Solution Found!

Solved: What products are formed when the following

Chapter 10, Problem 62P

(choose chapter or problem)

Get Unlimited Answers
QUESTION:

What products are formed when the following stereoisomer of \(2-\text{chloro}-1\),\(3-\text{dimethylcyclohexane}\) reacts with methoxide ion in a solvent that encourages \(\mathrm{S}_\mathrm{N}2 / \mathrm{E}2\) reactions:

Equation Transcription:

2-chloro-1

3-dimethylcyclohexane

SN2/E2

Text Transcription:

2-chloro-1

3-dimethylcyclohexane

S_N 2/E2

Questions & Answers

QUESTION:

What products are formed when the following stereoisomer of \(2-\text{chloro}-1\),\(3-\text{dimethylcyclohexane}\) reacts with methoxide ion in a solvent that encourages \(\mathrm{S}_\mathrm{N}2 / \mathrm{E}2\) reactions:

Equation Transcription:

2-chloro-1

3-dimethylcyclohexane

SN2/E2

Text Transcription:

2-chloro-1

3-dimethylcyclohexane

S_N 2/E2

ANSWER:

Solution 62P

Step 1 of 3

(1R, 2r, 3S)-2-chloro-1,3-dimethylcyclohexane reacts with methoxide ion undergo  reaction to give (1R,2s,3S)-2-methoxy-1,3-dimethylcyclohexane. The stereochemistry of  reaction is inversion of configuration at substituted carbon.

Add to cart


Study Tools You Might Need

Not The Solution You Need? Search for Your Answer Here:

×

Login

Login or Sign up for access to all of our study tools and educational content!

Forgot password?
Register Now

×

Register

Sign up for access to all content on our site!

Or login if you already have an account

×

Reset password

If you have an active account we’ll send you an e-mail for password recovery

Or login if you have your password back