO → neutral, others → acidic

Q.65

SiO2

Q.66

Produce strong base by hydrolysis.

Q.67

1300ºC CaC2 + N2    → CaCN2

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INORGANIC PAPER Q.68

CHEMISTRY

P. JOY

HOH CaCN2    → Ca(OH)2 + H2N – CN

BH O 2

H2N − C − NH2 || O urea Coke

Q.69

→ CaCl + NaCN + N CaCN2 + 2NaCl   2 2 ∆

Q.70

∆ K4Fe(CN)6   → 4KCN + Fe + N2

Q.71

2KCN + H2SO4 → 2HCN + 2K+ + SO4–2

Q.72

Alkaline

Q.73

O2 HCN   → N ≡ C – C ≡ N 2+

Cu HCN   → Cu(CN)2 + NaCN Ag HCN   →

Cl2 + NaOH → OCl+ + Cl–

Q.74

(CN)2 + NaOH → OCN+ + CN– both produced similar type of ions. Q.75

SiO2 does not have tendency of pπ-pπ overlapping.

Q.76

CO2, SiO2 Acidic GeO2, SnO2 Amphoteric PbO2 Basic

Q.77

∆ Pb(NO3)2    → PbO + NO2

Q.78

CO2

Q.79

Gives mellitic acid [C6(COOH)6] and oxalic acid.

Q.80

(R2SiO)n

Q.81

Silicones are produced.

Q.82

sp3

Q.83

β-Quartz

Q.84

Silicates are formed

Q.85

2KOH + SiO2 → K2SiO3 + H2O CaCO3 + SiO2 → CaSiO3 + CO2 2KNO3 + SiO2 → K2SiO3 + 2NO2 + ½O2 SiO2 + 6HF → H2SiF6 + 2H2O C + SiO2 → CO2 + Si

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Q.86

Flint

Q.87

Super cooled liquid, pseudo solid.

Q.88

SiO2 + 6HF → H2SiF6 + 2H2O

Q.89

Fluoro siliclic acid.

Q.90

Na2SiO3.CaSiO3.HSiO2

Q.91

Na2SiO3.H2O

Q.92

When transition metals are added into soda glass solution. Different type of colour are obtained.

Q.93

Silanes Sin H2n + 2 German Gen H2n + 2

Q.94

Vertex of silica is formed.

Q.95

Si + 2NaOH → NaSiO3 + H2↑

Q.96

HF

Q.97

Silanes

Alkanes

Toxic

Not

Autocombust

Not

Reducing agent

Not

Unstable

Stable

Q.98

KNO3 + SiO2 → K2SiO3 + 2NO2 + ½O2

Q.99

HF

Q.100

Corundum (α−Al2O3) and Carborundum (SiC)

Q.101

Glass

Q.102

SiO2

Q.103

Soda glass

Q.104

Hard glass

Q.105

SiO4–4, BO3–3

Q.106

Flint glass

Q.107

Stops U.V. light

Q.108

Pyrex glass

Q.109

∆ CaCO3 + Na2CO3 + SiO2 + H3BO3   → borosilicate gass

Q.110

Trimethyl amines sp3, Trisilyl amine sp2 hybridization

Q.111

N(CH3)3

Q.112

Polymeric organocompounds contain Si–O–Si bonds therefore known as silicones.

Q.113

SiO2 form

Q.114

C does not have 3d orbitals. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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Q.115

Tin is purifyed by electrolytic method

Q.116

Both SnO and SnO2

Q.117

∆ SnC2O4    → SnO + CO + CO2

P. JOY

Oxidation of SnO to SnO2 is checked by CO NaOH SnO2   → Na2SnO3

Q.118

H2SO 4 SnO2   → H3SnO3 stannic acid

Q.119

∆ SnCl2.2H2O   → Sn(OH)Cl

Q.120

SnCl4

Q.121

SnCl4.5H2O

Q.122

SnCl2.2NH3

Q.123

SnCl4.4NH3

Q.124

HgCl2 + SnCl2 → Calamel

Q.125

SnF2

Q.126

Does not reacts with organic acids.

Q.127

3SnCl2 + 2AuCl3 → 3SnCl4 + 2Au

Q.128

H2O 3SnCl2 + 2AuCl3 → 2Au+ + 3SnCl4   → Sn(OH)4

Q.129

H2O SnCl4.5H2O   → Sn(OH)Cl

Butter of Tin Q.130

Sn + HNO3 → H3SnO3

Q.131

SnI4 → yellow, SnCl4 and SnBr4 coloured

Q.132

SnO + 2HF → SnF2 + H2O

Q.133

Pb has more value of ionization energy then Sn due to poor shielding of the valence shell electrons by the electrons present in d and f subshells.

Q.134

PbO, PbO2, Pb2O3, Pb3O4

Q.135

Because Pb+2 is more stable than Pb+4

Q.136

Absence of d-orbitals in C

Q.137

C > > Si > Ge > Sn > Pb

Q.138

Three

Q.139

Fajan's rule VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER Q.140

IIT-JEE

CHEMISTRY

P. JOY

(a) C < Si < Ge < Sn < Pb (b) M.P., C > Si > Ge > Pb > Sn B.P., C > Si > Ge > Sn > Pb (c) Si < C < Ge < Sn < Pb (d) C > Si > Ge > Pb > Sn (e) C(+4), Si(+4), Ge(+4), Sn(+4), Pb(+2) Group V elements have ns2-np3 general configurator which is a half filled orbital having extra

Q.141

stability. So they have high I.E. Q.142

As and Sb

Q.143

The bond strength between Bi-Bi is quite poor and secondly due to inert pair effect, it has poor tendency to form more no. of bonds with other Bi atoms.

Q.144

+3 and +5

Q.145

NH3(–3), NH2-NH2(–2), NH2OH(–1), N2(0), N2O(+1), NO(+2), N2O3(+3), NO2(+4), N2O5(+5)

Q.146

Group V elements have poor bond strength between their atoms.

Q.147

H−N=N=N

Q.148

N2

Q.149

Red, yellow, black.

