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The Raman spectra of cyclopentene and 2,5-dihydrofuran, both in the gaseous state, were recorded from 70 to 3500 cm−1. Even the very weak ring puckering vibrations were observable. The selection rule for this normal mode is Δv=2 for the molecules studied even though the 2,5-dihydrofuran molecule is a planar molecule. The observation of these double quantum jumps can be a powerful check on the sometimes ambiguous assignment of the far-infrared transitions. It is also shown that the Raman combination and difference bands in the C–H stretching region may be useful for obtaining the ring puckering transitions.
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Durig et al. (1972) studied this question.
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