Conversion of propene to 1-bromopropane
This is anti-markovnikov addition reaction.
CH3−CH=CH2PropeneHBr/peroxide−−−−−−−−→CH3−CH2−CH2−Br1−Bromopropane
Conversion of 1-bromopropane to propan-1-ol
This is nucleophilic substitution reaction.
CH3−CH2−CH2−Br1−Bromopropanesq.KOH/Δ−−−−−−−→CH3−CH2−CH2−OHPropan−1−ol
Conversion of ethanol to ethyl chloride
Conversion of ethyl chloride to sodium acetylide
Reaction of sodium acetylide and ethyl chloride
Conversion of 1-bromopropane to propene
Conversion of propene to 2-bromopropane
Conversion of toluene to benzyl chloride
Conversion of benzyl chloride to benzyl alcohol
Conversion of benzene to bromobenzene
Conversion of bromobenzene to 4-bromonitrobenzene
Conversion of benzyl alcohol to benzyl chloride
Conversion of benzyl chloride to benzyl cyanide
Conversion of benzyl cyanide to 2-phenylethanoic acid
Conversion of ethanol to bromoethane
Conversion of bromoethane to propanenitrile
Conversion of aniline to benzene diazonium chloride
Conversion of benzene diazonium chloride to chlorobenzene
Conversion of 2-chlorobutane to 3,4-dimethylhexane
Conversion of 2-methyl-1-propene to 2-chloro-2-methylpropane
It occurs via Markovnikov’s addition of
HCl on double bond.
Conversion of ethyl chloride to propanenitrile
It occurs via nucleophilic substitution reaction
Conversion of propanenitrile to propanoic acid
It is a hydrolysis reaction which changes nitrile functional group to carboxylic acid.
Conversion of but-1-ene to 1-bromobutane
It occurs via anti-markovnikov’s addition of
HBr on double bond in presence of peroxide
(ROOR).
Conversion of 1-bromobutane to n-butyl iodide
This is a Finkelstein reaction which involves halogen exchange.
Conversion of 2-chloropropane to propene
It is a elimination reaction which led to formation of alkene from halide in presence of strong base and heat.
Conversion of propene to 1-bromopropane
It occurs via anti-markovnikov’s addition of
HBr on double bond in presence of peroxide
(ROOR).
Conversion of 1-bromopropane to 1-propanol
It occurs via nucleophilic substitution of bromide by hydroxide.
Conversion of isopropyl alcohol to iodoform
This is called as Iodoform reaction which led to formation of Iodoform
(CHI3) as one of the product.
Conversion of chlorobenzene to p-chloronitrobenzene
It is a electrophilic substitution reaction for nitro group and named as nitration.
Conversion of p-chloronitrobenzene to p-nitrophenol
It occurs via nucleophilic substitution on aryl halide.
Conversion of 2-bromopropane to propene
It is a elimination reaction which led to formation of alkene from halide in presence of strong base and heat.
Conversion of propene to 1-bromopropane
It occurs via anti-markovnikov’s addition of
HBr on double bond in presence of peroxide
(ROOR).
Conversion of chloroethane to butane
It is called as wurtz reaction, where product contains double the number of carbons present in halide.
Conversion of benzene to chlorobenzene
It is a electrophilic substitution reaction for Halogen group and named as halogenation.
Conversion of chlorobenzene to diphenyl
It is called as fittig reaction, which involves joining of
2 aryl groups in presence of sodium in dry ether.
Conversion of tert-Butyl bromide to 2-Methylpropene
It is an elimination reaction which led to formation of alkene from halide in presence of strong base and heat.
Conversion of 2-Methyl propene to isobutyl bromide
It occurs via anti-markovnikov’s addition of
HBr on double bond in presence of peroxide
(ROOR).
Conversion of aniline to phenyl isocyanide
This is called as carbylamine reaction, which Involves preparation of foul smelling isocyanide compound from aniline, chloroform and base mixture In presence of heat.