State-to-state and total rotational energy transfer (RET) rate constants were measured for collisions of CN(B (2)Sigma(+),v=0,N-i=4,7,8,11) with H-2, CN(X (2)Sigma(+),v=2,N-i=4,11) with H-2 and D-2, and CN(X (2)Sigma(+),v=3,N-i=4) with NO at room temperature and under single, or near-single, collision conditions. Rate constants were also measured for electronic quenching of CN(B (2)Sigma(+),v=0,N-i=4,7,8,and 11) by H-2. In general, state-to-state RET rate constants showed very small or no even-odd alternations as the final rotational state varied. Total rate constants for CN(X (2)Sigma(+),v=2,N)/H-2, D-2 were found to decrease with increasing rotational quantum number, N. By contrast, total rate constants for CN(B (2)Sigma(+),v=0,N)/H-2 were found to be relatively independent of N. Exponential energy gap and angular momentum fitting functions were found to represent measured state-to-state RET rate constants very well and were substantially equally effective in this regard.