Curved arrows are used to illustrate the flow of electrons. Using the provided starting structures, draw the curved electron-pushing arrows for a nucleophilic substitution or elimination reaction and draw the resulting products. Be sure to account for all bond-breaking and bond-making steps. Base Θ HH H H HH :Br: H H H Select to Add Arrows Base, 80 °C (CH3)2SO (DMSO) Select to Draw Product H

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution
Section16.SE: Something Extra
Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...
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Curved arrows are used to illustrate the flow of electrons. Using the provided starting
structures, draw the curved electron-pushing arrows for a nucleophilic substitution
or elimination reaction and draw the resulting products.
Be sure to account for all bond-breaking and bond-making steps.
Base
Θ
HH
H
H
HH
:Br:
H
H
H
Select to Add Arrows
Base, 80 °C
(CH3)2SO (DMSO)
Select to Draw Product
H
Transcribed Image Text:Curved arrows are used to illustrate the flow of electrons. Using the provided starting structures, draw the curved electron-pushing arrows for a nucleophilic substitution or elimination reaction and draw the resulting products. Be sure to account for all bond-breaking and bond-making steps. Base Θ HH H H HH :Br: H H H Select to Add Arrows Base, 80 °C (CH3)2SO (DMSO) Select to Draw Product H
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