Abstract γ-Radiolysis of N2O-saturated water or photolysis of aqueous H2O2 provided a source of OH radicals. These radicals react with ethanol by preferentially abstracting an H atom at C-1. In the presence of oxygen these radicals are converted into the corresponding peroxyl radicals.The a-hydroxyethylperoxyl radicals decay by first order kinetic(k=k1 + k2 [OH-]) acetaldehyde and HO2˙/H+ + O2 ⨪ being the products (k1 (20 °C) = 50 ± 10 s-1 , Ea = 66 ± 7 kJ·mol-1 , k2= (4± 1) X 109 M-1 s-1). In competition (favoured by low pH, low temperature and high dose rate) they also decay by second order kinetics (2k3 = (7 ± 2) x 108 M-1 s-1). The most important route in the bimolecular decay leads to acetaldehyde, acetic acid and oxygen (ca. 75%). This route might largely be concerted (Russell mechanism), but there might also be a contribution from the disproportionation of oxyl radicals within the solvent cage. There is also a concerted route that leads to two molecules of acetic acid and to hydrogen peroxide (ca. 10%). Another pathway (ca. 15%) yields two oxyl radicals and oxygen. The former may either decompose into formic acid and methyl radicals (ca. 5%) or rearrange into 1,1-dihydroxyethyl radicals (ca. 10%). These radicals add oxygen and the resulting peroxyl radicals rapidly decompose into acetic acid and HO2˙. The reaction of a-hydroxyethylperoxyl radicals with HO2˙/O2⨪ radicals appears to be slow (k≈107 M-1s-1).
Product study and mechanisms of the reactions of α-pinene and of pinonaldehyde with OH radicals