Large substituents prefer to point equatorial in cyclohexane chair conformations.
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Q43: The chair conformations of trans-1,4-dimethylcyclohexane are equal
Q44: Free rotation is allowed around single bonds.
Q45: Cyclobutane rings adopt an envelope conformation.
Q46: The chair conformation is the most stable
Q47: An eclipsed confirmation has only steric strain.
Q49: The most stable conformation of cyclopropane is
Q50: The chair conformations of trans-1,3-dimethylcyclohexane are equal
Q51: Axial substituents exist above and below the
Q52: The interpenetration of electron clouds from nearby
Q53: A cyclohexane twist-boat conformation is more strained
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