What is the most stable conformation of trans-1-tert-butyl-4-methylcyclohexane?

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SUMMARY

The most stable conformation of trans-1-tert-butyl-4-methylcyclohexane is when both the tert-butyl group and the methyl group are in equatorial positions. This configuration minimizes steric strain and torsional strain, leading to greater stability. The twist boat conformation is not the most stable arrangement for this molecule. The discussion confirms that the equatorial positioning of both groups is optimal.

PREREQUISITES
  • Understanding of cyclohexane conformations
  • Knowledge of steric strain and torsional strain
  • Familiarity with trans-1-tert-butyl-4-methylcyclohexane structure
  • Basic principles of organic chemistry
NEXT STEPS
  • Study cyclohexane chair conformations in detail
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Chemistry students, organic chemists, and anyone studying molecular conformations and stability in organic compounds.

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The most stable conformation of trans-1-tert-butyl-4-methylcyclohexane is the one in which:
A- the tert-butyl group is axial and the methyl group is equatorial
B- the methyl group is axial and the tert-butyl group is equatorial
C- both groups are axial
D- both groups are equatorial
E- the molecule is in the twist boat conformation
o:)
 
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I get D.. can someone confirm me?
Reasoning: in trans-1-tert-butyl-4-methylcyclobutane both the tert-butyl and the c-4 methyl group are equatorial
 
Yup. Not so hard, is it?
 

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