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Draw the isomer of the compound below that can have all the groups equatoria wedges and/or dashes AND in the chair and flipped chair (so 3 structures total). O-H CH3 CI 123 EQ qM

Draw the isomer of the compound below that can have all the groups equatoria wedges and/or dashes AND in the chair and flipped chair (so 3 structures total). O-H CH3 CI 123 EQ qM

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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**Educational Resource on Cyclohexane Chair Conformations** Chemical Structure and Task: The image presents a cyclohexane ring with three substituents: - A hydroxyl group (OH) is attached. - A chlorine atom (Cl) is attached. - A methyl group (CH₃) is attached. Instruction for the Exercise: - Draw the isomer of the given compound that can have all the groups equatorial. - Use wedges and/or dashes to represent stereochemistry in your drawings. - Illustrate both the regular chair conformation and the flipped chair conformation. - Present three structures in total. **Understanding Chair Conformations:** The chair conformation is the most stable form of cyclohexane due to minimized steric strain, allowing for the proper placement of substituents. The positions around the cyclohexane ring can be either axial (perpendicular to the plane) or equatorial (around the plane). - **Equatorial Position:** Offers more spatial freedom, reducing steric hindrance. - **Axial Position:** Can generate more steric strain if bulky groups are present. **Goal and Learning Outcome:** By completing this exercise, students will gain an understanding of stereochemistry and the stability associated with different conformers of cyclohexane. This task enhances visualization skills and comprehension of molecular geometry, crucial for organic chemistry studies.
Transcribed Image Text:**Educational Resource on Cyclohexane Chair Conformations** Chemical Structure and Task: The image presents a cyclohexane ring with three substituents: - A hydroxyl group (OH) is attached. - A chlorine atom (Cl) is attached. - A methyl group (CH₃) is attached. Instruction for the Exercise: - Draw the isomer of the given compound that can have all the groups equatorial. - Use wedges and/or dashes to represent stereochemistry in your drawings. - Illustrate both the regular chair conformation and the flipped chair conformation. - Present three structures in total. **Understanding Chair Conformations:** The chair conformation is the most stable form of cyclohexane due to minimized steric strain, allowing for the proper placement of substituents. The positions around the cyclohexane ring can be either axial (perpendicular to the plane) or equatorial (around the plane). - **Equatorial Position:** Offers more spatial freedom, reducing steric hindrance. - **Axial Position:** Can generate more steric strain if bulky groups are present. **Goal and Learning Outcome:** By completing this exercise, students will gain an understanding of stereochemistry and the stability associated with different conformers of cyclohexane. This task enhances visualization skills and comprehension of molecular geometry, crucial for organic chemistry studies.
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Step 1: Interpretation of given problem

Given compound is cyclohexane derivative.

We have to draw most stable conformation of this compound i.e. chair conformation with all groups equatorial. 

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