The major products of the photosensitization of 1,3‐cyclohexadiene (25–160 Torr) by benzaldehyde (4.5–5.0 Torr) at 50.0 ± 0.2 °C, using light with wavelengths > 300 nm, are the dimers trans‐cis‐trans‐tricyclo(6.4.0.02,7)dodeca‐3,11‐diene, the corresponding all cis‐isomer, exo‐, and endo‐dicyclohexadiene in the ratio 3:1:0.8:0.04, independent of substrate pressure. Traces of cyclohexene and benzene are also formed, presumably from the decomposition of excited dimers before collisional stabilization can occur. The product distribution and the kinetic features of the reaction are best explained by assuming that the photosensitization involves triplet energy transfer from benzaldehyde to 1,3‐cyclohexadiene molecules.