Q.150

White and yellow

Q.151

White and yellow

Q.152

Nitrogen

Q.153

N2 has high bond energy.

Q.154

Nitrogen N2 others M4

Q.155

pπ -dπ

Q.156

H2O Ca3, N2   → NH3

+



H2O Ca3P2 :   → PH3

Ca3P2 + 6HOH → 3CO(OH)2 + 2PH3 phosphene

Q.157

Ca3N2 + 6H2O → 3Ca(OH)2 + 2NH3 Zn3As2 + 6H2O → 3Zn(OH)2 + 2AsH3 Q.158

Hydrazine

Q.159

NH3 > PH3 > AsH3 > SbH3

Q.160

NH3 > PH3 > AsH3 > SbH3 > BiH3

Q.161

BiH3

Q.162

NH3

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Q.163

NH3 has H-bonding.

Q.164

NH3 > PH3 > AsH3 > SbH3 > BiH3

Q.165

BiX3

Q.166

Pyramidal

Q.167

PCl3 + HOH → H3PO3 + 3HCl

Q.168

NX3

Q.169

Yes

Q.170

Nitrogen

Q.171

Trihalides are more stable

Q.172

Yes

Q.173

Gaseous state PCl5 and in solid state [PCl4+] [PCl6–]

P. JOY

Q.174

Q.175

Ca(PO4)2 + C → CaCO3 + P

Q.176

Yellow

Q.177

Yellow P

Q.178

Red P

,

Q.179

Q.180

Yellow

Q.181

(a) White P converts into Red P (b) White P appears yellow

Q.182

Polymeric structure.

Q.183

Insoluble Red water P

Q.184

P + Ca or Mg → Ca3P2 or Mg3P2 P + Na or K → Na3P or K3P

Q.185

Highly reactive, burshing into Hames when exposed to air. VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER Q.186

O2 P  → P2O3

Q.187

PH3 & NaH2PO2

Q.188

Reducing agent

Q.189

P + HNO3 → H3PO4 + NO2

IIT-JEE

CHEMISTRY

P. JOY

P + Conc H2SO4 → H3PO4 + SO3 P + CuSO4 → Cu3P3 P + AgNO3 → Ag3P2 + HNO3 Q.190

PCl5 P   → PCl5 S8 P  → P4S3

Q.191

White

Q.192

(a) Ca3P2 + 6H2O → 3Ca(OH)2 + 2PH3 (b) Na3P + H2O → NaOH + PH3

Q.193

H2O AlP   → PH3 ↑ + Al(OH)3

Q.194

∆ H3PO3   → PH3 + H3PO4

Q.195

P4 + 3NaOH + 3H2O → PH3 + 3NaH2PO2

Q.196

Ring of N2O5 are known as vertex ring. During formations of PH3, PH3 is oxidized by O2 and forms P2O5

Q.197

P4 + NaOH → Na2HPO4 + PH3↑ PH3 + O2 → HPO3 PH3 + O2 → P2O5 + H2O vertex ring

Q.198

N has no d-orbital thus it can't accept H2O as a ligand for hydrolysis.

Q.199

Due to high P – F bond strength

Q.200

H2O NCl3   → X H2O PCl3   → H3PO3 H2O AsCl3   → As2O3 H2O SbCl3   → Sb OCl H2O BiCl3   → BiOCl

Q.201

Bi does not show +5 oxidation state due to inert pair effect.

Q.202

B > Al < Ga > In < Tl

Q.203

BF3 < BCl3 < BBr3 < BI3 VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER Q.204

