Q42: A Newman projection with eclipsed substituents is
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
Q48: Large substituents prefer to point equatorial in
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
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