Draw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. ### Diagram DescriptionThe image presents a molecular structure of a cyclohexane ring with a thiol group (SH) attached. The structure features the following details:- **Cyclohexane Ring**: A six-membered carbon ring depicted in a hexagonal shape.- **Thiol Group (SH)**: Attached to one of the carbon atoms in the ring. The bonds to the SH group are represented using wedge-and-dash notation: - **Wedge Bond**: Indicates that the group is coming out of the plane towards the viewer. - **Dash Bond**: Shows the group going into the plane away from the viewer.### InstructionBelow the structure, a dashed box contains the text:- **"Draw a Diastereomer"**### ExplanationThe instructional text prompts the viewer to draw a diastereomer of the given structure. Diastereomers are stereoisomers that are not mirror images of each other and have multiple chiral centers. In this context, the exercise likely requires changing the stereochemistry at one or more chiral centers while maintaining the same connectivity of the atoms in the cyclohexane ring.

Diastereomers were formed by changing stereochemistry along one carbon atom.

Answered: Draw one of the possible diastereomers…

Draw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable

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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