c. The following molecule will undergo E2 elimination even though it looks very similar to the cyclohexane derivative above. Predict the product of the reaction and explain the difference in E2 reactivities (why does it occur on the molecule below and not on the cyclohexane derivative?) Me Me Me OTS Me ''Et NAOMe
c. The following molecule will undergo E2 elimination even though it looks very similar to the cyclohexane derivative above. Predict the product of the reaction and explain the difference in E2 reactivities (why does it occur on the molecule below and not on the cyclohexane derivative?) Me Me Me OTS Me ''Et NAOMe
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter14: Elimination
Section: Chapter Questions
Problem 3E
Related questions
Question
Need help with part c. The cyclohexane derivative shown below does not undergo E2 elimination. what do we do after we roate the bond roate the bond.
![Me Me
Me
Me Me
OTS
OTS
Me ''Et
"Et
a. Complete the chair representation
of the substrate. You must show all
groups (including hydrogen atoms)
to receive credit.
b. Using your chair representation above, explain why E2 elimination does not occur.
c. The following molecule will undergo E2 elimination even though it looks very similar to
the cyclohexane derivative above. Predict the product of the reaction and explain the
difference in E2 reactivities (why does it occur on the molecule below and not on the
cyclohexane derivative?)
E2 conditions
no reaction
NaOMe
OTS](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F8720c98b-bd87-42fd-b648-a55f3d973b50%2Ffeda8518-fee8-4707-8f40-6fcdd443aa6a%2Fve3bj3_processed.png&w=3840&q=75)
Transcribed Image Text:Me Me
Me
Me Me
OTS
OTS
Me ''Et
"Et
a. Complete the chair representation
of the substrate. You must show all
groups (including hydrogen atoms)
to receive credit.
b. Using your chair representation above, explain why E2 elimination does not occur.
c. The following molecule will undergo E2 elimination even though it looks very similar to
the cyclohexane derivative above. Predict the product of the reaction and explain the
difference in E2 reactivities (why does it occur on the molecule below and not on the
cyclohexane derivative?)
E2 conditions
no reaction
NaOMe
OTS
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