H NaOH HO- Br H. H. Treatment of trans-2-bromocyclohexanol with NaOH yields 1,2-epoxycyclohexane. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions :ö: :0: :Br. `H :Br:

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
Chapter8: Haloalkanes, Halogenation, And Radical Reactions
Section: Chapter Questions
Problem 8.28P
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NaOH
OH
Br
H.
`H
Treatment of trans-2-bromocyclohexanol with NaOH yields 1,2-epoxycyclohexane. Draw curved arrows to show the movement of electrons in
this step of the reaction mechanism.
Arrow-pushing Instructions
:ö:
-H
`H.
:Br:
Transcribed Image Text:NaOH OH Br H. `H Treatment of trans-2-bromocyclohexanol with NaOH yields 1,2-epoxycyclohexane. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions :ö: -H `H. :Br:
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