Why are acid chlorides more reactive towards nucleophilic

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Reference no: EM13131851

Why are acid chlorides more reactive towards nucleophilic substitution than ethyl esters?

Give an explanation of why acid chlorides are more reactive toward nucleophilic substition than are the corresponding ethyl esters. (When considering the nature of the leaving group and the rate-determining step in an addition-elimination sequence).

Reference no: EM13131851

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