Chemistry
10th Edition
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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
Related questions
Question
![What will be the major product of the shown E2 reaction:
CH3
H3C-C-o
CH3
N.
ČH3
N.
N.
H.
acetonitrile
N.
N.
OC-(CH3)3
Br
ÓC-(CH3)3
A
C
O 1.A
the reaction won't occur as shown
O 2.
3. В
4. C
5. D](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F8a8bd4c6-093e-4d1c-86bd-4cc75de9936b%2F8724dafd-c9c0-4527-94bf-a7a412838819%2F363sqah_processed.jpeg&w=3840&q=75)
Transcribed Image Text:What will be the major product of the shown E2 reaction:
CH3
H3C-C-o
CH3
N.
ČH3
N.
N.
H.
acetonitrile
N.
N.
OC-(CH3)3
Br
ÓC-(CH3)3
A
C
O 1.A
the reaction won't occur as shown
O 2.
3. В
4. C
5. D
Expert Solution
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Step 1
The elimination reaction E2 is a bimolecular elimination, which has only one step. A new bond is formed to break carbon hydrogen and carbon-halogen bonds. The major product obtained from an elimination reaction is the most stable alkene compound.
Step 2
In the given reactant, hydrogen and bromine are at anti positions, hence the option C will be major product. The eliminated hydrogen is in same plane of bromine in the formed alkene.
The product formed is as follows,
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