Question:
\( p \)-cresol reacts with chloroform in alkaline medium to give the compound A which adds hydrogen cyanide to form the compound B. The latter on acidic hydrolysis gives chiral carboxylic acid. The structure of the carboxylic acid is:
\( p \)-cresol reacts with chloroform in alkaline medium to give the compound A which adds hydrogen cyanide to form the compound B. The latter on acidic hydrolysis gives chiral carboxylic acid. The structure of the carboxylic acid is:
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The reaction of phenols with chloroform in alkaline conditions followed by hydrolysis leads to the formation of chiral carboxylic acids.
Updated On: Jan 12, 2026
- A
- B
- C
- D
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The Correct Option is A
Solution and Explanation
Step 1: \( p \)-cresol reacts with chloroform in alkaline medium to form a cyano compound.
Step 2: The final product after hydrolysis gives a chiral carboxylic acid. The structure of the carboxylic acid is \( \text{CH}_3\text{C}(\text{OH})\text{COOH} \).
Final Answer: \[ \boxed{\text{CH}_3\text{C}(\text{OH})\text{COOH}} \]
Step 2: The final product after hydrolysis gives a chiral carboxylic acid. The structure of the carboxylic acid is \( \text{CH}_3\text{C}(\text{OH})\text{COOH} \).
Final Answer: \[ \boxed{\text{CH}_3\text{C}(\text{OH})\text{COOH}} \]
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