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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![**13. Draw the mechanism of the following SN1 process:**
The image shows a chemical reaction involving a cyclohexane ring.
- On the left side, there is a cyclohexane ring with a bromine substituent (Br) on the first carbon and a methyl group on the adjacent carbon.
- An arrow indicates the reaction, with ethanol (EtOH) as the reagent.
- On the right side, the product is a cyclohexane ring where the bromine has been replaced by an ethyl group bonded through an oxygen atom (OEt).
This is an example of an SN1 mechanism where the bromine leaves, forming a carbocation intermediate, and then the ethanol attacks the carbocation, resulting in the substitution product.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F104606ce-d339-4d46-8aad-1198a93a7f1a%2F6cb7ba82-d544-407c-8995-f527751c0c42%2Fkwa2nyk_processed.png&w=3840&q=75)
Transcribed Image Text:**13. Draw the mechanism of the following SN1 process:**
The image shows a chemical reaction involving a cyclohexane ring.
- On the left side, there is a cyclohexane ring with a bromine substituent (Br) on the first carbon and a methyl group on the adjacent carbon.
- An arrow indicates the reaction, with ethanol (EtOH) as the reagent.
- On the right side, the product is a cyclohexane ring where the bromine has been replaced by an ethyl group bonded through an oxygen atom (OEt).
This is an example of an SN1 mechanism where the bromine leaves, forming a carbocation intermediate, and then the ethanol attacks the carbocation, resulting in the substitution product.
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