Amides hydrolyze in acidic media, under heating, forming amines and carboxylic acids.

acid-hydrolysis

Ethanamide [1] hydrolyzes in a sulfuric medium to form ethanoic acid [2].
The reaction mechanism occurs in the following steps:

Stage 1. Protonation of carbonyl oxygen.

acid-hydrolysis

Stage 2. Nucleophilic attack of water on carbonyl carbon

acid-hydrolysis

Stage 3. Deprotonation of water and protonation of the amino group.

acid-hydrolysis

Stage 4. ammonia removal

acid-hydrolysis

Stage 5. deprotonation of carbonyl oxygen

acid-hydrolysis