The following two-step synthesis gives compound J as the major product. i. NaBH4 ii. CH₂l₂, Zn(Cu) OH J

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter23: Addition To A Carbonyl
Section: Chapter Questions
Problem 48CTQ
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(i) Explain with the aid of a reaction mechanism why the synthesis is highly diastereoselective.

(ii) Draw the structures of the enantiomer, and one epimer of J, and give definitions of these terms.

The following two-step synthesis gives compound J as the major product.
i. NaBH4
ii. CH₂l₂, Zn(Cu)
Transcribed Image Text:The following two-step synthesis gives compound J as the major product. i. NaBH4 ii. CH₂l₂, Zn(Cu)
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