Reaction of a large excess of H2S with 2 mol of Cr-.(CO)(3)C5Me5 yields HCr(CO)(3)C5Me5 and HSCr(CO)(3)C5Me5. Kinetic studies of this reaction show two reaction pathways are followed. At; pressures of CO above 10-15 atm and temperatures less than or equal to 10 degrees C, a third-order rate law d[P]/dt = k(3rd order)[Cr-.(CO)(3)C5Me5](2)[H2S] is followed. The value of the third-order rate constant 70 +/- 5 M-2 s(-1) is essentially independent of temperature in the range -30 to +10 degrees C. As the pressure of CO is reduced, mixed-order kinetics is followed, and under argon atmosphere the reaction obeys the following second-order rate law: d[P]/dt = k(2nd order)[Cr-.(CO)(3)C5Me5][H2S]. The value of k(2nd order) was found to be 0.20 +/- 0.05 M-1 s(-1) at 1 degrees C and 0.30 +/-0.05 M-1 s(-1) at 10 degrees C. This reaction channel is proposed to proceed by rate-determining ligand substitution and formation of the hydrogen sulfide substituted radical complex Cr-.(H2S)(CO)(2)C5Me5. The rate of ligand substitution of Cr-.(CO)(3)C5Me5 by PMe2Ph yielding the phosphine-substituted radical Cr-.(PMe2Ph)(CO)(2)C5Me5 has been reinvestigated and shown to have rate constants and activation parameters similar to those proposed for rate-determining formation of Cr-.(H2S)(CO)(2)C5Me5. A reasonable fit to data at intermediate pressures of CO is obtained at T less than or equal to 10 degrees C by combining the 17e(-) second order and 19e(-) third-order mechanisms for oxidative addition. The complex HSCr(CO)(3)C5Me5 can react with an additional 2 mol of Cr-.(CO)(3)C5Me5 yielding HCr(CO)(3)C5Me5 + C5Me5(CO)(2)Cr = S = Cr(CO)(2)C5Me5 + 2CO. At a temperature of 50 degrees C under 1 atm of CO the net reaction 4(.)Cr(CO)(3)C5Me5 + H2S --> 2HCr(CO)(3)C5Me5 + C5Me5(CO)(2)Cr = S = Cr(CO)(2)C5Me5 + 2CO occurs within minutes without formation of detectable amounts of HSCr(CO)(3)C5Me5.