(a) Give the simplified (nonaggregated) ionic structure of the enolate formed by treatment of 2,2-dimethylcyclohexanone with LDA;...
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(a) Give the simplified (nonaggregated) ionic structure of the enolate formed by treatment of 2,2-dimethylcyclohexanone with LDA; then, give the product of its directed aldol reaction with acetaldehyde following acidic workup.
(b) Two diastereomers of the product in part (a) are formed. Explain. Are they formed in equal amounts or different amounts?
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e Li Lit O CH3 CH3 CH3 Jos se on the wet for LDA CHCH CH3 HC CH3 CH3 ...View the full answer
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