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Topic: Aldol condensation between Benzaldehyde and acetophenone  (Read 4866 times)

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Offline Sagar Hathwar

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Aldol condensation between Benzaldehyde and acetophenone
« on: January 05, 2014, 02:41:42 AM »
I was reading about Aldol condensation reactions and found the reaction between Benzaldehyde and acetophenone a bit confusing - http://en.wikipedia.org/wiki/Chalcone
Though the α-Hydrogen of aldehydes are more acidic than that of ketones, why does the α-Hydrogen of ketone(Accetophenone) attack the carbonyl oxygen of aldehyde(Benzaldehyde) whilst it should have been the other way around i.e. α-Hydrogen of aldehyde being more acidic should have attacked the carbonyl oxygen of Ketone?

Offline kriggy

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Re: Aldol condensation between Benzaldehyde and acetophenone
« Reply #1 on: January 05, 2014, 05:36:25 AM »
Because the hydrogen in benzaldehyde is not α-hydrogen. α-hydrogen is hydrogen attached to α-carbon and there is none in benzealdehyde

Offline Sagar Hathwar

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Re: Aldol condensation between Benzaldehyde and acetophenone
« Reply #2 on: January 05, 2014, 08:09:30 AM »
Oh yes! I figured it out. Thank you very much. I was being a bit too careless.

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