7-55 trans-1-Bromo-2-methylcyclohexane yields the non-Zaitsev elimination product 3-methylcyclohexene on treatment with KOH. What does this result tell you about the stereochemistry of E2 reactions? CH3 .CH3 кон Br H trans-1-Bromo-2-methylcyclohexane 3-Methylcyclohexene

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter8: Alkenes: Reactions And Synthesis
Section8.SE: Something Extra
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7-55 trans-1-Bromo-2-methylcyclohexane yields the non-Zaitsev elimination
product 3-methylcyclohexene on treatment with KOH. What does this
result tell you about the stereochemistry of E2 reactions?
CH3
.CH3
кон
Br
H
trans-1-Bromo-2-methylcyclohexane
3-Methylcyclohexene
Transcribed Image Text:7-55 trans-1-Bromo-2-methylcyclohexane yields the non-Zaitsev elimination product 3-methylcyclohexene on treatment with KOH. What does this result tell you about the stereochemistry of E2 reactions? CH3 .CH3 кон Br H trans-1-Bromo-2-methylcyclohexane 3-Methylcyclohexene
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