Lab 10 Multistep Synthesis Sequence: An Aldol Condensation, A Michael Addition

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Last updated 4:57 AM on 4/21/26
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4 Terms

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what is a condensation reaction

reaction that combines two molecules and removes some water or alcohol

2
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what happens with the aldol condensation

the alpha hydrogen of the acetone is deprotonated by the ethanol. The the deouble bond from the oxygen shift down and makes a nucleophilic double bond to that carbon. Then the nucleophile attacks the carbonyl carbon from the p-anisaldehyde. The electrons will get pushed up on the carbonyl of the p-anisaldehyde and then get turned into an alcohol. This happens twice on both alpha carbons but the it will get dehydrate, so the H from the alpha carbon will get eliminated and kick off the OH.

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what happens with michael addition

the alpha carbons of 2 molecules of dimethyl malonate will attach to both beta carbons of the dianisalacetone. The alpha carbon will be deprotonates using ethanol

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