Question about base catalyzed transesterification mechanism & isomerization.
Say I have a compound with two carboxylic groups on it, and both are esters, but with different alcohols. Would a base catalyzed transesterification
(to isomerize) cause the alcohol groups present at each ester to swap around and become jumbled? Or does the transesterification only work if there
are free-nucleophiles in the solution to attack?
I read that for the transesterification to happen, an akloxide needs to form between the base and free alcohol first? I guess my question is can
another deprotonated ester behave in this similar manner and effect transesterification?
[Edited on 13-8-2015 by RareEarth]
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