CH4 is more stable than SiH4
1 answer:
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Answer:
A) Ethanoic acid and ammonium chloride.
Explanation:
Amides go through acid hydrolysis to produce carboxylic acid and ammonia by heating in aqueous acid. The acid hydrolysis reaction is produced through the <u>nucleophilic addition of water to the protonated amide</u>, then comes the transference of a proton from the oxygen to the nitrogen to make nitrogen a better leaving group, and finally, the subsequent elimination (see attachment).
In this case, the products formed with the reaction of ethanamide and aqueous HCl will be <u>ethanoic acid and ammonium chloride</u>.
