Ion-molecule reactions of some isomeric [C-6,H-5,O](+) ions with metha
nol, acetonitrile, acetone, benzene and toluene were studied in a trip
le quadrupole mass spectrometer. The C6H5O+ ion (I) formed adducts wit
h the above molecules, whereas the isomeric HOC6H4+ (II) ions reacted
with methanol to give (HO)(2)C6H4+.. This reaction was diagnostic for
ions of structure II. Isomers I and II also reacted differently with a
cetone forming C6H5O+C3H4 and HOC6H4O+H2, respectively. No major diffe
rences were found in the reactivities of ortho-, meta- and para-hydrox
yphenyl ions, although the latter two produced a greater relative abun
dance of adducts with toluene.