What happens when an ester undergoes hydrolysis under acidic conditions?

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Multiple Choice

What happens when an ester undergoes hydrolysis under acidic conditions?

Explanation:
Under acidic hydrolysis, an ester reacts with water in the presence of an acid to give a carboxylic acid and an alcohol. The acid protonates the carbonyl oxygen, making the carbonyl carbon more electrophilic so water can attack. Water adds to form a tetrahedral intermediate, then the alkoxy group is protonated and leaves as alcohol. After deprotonation, the carbonyl re-forms to give the carboxylic acid, with the acid catalyst regenerated. This is different from basic hydrolysis, which yields a carboxylate salt instead of the neutral acid. The other options don’t fit because they omit the carboxyl product, propose a ketone, or imply salt formation under acidic conditions.

Under acidic hydrolysis, an ester reacts with water in the presence of an acid to give a carboxylic acid and an alcohol. The acid protonates the carbonyl oxygen, making the carbonyl carbon more electrophilic so water can attack. Water adds to form a tetrahedral intermediate, then the alkoxy group is protonated and leaves as alcohol. After deprotonation, the carbonyl re-forms to give the carboxylic acid, with the acid catalyst regenerated. This is different from basic hydrolysis, which yields a carboxylate salt instead of the neutral acid. The other options don’t fit because they omit the carboxyl product, propose a ketone, or imply salt formation under acidic conditions.

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