The photosensitized electron-transfer oxidation of a series of ethyl sulfides RSEt (1, R = C 12 H 25 ; 2, PhCH 2 CH 2 ; 3, PhCH 2 ; 4, PhCMe 2 ; 5, Ph 2 CH) has been examined in acetonitrile and the product distribution discussed on the basis of the mechanisms proposed. In nitrogen-flushed solutions, cleaved alcohols and alkenes are formed, whereas under oxygen, in reactions that are 10-70 times faster, sulfoxides and cleaved aldehydes and ketones are formed in addition to the aforementioned products. Two sensitizers are compared, 9,10-dicyanoanthracene (DCA) and 2,4,6-triphenylpyrylium tetrafluoroborate (TPP + BF 4 -), the former giving a higher proportion of the sulfoxide, the latter of cleaved carbonyls. The