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The most stable conformation of 3-bromo-2-methylpentane, viewed through the C-3 -C-4 bond (i.e., C-3 in the front, C-4 in the back): CH3 Br. H ≥_ OIV 1 III V II H H CH(CH3)2 I Br H -I IV Br HO CH3 II CH(CH3)2 CH3 CH(CH3)2 Br. H H H CH3 H H CH3 CH(CH3)2 III 우 CH3 Br CH₂CH3 V

The most stable conformation of 3-bromo-2-methylpentane, viewed through the C-3 -C-4 bond (i.e., C-3 in the front, C-4 in the back): CH3 Br. H ≥_ OIV 1 III V II H H CH(CH3)2 I Br H -I IV Br HO CH3 II CH(CH3)2 CH3 CH(CH3)2 Br. H H H CH3 H H CH3 CH(CH3)2 III 우 CH3 Br CH₂CH3 V

Organic Chemistry
Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry
Section4.4: Conformations Of Cycloalkanes
Problem 11P: Two conformations of cis-l, 3-dimethylcyclobutane are shown. What is the difference between them,...
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Viewed through the C-3 — C-4 bond, which is the most stable conformation of 3-bromo-2-methylpentane?
The most stable conformation of 3-bromo-2-methylpentane, viewed through the C-3 -C-4 bond (i.e., C-3 in the front, C-4 in the back): CH3 Br. H * H H CH(CH3)2 OVV OI III V OII I Br H H -I H IV Br H H& II CH(CH3)2 CH3 CH3 CH(CH3)2 Br H H H CH3 H H CH3 CH(CH3)2 III CH3 Br CH₂CH3 V
Transcribed Image Text:The most stable conformation of 3-bromo-2-methylpentane, viewed through the C-3 -C-4 bond (i.e., C-3 in the front, C-4 in the back): CH3 Br. H * H H CH(CH3)2 OVV OI III V OII I Br H H -I H IV Br H H& II CH(CH3)2 CH3 CH3 CH(CH3)2 Br H H H CH3 H H CH3 CH(CH3)2 III CH3 Br CH₂CH3 V
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