8. Organometallic reagents, such as organolithium (RLi), Gilman or Organo-cuprates (R2)CuLi) and Grignard (R MgBr), have been known to transform ketones and aldehyde molecules. Pages 1032-1033 show these reagents can modify acid chlorides, acid anhydrides and esters. OR Given the reactions below, provide the missing products, indicate the likely intermediates and explain all routes yield a alcohol. ÇI 1. LİCH3, ether, rt 2. H;O* 1. CH,CH,MgBr, diethyl ether 2. НС, Н,О 1. (PHCH2),CuLi, THF Ph 2. HCС, Н,О

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter10: Alcohols
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Problem 10.50P
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8. Organometallic reagents, such as organolithium (RLi), Gilman or Organo-cuprates ((R2)CuLi) and
Grignard (R MgBr), have been known to transform ketones and aldehyde molecules. Pages 1032-1033
show these reagents can modify acid chlorides, acid anhydrides and esters.
OR
Given the reactions below, provide the missing products, indicate the likely intermediates and explain all
routes yield a
alcohol.
1. LİCH3, ether, rt
2. H;O*
1. CH;CH,MgBr,
diethyl ether
2. HС, Н,О
1. (PHCH2),CuLi, THF
Ph
2. HС, Н,О
Transcribed Image Text:8. Organometallic reagents, such as organolithium (RLi), Gilman or Organo-cuprates ((R2)CuLi) and Grignard (R MgBr), have been known to transform ketones and aldehyde molecules. Pages 1032-1033 show these reagents can modify acid chlorides, acid anhydrides and esters. OR Given the reactions below, provide the missing products, indicate the likely intermediates and explain all routes yield a alcohol. 1. LİCH3, ether, rt 2. H;O* 1. CH;CH,MgBr, diethyl ether 2. HС, Н,О 1. (PHCH2),CuLi, THF Ph 2. HС, Н,О
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