4. Clearly draw both Chair Conformations. of the following molecule Spratn 5. for the Molecule in Question 4 Circle the lowest energy Chair conformant. 2
4. Clearly draw both Chair Conformations. of the following molecule Spratn 5. for the Molecule in Question 4 Circle the lowest energy Chair conformant. 2
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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**4. Clearly draw both Chair Conformations of the following molecule:**
The image includes a hexagon representing a cyclohexane ring with two substituents. One substituent is shown as a wedge, indicating it is above the plane of the ring, and the other substituent is indicated with dashed lines, meaning it is below the plane of the ring.
**5. For the molecule in Question 4, circle the lowest energy Chair Conformation.**
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### Explanation:
The task involves drawing the two possible chair conformations for a substituted cyclohexane molecule and identifying the one with the lower energy. Chair conformations are the most stable conformations for cyclohexanes due to minimal steric hindrance and torsional strain. The substituents can be axial (perpendicular to the plane of the ring) or equatorial (in the plane of the ring), and typically, the equatorial position is favored for bulky groups to minimize steric hindrance."
Transcribed Image Text:### Transcription for Educational Website
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**4. Clearly draw both Chair Conformations of the following molecule:**
The image includes a hexagon representing a cyclohexane ring with two substituents. One substituent is shown as a wedge, indicating it is above the plane of the ring, and the other substituent is indicated with dashed lines, meaning it is below the plane of the ring.
**5. For the molecule in Question 4, circle the lowest energy Chair Conformation.**
---
### Explanation:
The task involves drawing the two possible chair conformations for a substituted cyclohexane molecule and identifying the one with the lower energy. Chair conformations are the most stable conformations for cyclohexanes due to minimal steric hindrance and torsional strain. The substituents can be axial (perpendicular to the plane of the ring) or equatorial (in the plane of the ring), and typically, the equatorial position is favored for bulky groups to minimize steric hindrance.
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