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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p-cresol reacts with chloroform in alkaline medium to form a compound that undergoes acidic hydrolysis to give a chiral carboxylic acid.
Updated On: Jan 12, 2026
- A
- B
- C
- D
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The Correct Option is A
Solution and Explanation
Step 1: Analyze the reaction steps.
The reaction involves chloroform and p-cresol to form a product that undergoes further reactions, leading to a chiral carboxylic acid.
Step 2: Conclusion.
Thus, the carboxylic acid has the structure \( \text{CH}_3 \text{C} (\text{OH}) \text{COOH} \).
Final Answer: \[ \boxed{\text{CH}_3 \text{C} (\text{OH}) \text{COOH}} \]
The reaction involves chloroform and p-cresol to form a product that undergoes further reactions, leading to a chiral carboxylic acid.
Step 2: Conclusion.
Thus, the carboxylic acid has the structure \( \text{CH}_3 \text{C} (\text{OH}) \text{COOH} \).
Final Answer: \[ \boxed{\text{CH}_3 \text{C} (\text{OH}) \text{COOH}} \]
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