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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Question
Draw both the SN1 and E1 products of attached reaction.
![Br
H20
1](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb0fcc0d3-e645-47eb-b003-774e71839f74%2F9e4b7c0f-ebe0-40f1-a853-97b3dafd6723%2Flxzedfb.png&w=3840&q=75)
Transcribed Image Text:Br
H20
1
Expert Solution
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Step 1: Sn1 product
SN1 reaction is substitution nucleophilic unimolecular.
In this type of reaction there are two steps involved in which formation of carbocation is an intermediate step and also the rate determining step. Bond breaks between the leaving group and the organic moiety such that the bond pair of electrons are drawn towards leaving group resulting in carbocation.
Now the attack of nucleophile on carbocation takes place quickly.
The reaction is:
Mechanism:
The product formed is 1-methylcyclohexanol.
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