Chemistry > Alcohols, Phenols and Ethers > 4.0 Preparation of Alcohol
Alcohols, Phenols and Ethers
1.0 Alcohols
2.0 Classification of alcohols
3.0 Physical properties of the alcohol
3.0 Physical properties of the alcohols
4.0 Preparation of Alcohol
4.1 By hydrolysis of alkyl halide
4.2 Acid catalysed hydration of alkenes
4.3 Oxymercuration Demercuration
4.4 Hydroboration-oxidation
4.5 Hydroxylation of alkenes
4.6 From organometallic compounds
4.6 Reduction of Esters
5.0 Grignard reagent
5.1 Reaction & Mechanism
5.2 Product of Grignard reagent
5.3 Planning a Grignard synthesis
5.4 Restriction of the use of Grignard reagents
6.0 Chemical properties of alcohols
6.1 Acidic character
6.2 Dehydration
6.3 Reaction with phosphorus trihalide or thionyl chloride
6.4. Reaction with hydrogen halide
6.5 Oxidation of Alchols
7.0 Tests for Alchols
8.0 Ethers
9.0 Chemical Properties of Ethers
10.0 Aryl Ethers
11.0 Epoxides
12.0 Phenols
13.0 Preparation of Phenol
14.0 Physical Properties of Phenol
15.0 Chemical properties of phenols
4.2 Acid catalysed hydration of alkenes
4.2 Acid catalysed hydration of alkenes
4.3 Oxymercuration Demercuration
4.4 Hydroboration-oxidation
4.5 Hydroxylation of alkenes
4.6 From organometallic compounds
4.6 Reduction of Esters
5.2 Product of Grignard reagent
5.3 Planning a Grignard synthesis
5.4 Restriction of the use of Grignard reagents
6.2 Dehydration
6.3 Reaction with phosphorus trihalide or thionyl chloride
6.4. Reaction with hydrogen halide
6.5 Oxidation of Alchols
Alkenes add water in the presence of an acid catalyst to yield alcohol. The addition takes place according to Markovnikov regioselectivity. The reaction is reversible and the mechanism for the acid-catalyzed hydration of an alkene is simply the reverse of that for the dehydration of an alcohol.
Acid-catalyzed hydration of alkene has limited synthetic utility. However, because of carbocation intermediate rearrangement may take place. Thus a mixture of isomeric alcohols may result.
