The IR absorbance of adsorbed CO is a suitable probe for evaluating the extent of oxidation of small supported copper particles. The residual absorbance of the main band at about 2120 cm^-1 after evacuation of the gas phase and the presence of additional CO absorbance bands indicate the extent of oxidation. Exposure of a reduced catalyst to NO brings about the oxidation of the copper particles. With increasing extent of oxidation the intensity of bands due to adsorbed NO and to adsorbed nitrito and nitrato like species increases. Adsorbed NO already desorbs upon room-temperature evacuation, the nitrito and nitrato like species decompose at temperatures between 423 and 473 K. The formation of N₂O (during exposure of NO to a catalyst which is not completely oxidized) and the formation of isocyanate (during subsequent exposure to CO) indicate the removal of weakly adsorbed nitrogen, originating from dissociated NO, from the surface of the copper particles. Upon simultaneous exposure of the reduced catalyst to equimolar amounts of NO and CO at room temperature, a surface reaction proceeds: the copper particles are not severely oxidized and the formation of CO₂, N₂O and isocyanate is observed. The agreement of the results from IR spectroscopy with those from XPS and anticipated from single-crystal results is good.