**Instructions:**Draw both chair conformations of the following cyclohexane. Circle the chair conformation that is lower in energy (more stable) and provide a brief explanation for your choice.**Molecular Structure:**The structure provided shows a cyclohexane ring with a propyl group (CH2CH2CH3) attached at one of the carbon atoms. The substituent is drawn with stereochemistry indicating axial positioning (bond line going down and away).**Task Explanation:**- **Chair Conformations:** Cyclohexane can adopt different conformations due to its flexibility. The chair conformations are the most stable due to minimized steric strain. - **Axial vs Equatorial Positions:** - Atoms or groups can be placed axially (parallel to the imaginary axis of the ring) or equatorially (around the equator of the ring). - Generally, bulky groups prefer to be in the equatorial position to minimize steric hindrance.**Explanation Requirement:**- Identify which conformation has the propyl group in the equatorial position.- Explain why this conformation is more stable (lower energy), typically because of reduced steric strain or 1,3-diaxial interactions.

The structure of cyclohexane can be shown in boat form or in chair form. The chair form of…

Answered: Draw both chair conformations of the…

Draw both chair conformations of the following cyclohexane. Circle the chair conformation that is lower in energy (more stable) and provide a brief explanation for your choice.

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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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

**Instructions:**

Draw both chair conformations of the following cyclohexane. Circle the chair conformation that is lower in energy (more stable) and provide a brief explanation for your choice.

**Molecular Structure:**

The structure provided shows a cyclohexane ring with a propyl group (CH2CH2CH3) attached at one of the carbon atoms. The substituent is drawn with stereochemistry indicating axial positioning (bond line going down and away).

**Task Explanation:**

- **Chair Conformations:** Cyclohexane can adopt different conformations due to its flexibility. The chair conformations are the most stable due to minimized steric strain.

- **Axial vs Equatorial Positions:**
- Atoms or groups can be placed axially (parallel to the imaginary axis of the ring) or equatorially (around the equator of the ring).
- Generally, bulky groups prefer to be in the equatorial position to minimize steric hindrance.

**Explanation Requirement:**

- Identify which conformation has the propyl group in the equatorial position.
- Explain why this conformation is more stable (lower energy), typically because of reduced steric strain or 1,3-diaxial interactions.

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what is the chair conformed and the ring that represents it? which chair conformation is the most stable?