why does p-methoxybenzyl bromide reacts with
Why does p-methoxybenzyl bromide reacts with ethanol faster than p-nitrobenzylbromide Solution) Because o-ch3 is electron donating group while NO2 is a electron withdrawing group
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e1cb means elimination unimolecular of the conjugate base this type elimination proceeds through the carbanion mechanisman carbon compound acting as
why does p-methoxybenzyl bromide reacts with ethanol faster than p-nitrobenzylbromide solution because o-ch3 is electron donating group while no2 is
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