Question:medium

Identify 'B' in the following reaction
Ethyl cyanide \(\overset{\text{H}_2\text{O}\,}{\rightarrow }\text{A}\overset{\text{H}_2\text{O / dil HCl}\,}{\rightarrow }\text{B}+\text{NH}_3\)

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Nitrile partly hydrolyses to an amide (A). Further hydrolysis gives the acid (B) and ammonia.
Updated On: Oct 1, 2026
  • Ethanoic acid
  • Ethanamide
  • Propanoic acid
  • Propanamide
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The Correct Option is C

Solution and Explanation

Step 1: Track the carbons:
Ethyl cyanide has $\text{C}_2\text{H}_5$ plus the nitrile carbon, three carbons in all. So B must be a three-carbon compound, ruling out ethanoic acid and ethanamide.

Step 2: Track the stages:
First stage adds one water to give the amide A: propanamide. The question says the second stage gives B plus $\text{NH}_3$. An amide loses ammonia only when it is hydrolysed to the acid.

Step 3: Conclusion:
So B is $\text{CH}_3\text{CH}_2\text{COOH}$, propanoic acid. Propanamide is A, not B.

Final Answer:
Option (C). \[ \boxed{\text{Propanoic acid (C)}} \]
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