The Raman and IR spectra of the C-Br stretching mode in the axial and
the equatorial positions of cyclohexyl bromide have been measured at r
oom temperature. The mechanism and the differences in the rate of vibr
ational dephasing of the axial and the equatorial conformers are discu
ssed. It is found that intermolecular long range transition dipole-tra
nsition dipole coupling gives the main contribution to the differences
in vibrational dephasing rate of both conformers.