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Why does acetyl chloride react with water much more rapidly than heptanoyl chloride or benzoyl chloride?

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Why does acetyl chloride react with water much more rapidly than heptanoyl chloride or benzoyl chloride?

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When you add water to these compounds it will act as a nucleophile and displace the Cl, leaving you with the carboxylic acid, however it will react much more readily with acetyl chloride rather than the other two because in acetyl chloride the site of attack is much less hindered.

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