In the alkaline hydrolysis of ethyl acetate

CHEMISTRY · Single correct · A Level · Chemistry · Introduction to organic chemistry · Introduction to organic chemistry

Problem

In the alkaline hydrolysis of ethyl acetate, OH−\text{OH}^- attacks the carbonyl carbon to form a tetrahedral intermediate bonded to the hydroxide oxygen; the intermediate then collapses, regenerating OH−\text{OH}^-. Into which major category of catalysis does the role of OH−\text{OH}^- in this mechanism fall? (a) Binding (orientation) catalysis (b) General base (acid–base) catalysis without covalent intermediate (c) Covalent catalysis involving nucleophilic attack by OH−\text{OH}^- (d) Surface (heterogeneous) catalysis

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