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Aldol condensation between Benzaldehyde and acetophenone
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Topic: Aldol condensation between Benzaldehyde and acetophenone (Read 4866 times)
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Sagar Hathwar
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Aldol condensation between Benzaldehyde and acetophenone
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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?
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kriggy
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Re: Aldol condensation between Benzaldehyde and acetophenone
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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
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https://radioisotopes.group.uochb.cz/en
Sagar Hathwar
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Re: Aldol condensation between Benzaldehyde and acetophenone
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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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Aldol condensation between Benzaldehyde and acetophenone