BCl3 < AlCl3 < GaCl3 < InCl3

Q.205

B2O3 < Al2O3 < Ga2O3 < In2O3 < Tl2O3

Q.206

B > Al > Ga > In > Tl

Q.207

Ga < In < Tl

Q.208

B > Al > Ga > In > Tl

Q.209

Al > Ga > In > Tl

Q.210

C > Si > Ge > Sn < Pb

Q.211

C >> Si > Ge > Sn > Pb

Q.212

C > Si > Ge > Sn > Pb

Q.213

PbF2 > PbCl2 > PbBr2 > PbI2

Q.214

Si < C < Ge < Sn < Pb

Q.215

N < P < As > Sb > Bi

Q.216

N < P < As < Sb > Bi

Q.217

NH3 > PH3 > AsH3 > SbH3 > BiH3

Q.218

NH3 < PH3 < AsH3 < SbH3 < BiH3

Q.219

PH3 < AsH3 < NH3 < SbH3

Q.220

NI3 > NBr3 > NCl3 > NF3

Q.221

NH3 > PH3 > AsH3 > SbH3 > BiH3

Q.222

PCl3 > AsCl3 > SbCl3

Q.223

N2O3 > P2O3 > As2O3

Q.224

N2O5 > P2O5 > As2O5 > Sb2O5 > Bi2O5

Q.225

N2O < NO < N2O3 < N2O4 < N2O5

Q.226

P2O5 > As2O5 > Sb2O5 > N2O5 > Bi2O5

Q.227

NCl3 > PCl3 > AsCl3 > SbCl3 > BiCl3

Q.228

PF3 > PCl3 > PBr3 > PI3

Q.229

PI3 > PBr3 > PCl3 > PF3

Q.230

HNO3 > H3PO4 > H3AsO4 > H3SbO4

Q.231

O < S > Se > Te

Q.232

O > S > Se > Te > Po

Q.233

H2O < H2S < H2Se < H2Te

Q.234

H2Te < H2Se < H2S < H2O

Q.235

H2O > H2S > H2Se > H2Te

Q.236

H2O < H2S < H2Se < H2Te

Q.237

H2O > H2S > H2Se > H2Te

Q.238

SO3 > SeO3 > TeO3

IIT-JEE

CHEMISTRY

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P. JOY

Q.239

SO > SO2 > SO3

Q.240

H2TeO3 < H2SeO3 < H2SO3

Q.241

F < Cl > Br > I

Q.242

F > Cl > Br > I

Q.243

Cl2 > Br2 > F2 > I2

Q.244

F2 > Cl2 > Br2 > I2

Q.245

HI > HBr > HCl > HF

Q.246

HI > HBr > HCl > HF

Q.247

HF > HI > HBr > HCl

Q.248

H—F > H—Cl > H—Br > H—I

Q.249

HClO4 > HClO3 > HClO2 > HClO

Q.250

HClO > HBrO > HIO

Q.251

HClO3 < HBrO3 < HIO3

Q.252

HClO4 > HClO3 > HClO2 > HClO

Q.253

HClO > HBrO > HIO

Q.254

HClO4 < HClO3 < HClO2 < HClO

Q.255

MF > MCl > M—Br > MI

Q.256

I– < I3– < I3+ < I2O5 < H5IO6

Q.257

HClO < HClO2 < HClO3 < HClO4

Q.258

HI < I2 < ICl < HIO4

Q.259

He < Ne < Ar < Kr < Xe

Q.260

Xe > Kr > Ar > Ne > He

Q.261

XeF6 < XeF4 < XeF2

Q.262

Concentration solution of NH3 is water.

Q.263

Hydrogen bonding.

Q.264

Yellow flame.

Q.265

Yes NH3 + O2 → N2 + H2O

Q.266

Hydrogen bonding.

Q.267

Haber process.

Q.268

NH3 has hydrogen bonding like water.

Q.269

Good dielectric constant.

Q.270

NH3 has a tendency to form H-bond which helps to dissolve organic substances whereas its relatively low dielectric constant then water makes it a poor solvent for ionic inorganic substances.

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INORGANIC PAPER Q.271

CHEMISTRY

P. JOY

AgI has covalent bond so it is insoluble in water but it is soluble in NH3 due to complex formation. AgI + 2NH3 l [Ag(NH3)2]+

Q.272

NH4+ + NH2–

Q.273

Acid - base

Q.274

Reducing agent.

Q.275

N2 + H2O

Q.276

NH3 + HNO3

Q.277

N2O + H2O

Q.278

Linear

Q.279

One

Q.280

2p

Q.281

NO + NO2

Q.282

NO2

Q.283

NO2

Q.284

Diamagnetic

Q.285

N2O5

Q.286

Vapour

Q.287

50ºC → [Fe(CO) (NO) ] Fe(CO)5 + NO Pr 2 2 essure

Q.288

[Fe(H2O)5NO]SO4

Q.289

Phosphorous acid & phosphoric acids.

Q.290

+1 or +3 in phosphorous acid, +4 or +5 in phosphoric acid.

Q.291

Either one or two.

Q.292

Reducing agent

Q.293

White.

Q.294

One

Q.295

Orthophosphorous acid.

Q.296

NO

Q.297

Orthophosphoric acid.

Q.298

Pyrophosphoric acid.

Q.299

HPO3

Q.300

(HPO3)n

Q.301

HNO2, HNO3

Q.302

Oxidising, reducing, complex forming ability VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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Q.303

HNO3

Q.304

NO2 dissolved in concentrated HNO3

Q.305

aq. solution

Q.306

HNO3

Q.307

Birkeland Eyde & ostwald

Q.308

Nitrate ion.

Q.309

Urea.

Q.310

H4N2O4 & HNO4

Q.311

By direct oxidation of NH3 using Pt as a catalyst.

Q.312

P2O5

Q.313

HNO2 + HNO3

Q.314

NO2+

Q.315

P2O3, P2O5

Q.316

P2O5

Q.317

(i) P2O3 + 3H2O → 2H3PO2

P. JOY

(ii) 2P2O3 + 6H2O → 3H3PO3 + PH3 Q.318

P2O5

Q.319

P2O3

Q.320

P2O5

Q.321

(i) P2O5 + H2O → 2HPO3 (ii) P2O5 + 3H2O → 2H3PO4

Q.322

Chloramine NH2Cl [2NH3 + Cl2 → NH4Cl + NH2Cl]

Q.323

Hydrazine

Q.324

Ostwald Process.

Q.325

2N2(g) + 6H2O(g)

Q.326

NO

Q.327

O2, O3

Q.328

∆   → 3O (g) + 2KCl(s) (i) 2KClO3(s) MnO 2

Q.329

CO2 + SO2

Q.330

Sodium peroxide Na2O2

Q.331

Pale Blue

Q.332

F2O

Q.333

NO

Q.334

No vacant d-orbital.

2

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Q.335

Heating with a cobalt salt

Q.336

SO2

Q.337

BaO

Q.338

ZnO

Q.339

Elements that are on the borderline between metals and non-metals

Q.340

Sulphurous acid (HSO3)

Q.341

Alkaline

Q.342

Hydrogen

Q.343

High lattice energy

Q.344

BeO, SiO2, B2O3

Q.345

O2 2H2S + O 2 → 2H2O + 2S   → SO2

Q.346

8

Q.347

O2+ > O2 > O2– > O2–2

Q.348

O2

Q.349

Yes

Q.350

–1

Q.351

Na2O2 > MgO > ZnO > P2O5

Q.352

Small size, High EN, Absence of d orbitals.

Q.353

Priestley

Q.354

Strong covalent between two O atoms due to pπ-pπ overlapping.

Q.355

Non-linear

Q.356

O2 = paramagnetic, O3 = diamagnetic

Q.357

Nitrite ion

Q.358

By action of a silent electric discharge

Q.359

117º

Q.360

Increases to 3/2 times.

Q.361

O3

Q.362

(i) Oxidation of organic compound, (ii) Water purification

Q.363

Group 16

Q.364

Yes it can be oxidise all of them

Q.365

Zero

Q.366

10%

Q.367

P4 + O3 + H2O → H3PO4 Zero to + 5

Q.368

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Q.369

F2

Q.370

Red

Q.371

U.V. Rays

Q.372

Chlorofloro Carbon

Q.373

O3 + 2K+ + 2I– + H2O → KOH + I2 + O2

Q.374

Solid

Q.375

H2O2

Q.376

Skew, chain structure

Q.377

H2O or H2O2

Q.378

Its strong oxidizing nature ready decomposition

Q.379

Yes

Q.380

Reducing agent

Q.381

Acid

Q.382

Basic

Q.383

HO2 and OH

Q.384

BaSO4 + H2O

P. JOY

OH C 2H 5 Q.385

OH Q.386

No

Q.387

Peroxodisulfuric acid

Q.388

O2 > O3 > H2O

Q.389

8

Q.390

FeS2

Q.391

Frasch process

Q.392

γ-sulphur

Q.393

It is prepared by boiling milk of lime with sulphur and decomposing the product with HCl.

