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Interactive video lesson plan for: Aldol, Claisen Condensation, Acetoacetic Ester & Malonic Ester Reaction Review

Activity overview:

This organic chemistry video tutorial covers synthesis problems and reaction mechanisms associated with the aldol reaction, claisen ester condensation, the acetoacetic ester reaction, and the malonic ester synthesis reaction.

In this video, the aldol reaction of acetaldehyde was used to make an alpha beta unsaturated aldehyde which is a type of michael acceptor. The claisen ester condensation reaction was used to convert ethyl acetate into the acetoacetic ester. From the acetoacetic ester, we can create different types of methyl ketones. Using the malonic ester synthesis reaction, we were able to create alpha substituted carboxylic acid molecules.

Tagged under: aldol,claisen condensation,acetoacetic ester,malonic ester reaction,aldol reaction,malonic ester,claisen,acetoacetic,substituted ketones,substituted carboxylic acid,ethyl acetate,ketones,alpha beta unsaturated aldehyde,acetaldehyde,ester,michael acceptor,aldol condensation,methyl ketones,synthesis,mechanism,reaction mechanism,organic chemistry

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