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At first sight, this statement may not seem to be generally true, since some alcohols, such as 1-propanol, have a Debye-like, well-separated β-relaxation peak. However, it was recently found that the strong Debye process is due to the hyroxyl group, and the remainder constitutes two faster processes, attributed to the structural α-relaxation and the Johari-Golstein β-relaxation, respectively. The resolved α-relaxation is not Debye-like; its width is compatible with a KWW function having a value of (1 - n) = 0.60. See C. Hansen, F. Stickel, T. Berger, R. Richert, and E. W. Fischer, J. Chem. Phys. 107, 1086 (1997).
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