Q.394

369 K, transition temperature.

Q.395

Boil (i) 2S + Cl2   → S2Cl2 ∆ (ii) 3S + P4   → P4S3 1200 −1400K (iii) 2S + C   → CS2

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Q.396

(NH4)2 Sx

Q.397

SO2

Q.398

Trigonal planner, 120º

Q.399

SO2

Q.400

Reducing nature

Q.401

SO3

Q.402

+4 and +6

Q.403

FeS + H2SO4(dil.) → FeSO4 + H2S

P. JOY

H2(g) + S(l) → H2S(g) Q.404

Dibasic acid

Q.405

Bisulphides and hydrogen sulphides.

Q.406

It reacts with cations and produced coloured insoluble sulphides.

Q.407

s is pricipatted.

Q.408

H2S is readly oxidized into s or its disprotonation to SH– or S–2. It's ligand ability is very weak.

Q.409

Dilute chlorine.

Q.410

H2SO4, it is used in most of manufacturing process.

Q.411

Contact process, Lead chamber process.

Q.412

Fe(OH)3 remove As2O5 in contact process. They absorb As 2O5 on their surface.

Q.413

95%

Q.414

Contact process.

Q.415

Fe(OH)3

Q.416

SO3 + H2O → H2SO4 it is a violent reaction.

Q.417

2  → SO H2O S + O2 → SO2 VO H2SO4. 3  → 2 5

Q.418

Intermolecular hydrogen bonding.

Q.419

Bisulphate and sulphate.

Q.420

2

Q.421

+6

Q.422

H-bonding.

Q.423

Sparting of acid due to evolution of great amount of heat.

Q.424

H2SO4 is an oxidizing agent thus it can easily oxidised elements in their oxyacids.

Q.425

H2SO4 can form strong extensive H-bonds.

Q.426

Oxidising agent.

Q.427

Conc. H2SO 4 C6(H2O)6   → 6C + 6H2O

O

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Q.428

H2SO4

Q.429

H2SO3

Q.430

Zero and +4

Q.431

It can be reduce I2

Q.432

It dissolves unreacted AgBr from the photographic emulsion by complexation.

Q.433

Cl2 + H2O + Na2S2O3 → 2HCl + Na2SO4 + S

Q.434

Cl2 + H2O + Na2S2O3 → 2HCl + Na2SO4 + S Hypo is thus used as an antichlore.

Q.435

Na2S2O3

Q.436

Na2S + Na2S2O3 + I2 → 2NaI + Na2S2O3

Q.437

S4O6–2 (Tetrathionate)

Q.438

aq. solution of hydrogen halides.

Q.439

Strong affinity for hydrogen.

Q.440

(i) CaSO4 + 2HF(g), (ii) Na2SO2 + 2HCl(g)

Q.441

HF

Q.442

HI > HBr > HCl > HF

Q.443

High bond dissociation energy intermolecular hydrogen bonding.

Q.444

Due to high EN & small size of F.

Q.445

SbF5 is a strong e– pair acceptor.

Q.446

HF

Q.447

HF

Q.448

HF < HCl < HBr < HI

Q.449

HF forms a constant boiling mixture.

Q.450

It reacts with SiO2 of the glass.

Q.451

HF

Q.452

HCl

Q.453

HF

Q.454

HNO3

Q.455

HF > HCl > HBr > HI

Q.456

K+ and [HF2]–

Q.457

Fluorine

Q.458

ClOH > BrOH > IOH

Q.459

HClO < HClO2 < HClO3 < HClO4

Q.460

+1

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P. JOY

Q.461

Increases.

Q.462

Ba(ClO2)2 + H2SO4  → 2HClO2 + BaSO4

Q.463

Chlorites

Q.464

HClO4

Q.465

NaClO

Q.466

X = NH2Cl, chloramine

Q.467

Tetrahedral, sp3

Q.468

O− Cl → O

Q.469

HClO4

Q.470

HClO4 > HClO3 > HClO2 > HClO

Q.471

HClO4 > HClO3 > HClO2 > HClO

Q.472

HClO3 < HBrO3 < HIO3

Q.473

Cl2 + H2O → H+ + Cl– + HOCl

Q.474

+1 to +7

Q.475

Acidic

Q.476

Cl, Br, I

Q.477

Cl2O least and Cl2O7 most acidic.

Q.478

ClO2

Q.479

Ca+2, Cl–, OCl–

Q.480

CaOCl2 + H2O  → Ca(OH)2 + Cl2

Q.481

Ca(OH)2, Cl2

Q.482

It reacts with H2O and convert into Ca(OH)2 and Cl2 by auto oxidation.

Q.483

Ca(OH)2 + Cl2 → Ca(OCl) Cl + H2O

Q.484

Cl2

Q.485

The amount of Cl2 obtained from a sample of bleaching powder by treatment with excess of dilute acids or CO2.

Q.486

It produce nascent O by treatment with H2SO4.

Q.487

Autooxidation

Q.488

Mixed salt.

Q.489

35 to 38%

Q.490

Yes

Q.491

Halogen means salt forming.

Θ

.. ..

Autooxidation

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Q.492

At

Q.493

16th group elements

Q.494

Alkali metals and halogens

Q.495

Due to higher EN and their reactivity.

Q.496

I– and IO3–

Q.497



Q.498

Cl2

Q.499

Electrolysis of mixture of molten KF and HF

Q.500

Diaphragm is used to separate the two gases H2 and F2 otherwise these gases reacts explosively.

