The chair conformations of trans-1,3-dimethylcyclohexane are equal in energy.
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Q45: Cyclobutane rings adopt an envelope conformation.
Q46: The chair conformation is the most stable
Q47: An eclipsed confirmation has only steric strain.
Q48: Large substituents prefer to point equatorial in
Q49: The most stable conformation of cyclopropane is
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
Q54: A cyclohexane boat conformation is more strained
Q55: Which cyclopropane ring would be more strained
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