Hydrolysis of ester bonds typically yields which pair?

Study for the CIE Chemistry Advanced Subsidiary (AS) Level Test. Prepare with multiple-choice questions and detailed explanations. Master the exam!

Multiple Choice

Hydrolysis of ester bonds typically yields which pair?

Explanation:
Ester hydrolysis adds water to the ester and breaks the C–O bond, separating the molecule into two parts: the acyl (carbonyl) portion becomes a carboxylic acid (or carboxylate salt under basic conditions), and the other alkyl part becomes an alcohol. That means the typical products are an alcohol and a carboxylic acid (or its salt), not an aldehyde, ether, ketone, or anything else. Under acidic conditions the carboxyl product is the free acid; under basic conditions you’d get the carboxylate salt, but the alcohol and the carboxylate pair is still the outcome.

Ester hydrolysis adds water to the ester and breaks the C–O bond, separating the molecule into two parts: the acyl (carbonyl) portion becomes a carboxylic acid (or carboxylate salt under basic conditions), and the other alkyl part becomes an alcohol. That means the typical products are an alcohol and a carboxylic acid (or its salt), not an aldehyde, ether, ketone, or anything else. Under acidic conditions the carboxyl product is the free acid; under basic conditions you’d get the carboxylate salt, but the alcohol and the carboxylate pair is still the outcome.

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