To gain insight into a recent observation that the prominent, Debye-type relaxation process observed for a primary alcohol may not be the alpha-relaxation process associated with molecular diffusion of a liquid [Europhys. Lett. 40, 549 (1997), J. Chem. Phys. 107, 1086 (1997)], the dielectric spectra of an uncrystallizable secondary alcohol, 5-methyl-2-hexanol, has been investigated by broadband spectroscopy. Measurements made over a temperature range from 110 to 298 K showed that three relaxation processes occur. Processes I and II have a non-Arrhenius variation of the relaxation rate with temperature, and process III an Arrhenius. Only process I, the slowest of the three, has a single relaxation rate, the other two, a broad distribution. The contribution to permittivity from process II was 0.8, i.e., similar to 3% of the static permittivity, and from process III, the fastest was 0.1, i.e., similar to 0.3%. It is argued that the mechanism of process I is the breaking followed by dipolar reorientation and reforming of the H-bonds in the intermolecularly H-bonded structure, and process II is that of the orientation of the other dipolar groups, such as the -OR group. Process III is the usual Johari-Goldstein process. For 5-methyl-2-hexanol, the mode-coupling and another theory by Souletie and Bertrand [J. Phys. I 1, 1627 (1991)] seem to agree with the relaxation rate of processes I and II, and predict temperatures for 10(-4) Hz relaxation rate, within a few degrees of that expected. (C) 2000 American Institute of Physics. [S0021-9606(00)51705-X].