The products of the gas-phase reactions of the OH radical with n-penta
ne and [H-2(12)]pentane have been studied at 296 +/- 2 K and 740 Torr
total pressure of N-2-O-2 diluent gas in the presence of NO. Direct ai
r sampling, atmospheric-pressure ionisation tandem mass spectrometry s
howed the formation of the previously predicted C-5-hydroxycarbonyl pr
oduct, together with pentanones. The effect of varying the O-2 concent
ration on the C-5-hydroxycarbonyl and pentanones was consistent with t
he hydroxy-carbonyl being the product formed after isomerisation of th
e pentan-2-oxyl radical. Gas chromatographic analyses of pentan-2-one
and pentan-3-one and pentan-2-yl and pentan-3-yl nitrates allowed rate
constants for the decomposition and isomerisation reactions of the pe
ntan-2-oxyl and pentan-3-oxyl radicals, relative to their reactions wi
th O-2, to be determined.