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Nitrogen dioxide intermediate

Cancelling the nitrogen dioxide intermediate and the nitrogen monoxide catalyst gives the overall reaction ... [Pg.567]

Efforts to raise the alpha-selectivity have been made. Thus nitration of anthraquinone using nitrogen dioxide and ozone has been reported (17). l-Amino-4-bromoanthraquinone-2-sulfonic acid (bromamine acid) [116-81 -4] (8) is the most important intermediate for manufacturing reactive and acid dyes. Bromamine acid is manufactured from l-aminoanthraquinone-2-sulfonic acid [83-62-5] (19) by bromination in aqueous medium (18—20), or in concentrated sulfuric acid (21). l-Aminoanthraquinone-2-sulfonic acid is prepared from l-aminoanthraquinone by sulfonation in an inert, high boiling point organic solvent (22), or in oleum with sodium sulfate (23). [Pg.310]

The reaction with nitrite proceeds smoothly and with relatively high yields of the corresponding nitroarene (see Sec. 10.6). Obviously a major part of the driving force of this reaction is the formation of a stable, i. e., an energetically favorable, radical, nitrogen dioxide. With the hydroxide ion — a much stronger nucleophile than the nitrite ion — the reaction is expected to produce very unstable radicals, the hydroxy radical OH and the oxygen radical anion O, from the diazohydroxide (Ar - N2 — OH) and the diazoate (Ar-N20 ) respectively. Consequently, dediazoniation in alkaline aqueous solution does not follow the simple Scheme 8-41 with Yn = OH, but instead involves diazoanhydrides (Ar — N2 —O —N2 —Ar) as intermediates (see Sec. 8.8). [Pg.195]

Peroxynitrite reacts with heme proteins such as prostacycline synthase (PGI2), microperoxidase, and the heme thiolate protein P450 to form a ferryl nitrogen dioxide complex as an intermediate [120]. Peroxynitrite also reacts with acetaldehyde with the rate constant of 680 1 mol 1 s" 1 forming a hypothetical adduct, which is decomposed into acetate, formate, and methyl radicals [121]. The oxidation of NADH and NADPH by peroxynitrite most certainly occurs by free radical mechanism [122,123], Kirsch and de Groot [122] concluded that peroxynitrite oxidized NADH by a one-electron transfer mechanism to form NAD and superoxide ... [Pg.704]

Much evidence has been accumulated that the ozone-olefin reaction has a predominant role in aerosol formation from alkenes, cyclic olefins, diolefins, and other unsaturated compounds. Free radicals are formed in the reaction and can react further, along with nitric oxide and nitrogen dioxide, either with the various intermediates or with the olefin itself (see the recent review by Pitts and Finlayson ). [Pg.72]

The gas-phase reactivity of various terpenes has been measured. Stephens and Scott were the first to include two terpenes (pinene and a-phel-landrene) with their study of the relative reactivity of various hydrocar ns. Both monoterpenes showed the high reactivity predicted by their olefinic structure. Conversion of nitric oxide to nitrogen dioxide in e presence of isoprene is at a rate intermediate between those for ethylene and trans-2-butene, and Japar et al, reported rate constants for the a-pinene and terpinolene-ozone reactions. Grimsrud et a/. measured the rate con-... [Pg.99]

Chemical radicals—such as hydroxyl, peroxyhydroxyl, and various alkyl and aryl species—have either been observed in laboratory studies or have been postulated as photochemical reaction intermediates. Atmospheric photochemical reactions also result in the formation of finely divided suspended particles (secondary aerosols), which create atmospheric haze. Their chemical content is enriched with sulfates (from sulfur dioxide), nitrates (from nitrogen dioxide, nitric oxide, and peroxyacylnitrates), ammonium (from ammonia), chloride (from sea salt), water, and oxygenated, sulfiirated, and nitrated organic compounds (from chemical combination of ozone and oxygen with hydrocarbon, sulfur oxide, and nitrogen oxide fragments). ... [Pg.239]

Kinetic characteristics are obtained for the reaction between several polycyclic aromatic hydrocarbons with nitrogen dioxide in dichloromethane at 25°C. They are in accord with the intermediate formation of the cation-radicals (Pryor et al 1984). [Pg.258]

Comparatively insoluble gases such as nitrogen dioxide and phosgene are not removed by the moisture in the upper respiratory tract and can easily reach the alveoli. Substances of intermediate solubility such as chlorine can cause irritation at points all along the respiratory tract. [Pg.6]

Nitrosylsulfuric acid is produced as an intermediate in the manufacture of sulfuric acid using the lead chamber process by the reaction of sulfur dioxide, nitrogen dioxide, oxygen, and water. [Pg.661]

The acid-base properties of fused alkali nitrates were first noted when dichromate was added to fused sodium-potassium nitrate eutectic (/)/. Gaseous nitrogen dioxide and oxygen were slowly given off with the conversion of the dichromate to chromate. It was postulated that N02+ was formed as intermediate ... [Pg.219]

The effect (upon the overall rate of conversion of dichromate to chromate) of changing the chromate ion concentration was studied. The rate was inversely proportional to the square of the chromate concentration, as well as proportional to the dichromate concentration. Since oxygen and nitrogen dioxide had no effect on the rate, the nitryl ion, N(>2+ was postulated as intermediate. However, the equilibrium constant for the reaction could not be determined because too little N02+ was formed. [Pg.219]

The very low value of Ashmore and Burnett is difficult to explain. It is easy to demonstrate that the discrepancy is not resolved by assuming the N03 intermediate in nitrogen dioxide decomposition is the pernitrite radical, in contradistinction to the symmetric nitrate radical. Their calculation of k5 depended on an experimentally obtained value for k 5 and an equilibrium constant K5- 5 calculated from thermodynamic properties for N03 measured by Schott and Davidson and Ray and Ogg. These results, obtained in a nitrogen pentoxide system, pertain to the nitrate radical, not the pernitrite radical. Guillory and Johnston176 reported an equilibrium constant based on estimated... [Pg.201]

Nitric oxide first reacts with atmospheric 02 to give nitrogen dioxide, a poisonous brown gas. Subsequently, N02 absorbs sunlight and dissociates to give an oxygen atom, which then reacts with 02 to form ozone. As usual, the catalyst (NO) and the intermediates (N02 and O) do not appear in the chemical equation for the overall reaction. [Pg.508]


See other pages where Nitrogen dioxide intermediate is mentioned: [Pg.278]    [Pg.458]    [Pg.424]    [Pg.119]    [Pg.374]    [Pg.55]    [Pg.6]    [Pg.130]    [Pg.242]    [Pg.235]    [Pg.237]    [Pg.950]    [Pg.954]    [Pg.962]    [Pg.963]    [Pg.21]    [Pg.39]    [Pg.289]    [Pg.252]    [Pg.261]    [Pg.212]    [Pg.296]    [Pg.642]    [Pg.648]    [Pg.45]    [Pg.46]    [Pg.50]    [Pg.50]    [Pg.50]    [Pg.200]    [Pg.131]    [Pg.41]    [Pg.4]    [Pg.380]    [Pg.145]   
See also in sourсe #XX -- [ Pg.454 , Pg.457 , Pg.458 , Pg.459 ]




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