The relative BrOnsted-acid strengths of H-[Al]ZSM-5, H-[Fe]ZSM-5, H-[B]ZSM-5, silicalite, P-SPP, tungstated zirconia, ZrO2, and -Al2O3 were studied using H-D exchange with toluene and chlorobenzene. Temperature programmed desorption (TPD) of toluene-h(8) and chlorobenzene-h(5) from the deuterated forms of H-[Al]ZSM-5, H-[Fe]ZSM-5, and P-SPP demonstrated that the temperature at which H-D exchange rates become significant change with the proton affinity of the aromatic molecule and the strength of the BrOnsted sites. The steady-state, gas-phase reaction between D2O and the aromatic molecules were consistent with the TPD results and allowed the BrOnsted-acid site strengths to be ordered as follows: H-[Al]ZSM-5>H-[Fe]ZSM-5>tungstated zirconia>P-SPP>H-[B]ZSM-5. H-D exchange was also observed at high temperatures with ZrO2 and -Al2O3 but it appears that the reaction mechanism with these Lewis acids is different because reaction with toluene and chlorobenzene occur at nearly the same temperature. It is suggested that the H-D exchange reaction with simple aromatic molecules is a useful way to probe BrOnsted acidity in solids. [GRAPHICS]