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Solved: What products are formed when the following
Chapter 10, Problem 62P(choose chapter or problem)
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.