Five oxygenated carbon-centered free radical reactions with nitrogen dioxide (NO2) have been studied in direct time-resolved measurements. Experiments were conducted in a temperature-controlled flow tube reactor coupled to a 193 nm exciplex laser photolysis and a resonance gas lamp photoionization mass spectrometer. Reactions were investigated under pseudofirst-order conditions, with the NO2 concentrations of the experiments in great excess over the initial radical concentrations ([R](0) << [NO2]). The study consists of the three isomeric C2H5O radicals (CH3CHOH, CH2CH2OH, and CH3OCH2), and the CH2OH and CH3CO radical reactions with NO2 and, hence, includes the three smallest hydroxyalkyl radical species (CH2OH, CH2CH2OH, and CH3CHOH). The obtained rate coefficients are high with the temperature-dependent rate coefficients given by a formula k(T) = k(300K) X (T/300 K)(-n) as (in units of cm(3) molecule(-1) s(-1)): k(CH2OH + NO2) = (8.95 +/- 2.70) x 10(-11) x (T/300 K)(-0.54 +/- 0.27) (T = 298-363 K), k(CH2CH2OH + NO2) = (5.99 +/- 1.80) X 10(-11) X (T/300 K)(-1.49 +/- 0.45) (T = 241-363 K), k(CH3CHOH + NO2) = (7.48 +/- 2.24) X 10(-11) X (T/300 K)(-136)+/- 0.41 (T = 266-363 K), k(CH3OCH2 + NO2) = (7.85 +/- 2.36) X 10(-11) X (T/300 K)(-0.93 +/- 0.28) (T = 243-363 K), and k(CH3CO + NO2) =(2.87 +/- 0.57) X 10(-11) X (T/300 K)(-2.45 +/- 0.49) (T = 241-363 K), where the uncertainties refer to the estimated overall uncertainties of the values obtained. The determined rate coefficients show negative temperature dependence with no apparent bath gas pressure dependence under the current experimental conditions (241-363 K and about 1-3 Torr helium). This behavior is typical for a radical-radical addition mechanism with no potential energy barrier above the energy of the separated reactants in the entrance channel of the reaction. Unfortunately the absence of detected product signals prevented gaining deeper insight into the reaction mechanism.