Q.501

By passing Cl2 gas into bromide salt solution

Q.502

6H+ + IO3– + I– → I2 + 3H2O

Q.503

6H+ + IO3– + I– → I2 + 3H2O

Q.504

When H2SO4 is added to NaCl with MnO2, Cl2 is evolved.

Q.505

K2MnF6 + SbF5 → K2SbF7 + MnF3 + ½F2

Q.506

True

Q.507

When halogen has – 1 oxidation state.

Q.508

He, Ne, Ar

Q.509

(a) Mg + Br2(l) → MgBr2 (b) P4 + Cl2(g) → PCl5 (c) S8 + F2(g) → SF6 (d) Xe(g) + F2(g) → XeF6

Q.510

Covalent nature

Q.511

UF6

Q.512

 → CaSO + HF (i) CaF2 + H2SO4 con.   ∆ 4  → Na SO + HCl (ii) NaCl + H2SO4 conc.   ∆ 2 4 Pt (as bijects) (iii) H2 + Br2   → HBr

5731 K

(iv) 2I2(s) + N2H4    → N2 + HI ∆

 → HI + S (v) I2 + H2S   ∆ Q.513

PCl5 + D2O → POCl3 + 2DCl

Q.514

Hypochlorite ion

Q.515

Cl2 + H2O + HgO → HOCl + HCl, HCl is absorbed by HgO

Q.516

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Q.517

Anode → Cl2 gas, Cathode → H2 and OH– obtain.

Q.518

Cl2 Ca(OH)2   → Ca(OCl)2. CaCl2.Ca(OH)2.2H2O

Q.519

2Cl2O + 2NaOH + H2O2 → 2NaClO2 + O2 + 2H2O

Q.520

Ba(ClO3)2 + H2SO4 → BaSO4 + 2HClO3

Q.521

Ba(ClO3)2 + Cl2 → Ba(ClO3)2

Q.522

THCl.

Q.523

Used in rockets as fuels.

Q.524

NaClO4 + NH4Cl → NH4ClO4 + NaCl

Q.525

x-x bond is stronger due to effective overlaping.

Q.526

Absence of unpaired electrons.

Q.527

Lower electronegativity difference.

Q.528

These are self ionizes

Q.529

Cl does not show +ve o.s. due to higher I.P.

Q.530

Fluorine

Q.531

I

Q.532

True

Q.533

True

Q.534

True

Q.535

True

Q.536

11

Q.537

IF7

Q.538

ICl is used as Wij's reagent in the estimated of the iodine number of fats and oils

Q.539

Iodine no. is a measure of the number of double bonds i.e. the degree of unsaturation of the fats.

Q.540

IF < IF3 < BrF < IF5 < BrF3 < ClF < IF2 < BrF5 < ClF3

Q.541

ICl3 is unstable.

Q.542

I+ → ICl, IBr, ICN, I+3 → ICl3, I(ClO4)3.IPO4.

Q.543

HOI (Hypo iodous acid) HCl.

Q.544

HF, HBrO3 bromic acid.

Q.545

(i) [I3]+ [AlCl4]– (ii) Cs+ [IF8]–

Q.546

ns2 np6

Q.547

Ne = 0, Ar = 0, Kr = 10, Xe = 10

Q.548

Gain or loss of electrons requires high energies.

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Q.549

Due to weak dispersion interactions between atoms.

Q.550

He

Q.551

He

Q.552

Rn

Q.553

~ 1%

Q.554

Ar

Q.555

Ne, Ar, Kr, Xe

Q.556

Natural gas

Q.557

He

Q.558

88

Q.559

1962

Q.560

Ionization enthalpies of O2 & Xe are close to each other.

Q.561

[XeF]+ [Pt2F11]–

Q.562

Electronegative

Q.563

Xe, O2

Q.564

Xenon, krypton

Q.565

Radon

Q.566

Ar, Ne, He

Q.567

KrF2

Q.568

6XeF4 + 12H2O → 4Xe + 2XeO3 + 24HF + 3O2

Q.569

XeF2, XeF4, XeF6

Q.570

XeO3– + 6HF

Q.571

XeOF4 & XeO2F2

Q.572

XeO3

Q.573

XeOF4

Q.574

XeO3 = Trigonal pyramidal, XeOF4 = Square pyramidal.

Q.575

XeO3 + OH– → HXeO4–

P. JOY

Ra226 → 86Rn222 + 2He4

hydrogen xenate ion Q.576

Perxenate ion XeO64–

Q.577

+8

Q.578

Yellow

Q.579

Oxidising

Q.580

(a) XeF4, (b) XeF2, (c) XeO3

Q.581

He non flammable & light gas

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P. JOY

Q.582

Neon

Q.583

He

Q.584

XeF2, XeF4, XeF6

Q.585

XeF4

Q.586

6

Q.587

XeF6

Q.588



Q.589

Pyramidal

Q.590

Tetrameric & hexameric

Q.591

Square pyramidal

Q.592

[XeF3]+ [SbF6]–

Q.593

4.2 K

Q.594

Helium

Q.595

Rn

Q.596

True

Q.597

(b)

Q.598

Li is better reducing agent. Because the big size of Na+ releases smaller heat of hydration.

Q.599

Na can reacts with air and water.

Q.600

Li is lighter than kerosense so it float over kerosene surface there if reacts with atmosphereic oxygen.

Q.601

The O2 of atmosphere tarnishes metallic surface by reacting with metal.

Q.602

(a, b)

Q.603

(a)

Q.604

(c)

Q.605

(a)

Q.606

Cs > Rb > K > Na > Li

Q.607

The hydration energy of Li is greater therefore a large amount of heat is evolved. Heat of hydration (Thermodynamic factor) is highest for Li but kinetic order of reactivity is Cs > Rb > K > Na > Li.

Q.608

Yes

Q.609

Solution become alkaline

Q.610

2M + ½O2 → M2O

Q.611

H2O, Na2O2, KO2, RbO2, CsO2

Q.612

(b)

Q.613

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Q.614

Elements which have (noble gas) ns1, ns2 configuration.

