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Predict the product of the reaction of cis-1-bromo-3-methylcyclohexane with NaSH (using DMSO as solvent) H₂C HE H₂C O H₂C -. H₂C Hlun- Br WISH SH

Predict the product of the reaction of cis-1-bromo-3-methylcyclohexane with NaSH (using DMSO as solvent) H₂C HE H₂C O H₂C -. H₂C Hlun- Br WISH SH

Chemistry
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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**Title: Predicting the Product of a Reaction** **Objective:** To predict the product of the reaction of cis-1-bromo-3-methylcyclohexane with NaSH (using DMSO as a solvent). **Content:** In this exercise, you will predict the result of the reaction between cis-1-bromo-3-methylcyclohexane and sodium hydrosulfide (NaSH), using dimethyl sulfoxide (DMSO) as a solvent. **Options:** This reaction will yield one of the following products: 1. **Option 1:** A cyclohexane ring with methyl and sulfhydryl (SH) groups attached to adjacent carbon atoms. - Structure: - A cyclohexane ring with: - A methyl (CH₃) group attached to one carbon. - An SH group (sulfhydryl) attached to the adjacent carbon. - Displayed as follows: ``` H₂C-- / \ --H H / \ SH H₂C-- \ / --H CH₃ ``` 2. **Option 2:** A cyclohexane ring with one bromine and one methyl group attached to non-adjacent carbon atoms. - Structure: - A cyclohexane ring with: - A bromine (Br) group attached to one carbon. - A methyl (CH₃) group attached to another, non-adjacent carbon. - Displayed as follows: ``` H₂ -- / \ ----H H / \ Br H₂C \ / -- CH₃ ``` 3. **Option 3:** A cyclohexane ring with one bromine and one 3-methylsulfanyl group attached. - Structure: - A cyclohexane ring with: - A bromine (Br) group attached to one carbon. - A methyl 3-sulfanyl (SCH₃) group attached to another carbon. - Displayed as follows: ``` H₂ -- / \ ----H H / \ Br SH -- \ / -- CH₃ ``` 4. **Option 4:** A cyclohexane ring with one methyl and one sulfhyd
Transcribed Image Text:**Title: Predicting the Product of a Reaction** **Objective:** To predict the product of the reaction of cis-1-bromo-3-methylcyclohexane with NaSH (using DMSO as a solvent). **Content:** In this exercise, you will predict the result of the reaction between cis-1-bromo-3-methylcyclohexane and sodium hydrosulfide (NaSH), using dimethyl sulfoxide (DMSO) as a solvent. **Options:** This reaction will yield one of the following products: 1. **Option 1:** A cyclohexane ring with methyl and sulfhydryl (SH) groups attached to adjacent carbon atoms. - Structure: - A cyclohexane ring with: - A methyl (CH₃) group attached to one carbon. - An SH group (sulfhydryl) attached to the adjacent carbon. - Displayed as follows: ``` H₂C-- / \ --H H / \ SH H₂C-- \ / --H CH₃ ``` 2. **Option 2:** A cyclohexane ring with one bromine and one methyl group attached to non-adjacent carbon atoms. - Structure: - A cyclohexane ring with: - A bromine (Br) group attached to one carbon. - A methyl (CH₃) group attached to another, non-adjacent carbon. - Displayed as follows: ``` H₂ -- / \ ----H H / \ Br H₂C \ / -- CH₃ ``` 3. **Option 3:** A cyclohexane ring with one bromine and one 3-methylsulfanyl group attached. - Structure: - A cyclohexane ring with: - A bromine (Br) group attached to one carbon. - A methyl 3-sulfanyl (SCH₃) group attached to another carbon. - Displayed as follows: ``` H₂ -- / \ ----H H / \ Br SH -- \ / -- CH₃ ``` 4. **Option 4:** A cyclohexane ring with one methyl and one sulfhyd
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