double bond.* General formula CnH2n* Hydrocarbon with carbon-carbon triple bond. General formula CnH2n-2 Both are unsaturated hydrocarbon because they contain less hydrogen per carbon.
Nomenclature Choose longest chain with C=C as parental chain with -ene- suffix.* Number the carbon atom beginning with the end nearest to the C=C. Side chain act as prefix and parental chain as suffix. Side chain named alphabetically and position on parental chain indicated. In naming parental alkene, position of C=C indicated by smaller number of attachment point. Alkyne naming is similar except C C as parental chain with -yne- suffix.
INDICATOR * Express Alkenes Express Alkynes Express Both Alkenes Alkynes
Cracking
[CH2-CH2] n Steam Dehydrogenation800°C process
[CH2=CH2] n + H2
ALKENES PREPERATION Dehydrohalogenation Dehydration of Alcohol
CnH2n+1OH [CH2=CH2] n + H2O Alcohol vapour is passed through hot alumina @ heated with excess sulphuric acid
Hydrohalogenation
[CH2=CH2] n +HX
CnH2n+1X
If according to Markonikoff produce major product If according to anti Markonikoff produce minor product
CnH2n+1X -HX
[CH2=CH2] n + H2
KOH (in alcohol)
Haloalkane boiled in potassium hydroxide dissolved in alcohol
Halogenation
[CH2=CH2] n + X
n [CH2-CH2] X2
via electrophilic addition
Hydration
[CH2=CH2] n +H2O
CnH2n+1OH
Catalyst phosphoric acid at 300°C
Hydrogenation
[CH2=CH2] n +H2
n [CH2-CH2]
ALKENES REACTIONS Oxidation
[CH2=CH2] n
n [CH2-CH2] (OH)2
Reaction in Bromine Water
Test for alkene unsaturation Br2
[CH2=CH2] nH2O Addition of Sulphuric Acid
[CH2=CH2] n +H2SO4
n [CH2-CH2] OHBr
Via electrophilic addition
n [CH2-CH2] H2SO4 (alkyl hydrogen sulphate) Polymerisation
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