Peroxonitrate

Peroxonitrous acid, HOONO. Isomer of nitric acid (HNO2 plus H2O2). [Pg.279]

HNO4 peroxonitric acid H2S2O4 dithionous acid... [Pg.221]

HOONO peroxonitrous acid H2Se04 selenic acid... [Pg.221]

Peroxonitrous Acid and Its Salts. Peroxonitrous acid [14691-52-2] YLOON014691-52-2 is an isomer of nitric acid, HNO, to which it... [Pg.93]

Peroxonitrous acid can decompose by two pathways isomerization to nitric acid, and dissociation into the hydroxyl radical and nitrogen dioxide. [Pg.93]

The hydroxyl radical is responsible for some of the oxidation products of organic compounds by peroxonitrous acid. [Pg.93]

Peroxonitrite is beHeved to be present in the crystals of nitric acid trihydrate that form in the stratosphere and in Martian soil (see Extraterrestrial materials). Peroxonitrous acid may be present in mammalian blood and other biochemical systems. However, peroxonitric acid, HNO, is not known. Before the chemistry of peroxonitrous acid was understood, these two acids were sometimes confused. [Pg.93]

HOONO Peroxonitrous acid Unstable, isomeric with nitric acid some salts are more stable ... [Pg.459]

HNO4 Peroxonitric acid Unstable, explosive crystals, HOONO2 no solid salts known. (For orthonitrates , N04 , i.e. salts of the unknown orthonitric acid H3NO4, see p. 471 -2)... [Pg.459]

Peroxonitric Acid, HN04 Pure material decomposes. explosively at —30°. Solns in w or acet ac over 70% HNO4 decompose autocatalytically to ex pin R. Schwarz, ZAnorgChem 256, 3(1948)... [Pg.673]

Contact of cycloalkenes with a mixture of dinitrogen tetraoxide and excess oxygen at temperatures of 0°C or below produces nitroperoxonitrates of the general formula-CHN02-CH(OON02)—which appear to be unstable at temperatures above 0°C, owing to the presence of the peroxonitrate group. [Pg.1793]

Peroxomonosulfuric acid, 18 404—405 Peroxonitrite ion, 18 402 Peroxonitrous acid/salts, 18 402 Peroxophosphoric acids/salts, 18 402-404 Peroxopolyoxometallates, 18 415-416 Peroxosilicates, 18 402 Peroxosulfuric acids/salts, 18 404-405 Peroxotin compounds, 18 402 Peroxyacetic acid, 1 148 14 66, 67 Peroxyacetyl nitrate (PAN), 1 789, 795 Peroxyacids, 18 462 466... [Pg.685]

NITROALKYL PEROXONITRATES, NITROARYL COMPOUNDS NITROARYLPHOSPHINIC ACIDS, NITROBENZYL COMPOUNDS C-NITRO COMPOUNDS, A-NITRO COMPOUNDS ac/ -NITROQUINONOID COMPOUNDS, aci-NITRO SALTS POLYNITROALKYL COMPOUNDS, POLYNITROARYL COMPOUNDS POLYNITROAZOPYRIDINES Other relevant entries are ... [Pg.276]

Peroxodisulfuric acid, 4482 Peroxomonophosphoric acid, 4506 Peroxomonosulfuric acid, 4481 Peroxonitric acid, 4437... [Pg.331]

Trifluoromethyl 3-fluorocarbonylhexafluoroperoxybutyrate, 2061 Trifluoromethyl peroxonitrate, 0346 Trifluoromethyl peroxyacetate, 1103... [Pg.336]

Amels, P., Elias, H., Gotz, U., Steingens, U.. and Wannowius, K.J. Kinetic investigation ofthe stability of peroxonitric acid and... [Pg.1624]

Peroxonitrous Acid and Its Salts. Pcroxonitrous acid HOONO, is an isomer of nitric acid. HNOj, to which it rapidly converts. The half-life of peroxonitrous acid at 0 C is 10 s at 27°C, 0.23 s. It has been known since 1904 that the yellow solution made by mixing nitrous acid and hydrogen peroxide at low temperature contains a stronger oxidant than either ingredient alone, but the chemistry involved was not put on a sound basis until 1994. Additional preparatory methods are also available. [Pg.1228]

Peroxodisulfuric acid, 4476 Peroxomonophosphoric acid, 4501 Peroxomonosulfuric acid, 4475 Peroxonitric acid, 4431 Peroxyacetyl perchlorate, 0733 Peroxybenzoic acid, 2729... [Pg.2123]

NITROALKYL PEROXONITRATES NITROAROMATIC—ALKALI HAZARDS NITROARYL COMPOUNDS NITROARYLPHOSPHINIC ACIDS NITROBENZYL COMPOUNDS POLYNITROALKYL COMPOUNDS POLYNITROARYL COMPOUNDS POLYNITROAZOPYRIDINES... [Pg.2470]

Butyryl peroxonitrate, 1569 Di-ferf-butyl diperoxycarbonate, 3188 Di-ferf-butyl diperoxyphthalate, 3709... [Pg.2530]

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