If given this balanced equation: #2C_7H_6O + C_3H_6O -> C_17H_14O +2H_2O# Why is the acetone deprotonated and not the benzaldehyde?

1 Answer
P dilip_k
May 27, 2016

As explained below

Explanation:

google image
The reaction occurs according to the mechanism as shown above via the formation of carboanion (#CH_3COCH_2^-#) due to removal of proton from acetone molecule by #OH^-# ion. This ion exists as following resonance structures as enolate ion and gets stabilized thus facilitating its formation in the course of reaction. ( The resonance structures are shown below)

The deprotonation of acetone is thus favored because this stabilization of deprotonated ion from bezaldehyde is not possible.

google image
The resonance structures of the anion obtained by deprotonation of acetone

Related questions
See all questions in Quick Introduction of Structures
Impact of this question
2830 views around the world
You can reuse this answer
Creative Commons License