When methyl benzoate bears a substituent at the para position, the rate of hydrolysis of the ester
Question:
When methyl benzoate bears a substituent at the para position, the rate of hydrolysis of the ester moiety depends on the nature of the substituent at the para position. Apparently, a methoxy substituent renders the ester less reactive, while a nitro substituent renders the ester more reactive. Explain this observation.
Fantastic news! We've Found the answer you've been seeking!
Step by Step Answer:
Related Book For
Question Posted: