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Explain Cyclobutane
Cyclobutane undergoes an interconversion of puckered forms analogous to the chair interconversion of cyclohexane. This interchanges axial and equatorial groups. Thus, one conformation of trans1,2-dimethylcyclobutane-the more stable conformation-has diequatorial substituents, and the other-the less stable conformation-has diaxial substituents
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n-propyl acetate evaporates rapidly when exposed to air,but water does not.Explain
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