with the mentioned sulfur compounds were determined at 3.7, 2.8, 13.0, 0.9 and 1.8 χ 10 16 cm 3 s _1 respectivelly. We also noticed the formation of a standard compound, which is considered to be of the type R-SNO.The irradiations of the hydrocarbons -the main part of this study -were studied in two smog chambers, one glass and one of teflon film, because due to the different absorbsnce characteristics of the two materials, completely different chemistry was expected to take place.By varying the hydrocarbon concentration under constant N0 2 concetration at 100 ppb, in both chambers, it is shown that η-butane and toluene have the lowest forming potential for ozone at all levels of the ratio HC/NO x , while olefins are particularly reactive and form the greatest amounts of ozone at low levels of the ratio HC/NO x . We point out that the rate of the reaction of hydrocarbons with the hydroxyl radicals is not, in all cases, a criterion for the ozone that can be formed. Thus, t-2-butene seems to be less reactive than expected on the base of the rate of its reaction with OH, since the internal double bond of the molecule reacts with ozone and consequently the latter is not only formed but destroyed as well. Propylene is a particular case, because as it has intermediate reactivity with both the hydrxyl radicals and ozone, it finally favours the formation of ozone. Concerning the formation of PAN we found out that the potential of the five hydrocarbons is of the following order : t-2-butene > propylene > toluene > aethene > η-butane. The latter, because of its slow reaction with hydroxyl radicals, forms the lowest amount of PAN, aethen is, as mentioned before, a special case while olefins form the highest amounts of PAN and, because of its chemical structure t-2-butene forms twice the quantity formed by propylene. Toluene is forming PAN in higher than the expected amounts, probably due to the the formation of predominant for PAN compounds, diacetyl and methyl glyoxal, formed by aromatic species.At the second section of the irradiations in the teflon chamber, under increasing concentration of N0 2 and constant concentration of the hydrocarbon, we noticed an increase in the formation of ozone formed as the N0 2 concentration increased, until the point of deactivation of the system. The fact that the maximums of ozone were determined at longer times than those of our previous experiments, is something which we expected because of the reaction of ozone with the NO formed. As far as PAN is concerned, we noticed a decrease at its maximum as the N0 2 levels increase,