a) Using your knowledge of organic reaction mechanisms, explain the formation of EACH product (A,B) in the following reaction. This will require you to write out MULTIPLE mechanisms (i.e. each product comes from a different reaction pathway). Hint: all reaction pathways start from the same intermediate: NaH is a strong base but cannot deprotonate an sp3 C-H bond! он он 1) NaH (0.5 equiv) Br 2) H20 A B b) Briefly explain why there is no epoxide (formed via an intramolecular substitution reaction) in the product mixture of the above reaction?
a) Using your knowledge of organic reaction mechanisms, explain the formation of EACH product (A,B) in the following reaction. This will require you to write out MULTIPLE mechanisms (i.e. each product comes from a different reaction pathway). Hint: all reaction pathways start from the same intermediate: NaH is a strong base but cannot deprotonate an sp3 C-H bond! он он 1) NaH (0.5 equiv) Br 2) H20 A B b) Briefly explain why there is no epoxide (formed via an intramolecular substitution reaction) in the product mixture of the above reaction?
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...
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Transcribed Image Text:a) Using your knowledge of organic reaction mechanisms, explain the formation of
EACH product (A,B) in the following reaction. This will require you to write out MULTIPLE
mechanisms (i.e. each product comes from a different reaction pathway). Hint: all reaction
pathways start from the same intermediate: NaH is a strong base but cannot deprotonate an sp3
C-H bond!
OH
он
1) NaH
(0.5 equiv)
Br
+
2) H20
A
B
b) Briefly explain why there is no epoxide (formed via an intramolecular substitution reaction) in
the product mixture of the above reaction?
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