A general survey is given of the relations between the anisotropy of t
he Raman scattering intensities of a crystal and the effective Raman t
enser of the molecule corresponding to the molecular vibration in ques
tion. Some of the Raman tensors determined by the use of these relatio
ns are discussed. The Raman tenser assignable to the CH2 scissoring vi
bration at 1400 cm(-1) is found to be not transferable between differe
nt molecules in different crystals. However, the amide I Raman tenser
of the peptide group is found to remain nearly unchanged on going from
a dipeptide crystal to a synthetic polypeptide fiber. The usefulness
of such knowledge in determining the orientation of a functional group
in a biological system is suggested.