Inactive Tutor answered 02/08/16
Tutor
New to Wyzant
Hi Sam
Treating phenyl amine with ethanoyl chloride (an acyl chloride) proceeds via a nucleophilic acyl substitution reaction and the resulting product as an amide, a carboxylic acid derivative. Acylation of the amino group is a useful synthetic strategy for electrophilic substitution reactions as the resulting amide group is a moderate activator (the amino group is a strong activator).
Hope this answers your question.