Q.615

Hydroxides and oxides of these metals are highly alkaline in nature.

Q.616

Na

Q.617

Alkali metals are highly reactive.

Q.618

Na2SO4.10H2O, Na2SO4, NaNO3

Q.619

d-block element

Q.620

s-block element

Q.621

Alkali metals forms metallic bond by valency e– s.

Q.622

This is due to lesser no. of electrons used by the elements to form electronic sea of metallic bond.

Q.623

This is due to covalent bond developed by the d-block elements in its metallic bond.

Q.624

Cs

Q.625

BCC

Q.626

Very low I.E.

Q.627

Alkali metal ion in aqueous state in alkali metal salts are colourless due all e's is paired state.

Q.628

Alkaly metals have inert gas configuration in ionic form.

Q.629

By flame test.

Q.630

Li – Crimson red Na – Yellow gold K – Green (pale) Rb – Blue Cs – Blue

Q.631

Because photons or light energy of invisible part of bunsen flame is absorb by e– s of alkali metal and get excited into higher energy shell. When electrons transite back it radiates light of visible region.

Q.632

Because energy gap of electron shells are different in different elements. Thus energy needed to transition and consecutive radiations are also different.

Q.633

To prepare volutile chlorides.

Q.634

Cu wire themselves in blue colour.

Q.635

Highly reliable

Q.636

Smaller ions forms oxide medium size ions form peroxide and larger ion forms superoxide.

Q.637

Antifluorite structure

Q.638

Depends upon the reactivity of metal toward oxygen.

Q.639

(a)

Q.640

It would have turned blue.

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IIT-JEE

CHEMISTRY

P. JOY

Na2O2 + H2O → 2NaOH + H2O2 Na2O + H2O → 2NaOH KO2 + H2O → 2KOH + H2O2 + O2

Q.642

O2

Q.643

(a) Na2O2 diamagnetic

(b) KO2 paramagnetic

(c) O2 paramagnetic

(d) Na2O paramagnetic

Q.644

Na2O2 + HCl(dil.)

Q.645

Li2O < Na2O < K2O < Rb2O < Cs2O

Q.646

They easily liberates oxygen.

Q.647

Na2CO3.10H2O, Na2CO3.7H2O, Na2CO3.H2O, Na2O

Q.648

s-block element.

Q.649

(d) Na2O2 and Na vapour are formed.

Q.650

s-block elements have calculate with high thermal stability due to less polarizing power of cations.

Q.651

Na2CO3 > NaHCO3 > H2CO3

Q.652

Cs2CO3 > ........... > Li2CO3

Q.653

(a) Li+ < Na+ < Rb+ < Cs+

(b) Li+ > Na+ > Rb+ > Cs+

(c) Li+ > Na+ > Rb+ > Cs+

(d) Li+ > Na+| > Rb+ > Cs+

(e) Li+ < Na+ < Rb+ < Cs + Q.654

4

Q.655

Cs > Rb > K > Na > Li

Q.656

When lithium is reacted with pure hydrogen lithium hydride is formed. Small size of lithium ion better balances hydride ion.

Q.657

Lithium charge to size ratio is very high as compared other alkali metal ion therefore this leads to covalent property in lithium compounds.

Q.658

NH4+, substituted ammonium ions, Ti+, Ag+, spherical + 1 complex (n5 – C5H5)2Co+

Q.659

Mg+2

Q.660

Na3N does not exist at room temperature N3– has high –ve charge & prefers covalent bonding which can only be developed by lithium ions among alkali metal ion.

Q.661

Due to small size of lithium ions the energy released by reaction of Li+ with water is greater than the energy needed to wides the crystal lattice.

Q.662

HClO4.3H2O

Q.663

(c)

Q.664

Li2CO3 is stable due to higher polarizing power of lithium.

Q.665

Hydration energy is greater then lattice energy.

Q.666

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Q.667

LiHCO3, NaHCO3, KHCO3, RbHCO3, NH4HCO3

Q.668

Na2CO3 is stable.

Q.669

Na2O2 + H2O → 2NaOH + H2O2

P. JOY

Na2O + H2O → 2NaOH Q.670

Li2CO3 decomposed into LiO and CO2 but Na2CO3 does not decomposed.

Q.671

Because all bicarbonates passes H+ as an essential cation which polarises CO3–2 ions and decomposes into CO2.

Q.672

All bicarbonates all soluble in water.

Q.673

Na2CO3 is more basic in aqueous state.

Q.674

Decomposed into 2Na2CO3 + 2H2O

Q.675

It forms a blue coloured solution of ammonated electrons and ammonated alkali metal ions.

Q.676

Blue colour turns to colour of metallic Cu.

Q.677

Due to ammonated e–s.

Q.678

Because blue colour is exihibited by ammonated electrons, and electrons obtained from all alkali metals are same.

Q.679

(c)

Q.680

Strong reducing agent.

Q.681

(All)

Q.682

Paramagnetic

Q.683

Fe By addition T.M. ion Na + NH3(l)   → NaNH2 + ½H2 ↑

Q.684

Residual deposition of alkali metal.

Q.685

(b)

Q.686

Due to pairing of electrons.

Q.687

(a, b, c, d)

Q.688

Fr

Q.689

223

Q.690

21 min.

Q.691

One

Q.692

Monovalent

Q.693

Paramagnetic

Q.694

Sodium peroxide

Q.695

Low solubility of LiF is due to its high lattice energy.

3+

Fr

Low solubility of CsI is due to smaller hydration energy. Q.696

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Q.697

Li

Q.698

Na < K < Rb < Li < Cs

Q.699

Cs < Rb < K < Na < K

Q.700

Li < Na < K < Rb < Cs

Q.701

Li < Na < K < Rb < Cs

Q.702

Cs < Rb < K < Na < Li

Q.703

Cs < Rb < K < Na < Li

Q.704

Li < Na < K < Rb < Cs

Q.705

Li > Na > K > Rb > Cs

Q.706

Li2CO3 < Na2CO3 < K2CO3 < Rb2CO3 < Cs2CO3

Q.707

CsHCO3 < RbHCO3, KHCO3 < NaHCO3 < LiHCO3

Q.708

MF < MCl < MBr < MI

Q.709

KI > KBr < KCl

Q.710

Li > K > Na

Q.711

Li2O, Na2O < K2O, Rb2O < Cs2O

Q.712

Li < Na < K < Rb < Cs

Q.713

BLi < Na < K < Rb < Cs

Q.714

BLi < Na < K < Rb < Cs

Q.715

MgSO4.7H2O

Q.716

Due to the formation of a surface film of the oxide.

