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Which one of the following is the most s...

Which one of the following is the most stable conformer?

A

B

C

D

Text Solution

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The correct Answer is:
To determine which conformer is the most stable among the given options (A, B, C, and D), we need to analyze the interactions present in each conformer. The stability of a conformer is influenced by the presence of attractive and repulsive interactions between the substituents on the carbon atoms. ### Step-by-Step Solution: 1. **Analyze Conformer A:** - Structure: CH3 - H - OH (front carbon) and OH - CH3 (back carbon). - Interactions: The two CH3 groups are 180 degrees apart, and the two OH groups are also 180 degrees apart. - Conclusion: There are no steric hindrance or repulsive interactions. This conformer is relatively stable due to the absence of interactions. 2. **Analyze Conformer B:** - Structure: CH3 - H (front carbon) and H - CH3 - OH (back carbon). - Interactions: There is one gauche interaction (repulsive) between CH3 and OH, but there is also the potential for hydrogen bonding between the OH groups. - Conclusion: The attractive hydrogen bonding partially offsets the repulsive interaction, making this conformer less stable than A. 3. **Analyze Conformer C:** - Structure: CH3 - OH - H (front carbon) and CH3 - OH - H (back carbon). - Interactions: There is one hydrogen bonding interaction (attractive) and no gauche interactions. - Conclusion: The presence of hydrogen bonding without any repulsive interactions makes this conformer more stable than A and B. 4. **Analyze Conformer D:** - Structure: OH - CH3 - OH - CH3 - H. - Interactions: There is one gauche interaction (repulsive) present. - Conclusion: The presence of a repulsive interaction makes this conformer less stable. 5. **Comparison of Stability:** - Conformer A: No interactions (stable). - Conformer B: One repulsive and one attractive interaction (less stable). - Conformer C: One attractive interaction and no repulsive interactions (most stable). - Conformer D: One repulsive interaction (least stable). ### Final Conclusion: The conformer with the highest amount of attractive interactions and the lowest amount of repulsive interactions is Conformer C. Therefore, the most stable conformer is **option C**. ---

To determine which conformer is the most stable among the given options (A, B, C, and D), we need to analyze the interactions present in each conformer. The stability of a conformer is influenced by the presence of attractive and repulsive interactions between the substituents on the carbon atoms. ### Step-by-Step Solution: 1. **Analyze Conformer A:** - Structure: CH3 - H - OH (front carbon) and OH - CH3 (back carbon). - Interactions: The two CH3 groups are 180 degrees apart, and the two OH groups are also 180 degrees apart. - Conclusion: There are no steric hindrance or repulsive interactions. This conformer is relatively stable due to the absence of interactions. ...
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