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In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:
- a)Axial and equatorial
- b)Equatorial and equatorial
- c)Equatorial and axial
- d)Axial and axial
Correct answer is option 'C'. Can you explain this answer?
Most Upvoted Answer
In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexan...
Explanation:
The stability of a cyclohexane molecule depends on the orientation of its substituents. The most stable conformation is the one in which the bulky substituents are positioned in equatorial positions, while the smaller substituents are in axial positions.
In trans-1-t-butyl-3-methylcyclohexane, the t-butyl group is the bulkier substituent and should be positioned in the equatorial position, while the smaller methyl group should be in the axial position. This orientation minimizes steric hindrance and maximizes stability.
Therefore, the correct answer is option C, which states that the substituents at C-1 and C-3 are equatorial and axial, respectively.
The stability of a cyclohexane molecule depends on the orientation of its substituents. The most stable conformation is the one in which the bulky substituents are positioned in equatorial positions, while the smaller substituents are in axial positions.
In trans-1-t-butyl-3-methylcyclohexane, the t-butyl group is the bulkier substituent and should be positioned in the equatorial position, while the smaller methyl group should be in the axial position. This orientation minimizes steric hindrance and maximizes stability.
Therefore, the correct answer is option C, which states that the substituents at C-1 and C-3 are equatorial and axial, respectively.
Community Answer
In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexan...
Even though if both equatorial are stable but the question is compound is trans ......correct option Cany doubt?????
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In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer?
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In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer? for Chemistry 2024 is part of Chemistry preparation. The Question and answers have been prepared according to the Chemistry exam syllabus. Information about In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer? covers all topics & solutions for Chemistry 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer?.
In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer? for Chemistry 2024 is part of Chemistry preparation. The Question and answers have been prepared according to the Chemistry exam syllabus. Information about In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer? covers all topics & solutions for Chemistry 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer?.
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In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer?, a detailed solution for In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer? has been provided alongside types of In the most stable conformation of trans-1-t-butyl-3-methylcyclo hexane, the subst ituents at C-1 and C-3, respectively, are:a)Axial and equatorialb)Equatorial and equatorialc)Equatorial and axiald)Axial and axialCorrect answer is option 'C'. Can you explain this answer? theory, EduRev gives you an
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