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Last Update: 02/06/2025 03:27 AM

Current Deck: AnKing-MCAT::MileDown's MCAT Decks::Organic Chemistry

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#AK_MCAT_v2::#KahnAcademy::OChem::Aldehydes-and-Ketones #AK_MCAT_v2::#Kaplan::Organic-Chemistry::Ch-07-Aldehydes-and-Ketones-II:-Enolates #AK_MCAT_v2::MileDown::OChem::Aldehydes_and_Ketones

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Commit #341155

Here is the big picutre– if you see an acryl group and you use an enolate to try to do an adol reaction (1,2 [one being the negative charge on the enolate, 2 being the carbony of the thing your atacking]) then you will attack the beta carbon, and you will form a 1,4 product.

For aldo addition you get a hydroxly group, for micheal adition you get a carbonyl on the 4

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