What is the appropriate systematic name for the compound below? (15,3R)-1-(1,1-dimethylethyl)-3-mercaptocyclohexane O (1R,3R)-3-tert-butylcyclohexanethiol (1R,3S)-3-(1,1-dimethylethyl)cyclohexanethiol cis-3-tert-butylcyclohexanethiol
What is the appropriate systematic name for the compound below? (15,3R)-1-(1,1-dimethylethyl)-3-mercaptocyclohexane O (1R,3R)-3-tert-butylcyclohexanethiol (1R,3S)-3-(1,1-dimethylethyl)cyclohexanethiol cis-3-tert-butylcyclohexanethiol
Chemistry
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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:**
What is the appropriate systematic name for the compound below?
[Image of chemical compound structure]
**Options:**
A. (1S,3R)-1-(1,1-dimethylethyl)-3-mercaptocyclohexane
B. (1R,3R)-3-tert-butylcyclohexanethiol
C. (1R,3S)-3-(1,1-dimethylethyl)cyclohexanethiol
D. cis-3-tert-butylcyclohexanethiol
**Compound Structure Explanation:**
The image presents a cyclohexane ring with two substituents. The substituents are positioned in such a way that one is an SH (thiol) group and the other is a tert-butyl group. The stereochemistry and exact positioning of these groups are critical to determining the compound's systematic name.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc0f85ff8-2ea0-4d43-a0c0-84de96cc63b8%2F6e7cf72b-a3ff-42f4-9f86-50bd877ed7b6%2Fb3m4z2r_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Question:**
What is the appropriate systematic name for the compound below?
[Image of chemical compound structure]
**Options:**
A. (1S,3R)-1-(1,1-dimethylethyl)-3-mercaptocyclohexane
B. (1R,3R)-3-tert-butylcyclohexanethiol
C. (1R,3S)-3-(1,1-dimethylethyl)cyclohexanethiol
D. cis-3-tert-butylcyclohexanethiol
**Compound Structure Explanation:**
The image presents a cyclohexane ring with two substituents. The substituents are positioned in such a way that one is an SH (thiol) group and the other is a tert-butyl group. The stereochemistry and exact positioning of these groups are critical to determining the compound's systematic name.
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