Provide the missing compounds for each step in the following synthesis. Please use Br as your leaving group, should you require one. Be sure to show stereochemistry explicitly where necessary, using wedges and dashes. Br CH3 NaOCH3 Br2 H A Br CH3 CH3OH H3C a "2-bromo- + enantiomer 3-methylpentane" Synthetic target

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter14: Elimination
Section: Chapter Questions
Problem 35CTQ
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Draw compound a and b

Provide the missing compounds for each step in the following synthesis. Please use Br as your leaving group, should you require one. Be sure to show
stereochemistry explicitly where necessary, using wedges and dashes.
Br
CH3
H
Br2
NaOCH3
A
Br
CH3
CH3OH
H3C
+ enantiomer
a "2-bromo-
3-methylpentane"
Synthetic target
LI
Transcribed Image Text:Provide the missing compounds for each step in the following synthesis. Please use Br as your leaving group, should you require one. Be sure to show stereochemistry explicitly where necessary, using wedges and dashes. Br CH3 H Br2 NaOCH3 A Br CH3 CH3OH H3C + enantiomer a "2-bromo- 3-methylpentane" Synthetic target LI
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