1,3- Butadiene undergoes an electrophilic addition with Hbr. Complete the steps in the mechanism to produce the product.

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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1,3- Butadiene undergoes an electrophilic addition with Hbr. Complete the steps in the mechanism to produce the product.
Br
HBr
H3C-
=CH2
H.
1) Add curved arrows for the first step.
2) Draw both the organic and inorganic intermediate
species. Include all nonbonding electrons and charges.
Select
Draw
Rings
More
Erase
Draw a curved arrow to convert the intermediate into the
product shown.
Br
Select
Draw
Rings
More
Erase
C
Br
H - Br:
MacBook Pro
Transcribed Image Text:Br HBr H3C- =CH2 H. 1) Add curved arrows for the first step. 2) Draw both the organic and inorganic intermediate species. Include all nonbonding electrons and charges. Select Draw Rings More Erase Draw a curved arrow to convert the intermediate into the product shown. Br Select Draw Rings More Erase C Br H - Br: MacBook Pro
Final product
:Br :
H,C
CH2
H
Transcribed Image Text:Final product :Br : H,C CH2 H
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