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- What is the product formed when each dicarbonyl compound undergoes an intramolecular aldol reaction, followed by dehydration.4. Give the structures of the aldol products that form when each of the following compounds or mixtures is treated with NAOH. a) Butanal b) Cyclopentanone c) Acetophenone d)-Chlorobenzaldehyde and 2,2-dimethylcyclohexanoneDraw the product formed when each dicarbonyl compound undergoes an intramolecular aldol reaction followed by dehydration, when possible.
- What aldehyde or ketone is needed to prepare each compound by an aldol reaction?Draw the structures A, B and C for the reaction sequence below. Dehydration via an E1cb mechanism Michael Reaction Intramolecular Aldol Reaction A В КОН /ETOH / heat C КОН /ETOH КОН /ETOH16. Draw the structure of the aldol self-condensation (followed by dehydration) product for each of the following compounds. If a compound does not undergo aldol self-condensation, explain why it does not. a) || CH3CHCH₂CH T CH₂ b)
- 2) An enolate attacks an aldehyde and the resulting product is subsequently protonated. W type of reaction is this? A) a Fischer esterification B) an acid-catalyzed aldol condensation C) a base-mediated aldol condensation D) a Hell-Volhard-Zelinsky reactionExplain why ketone K undergoes aldol reactions but ketone J does not.What is the general name for the reaction product formed in an aldol addition reaction? O 1) a-hydroxy carbonyl compound 2) a.ß-hydroxy carbonyl compound O3) Y-hydroxy carbonyl compound 4) B-hydroxy carbonyl compound