Ochem Question

This forum made possible through the generous support of SDN members, donors, and sponsors. Thank you.
Don't quote me on this but I think it's just a matter of convenience. The substitution reaction is reversible, so to increase amide yield, you use an excess of ammonia to drive the reaction forward. With an acyl halide, you get a HX byproduct, which can react with some excess ammonia in solution to form NH4X for a total of two ammonias consumed in reaction. With an anhydride, the initial reaction froms an amide and a carboxylic acid. The carboxylic acid can then react with another molecule of ammonia to from an ammonium alkanoate, again for a total of two ammonias consumed. In both cases, the second ammonia is used in a subsequent reaction with the byproducts of amide formation.
 
Yep, just acts as a proton sponge, which eliminates the strongly acidic conditions that make Amide hydrolysis occur
 
One act as nucleophile to replace Cl or RCOO, other act as base to react with HCl or RCOOH to produce salt.
 
Last edited:
Top