Q.717

H2

Q.718

MgO, Mg3N2

Q.719

Grignard Reagent

Q.720

Reducing agent.

Q.721

Mg

Q.722

Reaction is reversible & proceeds efficiently when CO2 is escaped which is only above 1100 K. CaCO3 l CaO + O2

Q.723

Quick time

Q.724

Disintegration of lump of lime in limited amt. of water.

Q.725

Sodalime.

Q.726

(a) CaO + SiO2 → CaSiO3 (b) CaO + P4O10 → Ca(PO4)2

Q.727

Ca(OH)2 when water is added to slaked lime.

Q.728

Aq. solution of Ca(OH)2 VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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Q.729

Milk of lime.

Q.730

It turns milky.

Q.731

Ca(HCO3)2

Q.732

Ca(ClO)2

Q.733

CaSO4.2H2O

Q.734

When gypsum CaSO4.2H2O is heated to 393 K.

Q.735

Due to increased nuclear charge & smaller size.

Q.736

Covalent

Q.737

(i) Mg(OH)2 < Ca(OH)2 < Sr(OH)2 < Ba(OH)2

P. JOY

(ii) Mg(OH)2 < Ca(OH)2 < Sr(OH)2 < Ba(OH)2 (iii) Mg(OH)2 < Ca(OH)2 < Sr(OH)2 < Ba(OH)2 Q.738

Beryllate ion.

Q.739

Four

Q.740

MgBr2 & MgI2

Q.741

Ca

Q.742

CaF2

Q.743

(i) BeCO3 < MgCO3 < CaCO3 < SrCO3 < BaCO3 (increasing thermal stability) (ii) CaSO4 > SrSO4 > BaSO4 (Increasing solubility) (iii) Ca(C2O4)2 > Sr(C2O4)2 > Ba(C2O4)2 (increasing solubility)

Q.744

Ba

Q.745

∆ 2Ca(NO3)2    → 2CaO + 4NO2 + O2

Q.746

Strontium nitrate.

Q.747

Greater hydration energies of Be2+ & Mg2+ ions overcome the lattice energy factor.

Q.748

Be have no vacant d-orbital while other have it.

Q.749

MgSO4.2H2O, MgSO4.7H2O

Q.750

By treating with H2SO4

Q.751

By fractional crystallization

Q.752

MgSO4.7H2O

Q.753

[Mg(H2O)6]SO4.H2O

Q.754

Potash magnesis is a Fertilizer & Its chemical composition K2SO4.MgSO4.6H2O.

Q.755

Purgative in medicine.

Q.756

Ca2SiO4, Ca3SiO5, Ca3Al2O6

Q.757

When it is mixed with water & send the powder herdered into a block that resembled the natural limestone quairried in the Isle of portland.

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P. JOY

Q.758

J. Aspdin in 1824.

Q.759

It is the hydration of the molecules of the constituents and their rearrangement.

Q.760

Be

Q.761

2

Q.762

7th

Q.763

Alkaline earth metals due to increased nuclear charge.

Q.764

After first ionization alkali metals aquired inert gas configuration therefore their second I.P. is very higher.

Q.765

Be, Mg : electron are too strongly bound to get excited by flame.

Q.766

Ba

Q.767

K3[Cu(CN)4]

Q.768

All

Q.769

I > Br > Cl > F

Q.770

+3

Q.771

Cast iron

Q.772

3d10 4s0 configuration

Q.773

Zero

Q.774

Mixture of Cu + Sn + Zn

Q.775

Cu+2 and pb+2

Q.776

H2S

Q.777

MnO2

Q.778

Transition of electrons between d-orbitals of a metal.

Q.779

Ag+ polarises Br– and I–

Q.780

Small and highly charged ions and have vacant orbitals to accept lone pair of electrons from ligand.

Q.781

A deep blue voilet coloured compound CrO(O2)2 is formed.

Q.782

Mn

Q.783

Cr(OH)2 < Cr(OH)3 < CrO2(OH)2 acid strength increases with increase in oxidation number.

Q.784

Cr(OH)3 + 3HCl → CrCl3 + 3H2O base Cr(OH)3 + NaOH → Na[Cr(OH)4] acid

Q.785

Because of formation of oxide layer.

Q.786

[Fe(CN)6]3– has one unpaired electron (d2sp3 hybridised Fe3+) while [Fe(H2O)6]3+ has five unpaired electrons (sp3d2 hybridised Fe3+) VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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INORGANIC PAPER Q.787

(a) 36

Q.788

I(b), II(a), III(c)

Q.789

[Co(H2O)4Cl2]Cl.H2O

Q.790

[Ni(H2O)4]2+ > [Fe(CN)6]2– > [Fe(CN)6]4– = [Ni(H2O)4]2+

Q.791

N(N + 2) =

P. JOY

CHEMISTRY

(b) 33

(c) 36

(d) 36

3+ 35 ⇒ N = 5 (unpaired electrons) ⇒ x = 3(Fe )

Fe3+ = [Ar] 3d5 Q.792

The s- and p-block elements do not have a partially filled d-shell so there cannot be any d-d* transition. The energy to promote as s- or p-electron to a higher energy level is much greater and corresponds to ultraviolet light being absorbed. Thus compound will not be coloured.

Q.793

Hg2+ has all filled 5d orbitals (no unpaired electron is 5d), hence no d-d* transition, hence colourless.

