Why are the OH groups of carboxylic acids more acidic than alcohols?

Question

Quizplus · Accepted Answer

The resonance stabilization of the carboxylate ion contributes to the acidity of carboxylic acids. The delocalization of negative charge in the carboxylate ion is possible due to resonance with the carbonyl group, which stabilizes the negative charge and makes it easier for a proton to dissociate from the OH group. This resonance stabilization is not present in alcohols, making the OH group of carboxylic acids more acidic than that of alcohols.

Why Are the OH Groups of Carboxylic Acids More Acidic