Reaction of Alcohols With Acyl Chlorides
- Acyl chlorides are reactive organic compounds with a -COCl functional group
- The carbonyl carbon is electron-deficient and has a partial positive charge
- It is therefore susceptible to nucleophilic attack
- The carbon-chlorine bond breaks and white fumes of hydrogen chloride, HCl, are formed
Reaction with alcohols and phenols
- Acyl chlorides react with alcohols and phenols to form esters in a nucleophilic substitution reaction
- The -OH group acts as a nucleophile and attacks the carbonyl carbon to substitute the chlorine atom
- Forming esters from acyl chlorides rather than carboxylic acids is more effective because::
- Acyl chlorides are more reactive (so they produce the ester faster)
- Acyl chloride reactions go to completion (so more of the ester is produced)
Reaction with alcohols
- The reaction of acyl chlorides with alcohols is vigorous and white fumes of HCl gas are formed
Esterification of an aliphatic alcohol using an acyl chloride 
Acyl chlorides react vigorously with alcohols to form esters
Reaction with phenols
- For the reaction of acyl chlorides with phenols to occur, heat and a base are required
- The base is needed to deprotonate the phenol and form a phenoxide ion
- The phenoxide ion is a better nucleophile than the original phenol molecule and will be able to attack the carbonyl carbon
Esterification of phenol using an acyl chloride
Acyl chlorides react with phenols when heated and in the presence of a base to form esters
A base is needed to form a phenoxide ion which is a better nucleophile than phenol; now, nucleophilic attack on the carbonyl carbon can more readily occur