Q.794

Sc(21) : [Ar] 3d! 4s2 Sc3+ : [Ar] 3d0 no unpaired electron in d-orbital, hence no (d-d*) transition hence colourless. Ti(22) : [Ar] 3d2 4s2 Ti3+ : [Ar] 3d1 due to unpaired electron in d-orbital (d-d*) transition possible hence coloured.

Q.795

There is a steady decrease in the radii as the atomic number of the lanthanide element increases. It is because, for every additional proton in a nucleus, the corresponding electron goes into 4f shell which is too diffused to screen the nucleus as effectively as more localised inner shell. Hence the attraction of the nucleus for the outermost electrons increases steadily with the atomic number of the lanthanides. This contraction in size is quite regular. This is called Lanthanide Contraction.

Q.796

Lattice energies, solvation energies and ionisation energies would be similar.

Q.797

cis-2-butene

Q.798

Natta

Q.799

Zeolite

Q.800

5VO2+ + MnO4– + H2O → 5VO2+ + Mn2+ + 2H+

Q.801

CrO3

Q.802

VI

Q.803

VI (O = – 2 diperoxo = – 4)

Q.804

VI

Q.805

V

Q.806

Cr2O72– < Cr3+ < Cr2+ Smaller the oxidation state of the element in the ion, greater the reducing nature.

Q.807

2MnO4– + 5H2O2 + 6H+ → 2Mn2+ + 5O2 + 8H2O 2MnO4– + 3H2O2 → 2MnO2 + 3O2 + 2OH– + 2H2O

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IIT-JEE

INORGANIC PAPER Q.808

CHEMISTRY

P. JOY

Aqueous CO2 releases H+ which can convert MnO42– into MnO2 and MnO4– in a disproportionation reaction. CO2 + H2O l H+ + HCO3– 3MnO42– + 4H+ → MnO2 + 2MnO4– + H2O

Q.809

AgBr + 2Na2S2O3 → Na3[Ag(S2O3)2] + NaBr

Q.810

In both cases Fe2+ ions are formed due to reduction. Hence solution appears light green.

Q.811

Fe2+ gives green ppt with NaOH and Fe 3+ gives red brown ppt.

Q.812

2K2HgI4 + NH3 + 3NaOH →

Hg O Hg

NH 2

I + 4KI + 3NaI + 2H2O

(Iodide of M illo n’s ba se) b row n p pt

Q.813

70% Cu + 30% Zn

Q.814

75% Cu + 25% Ni

Q.815

60% Ni + 20Fe + 20% Fe

Q.816

NO3–, HCO3–, CH3COO–

Q.817

NO3–

Q.818

Na2CO3

Q.819

CO32–

Q.820

CO2

Q.821

S2– → SO2 and CO32– → CO2

Q.822

CaCO3

Q.823

Ca(OH)2

Q.824

Ca(HCO3)2

Q.825

SO2

Q.826

Green.

Q.827

Cr+3

Q.828

Basic.

Q.829

Dichromate or chromate.

Q.830

Oxidising agents Cl2, Br2, KIO3, Cu4+, K2Cr2O7, KMnO4.

Q.831

Reducing agents.

Q.832

ppt dissolves through formation of CO2

Q.833

CO3– and SO3–

Q.834

In presence of I– and Br–

Q.835

Pb, Ag, Sb, Sn VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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P. JOY

Q.836

NO3–, NO2–, chlorates.

Q.837

Cl2 is evolved as Cr2O72– are oxidising agent and oxidises Cl– into Cl2

Q.838

HCl

Q.839

Cr2F2, violet

Q.840

HCl

Q.841

Cl2

Q.842

Cl2

Q.843

CrO42– (yellow colored ion) is formed.

Q.844

White ppt of AgCl

Q.845

NH3 solution, SO32– solution, cyanide solution, hypo solution, amine solution.

Q.846

AgI

Q.847

Fazan's theory.

Q.848

AgCl

Q.849

Cl–

Q.850

Soluble in hot water.

Q.851

H3PO4–

Q.852

CCl4, CS2

Q.853

Br– → Br2 (Red) I– → I2 (violet / purple)

Q.854

Cl2 water, HOCl, NaOCl, conc. HNO3

Q.855

Redox reaction take place and Br2 is liberated.

Q.856

H2SO4, HNO3, MnO2, PbO2, Cl2 water, KMnO2, NaOCl, HOCl

Q.857

Cl2 and F2

Q.858

SO2 and I2 vapour is released.

Q.859

HCl, HBr and HI

Q.860

H2S

Q.861

All can be oxidised.

Q.862

Formation of white ppt of Cu2I2

Q.863

I2 is formed

Q.864

K2HgI4

Q.865

HgI2 → K2HgI4

Q.866



Q.867

It forms free iodine, which is detected by starch.

Q.868

NO VISION KOTA, 608-A, TALWANDI KOTA (RAJ.) Ph. 0744 - 6450883, 2405510

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Q.869

NO

Q.870

+1

Q.871

Al, Zn

Q.872

NO2–, NO3–

Q.873

NO2

Q.874

HNO2 i.e. formed releasing NO.

Q.875

Pale, Blue

Q.876

NO2

Q.877

Ba3(PO4)2

Q.878

Sulphide

Q.879

PbSO4, BaSO4, Ag2SO4, HgSO4.HgO

Q.880

HgSO4.HgO

Q.881

(NH4)2MO4

Q.882

(NH4)6Mg7O24.4H2O

Q.883

(NH4)3 [P(MO3O10)4]

Q.884

Canery yellow

Q.885

Yellow ppt of ferric phosphate is formed.

Q.886

White gelatinous ppt of zirconyl phosphate is formed.

Q.887

Phosphate and arsenate

Q.888

CO, CO2, H2O vapours

Q.889

Blue

Q.890

Redox takes place.

Q.891

Orange → Green

Q.892

CH3COO–

Q.893

Smell of vinegar is evolved.

Q.894

Silver acetate

Q.895

CH3COO–

Q.896

FeCl3

Q.897

{Fe3(OH)2(CH3COO)6}+

Q.898

Fe(OH)2 (CH3COOH)

Q.899

Formate

Q.900

(C2O42–)

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