The reactivity of 9-substituted 10-methyl-9,10-dihydroacridirie (AcrHR) in the reactions with hydride accepters (A) such as p-benzoquinone derivatives and tetracyanoethylene (TCNE) in acetonitrile varies significantly spanning a range of 10(7) starting from R = H to Bu' and CMe2COOMe. Comparison of the large variation in the reactivity of the hydride transfer reaction with that of the deprotonation of the radical cation (AcrHR(.+)) determined independently indicates that the large variation in the reactivity is attributed mainly to that of proton transfer from AcrHR(.+) to A(.-) following the initial electron transfer from AcrHR to A. The overall hydride transfer reaction from AcrHR to A therefore proceeds via sequential electron-proton-electron transfer in which the initial electron transfer to give the radical ion pair (AcrHR(.+) A(.-)) is in equilibrium and the proton transfer from AcrHR(.+) to A(.-) is the rate-determining step. Charge-transfer complexes are shown to be formed in the course of the hydride transfer reactions from AcrHR to p-benzoquinone derivatives. A. negative temperature dependence was observed for the rates of hydride transfer reactions from AcrHR (R H, Me, and CH2Ph) to 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) in chloroform (the lower the temperature, the faster the rate) to afford the negative activation enthalpy (Delta H double dagger(obs) = -32, -4, and -13 kJ mol(-1), respectively). Such a negative Delta H double dagger(obs), value indicates clearly that the CT complex lies along the reaction pathway of the hydride transfer reaction via sequential electron-proton-electron transfer and does not enter merely through a side reaction that is indifferent to the hydride transfer reaction. The Delta H double dagger(obs) value increases with increasing solvent polarity from a negative value (-13 kJ mol(-1)) in chloroform to a positive value (13 kJ mol(-1)) in benzonitrile as the proton-transfer rate from AcrHR(.+) to DDQ(.-) may be slower.