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Subject carbon oxides

When an aromatic compound having an aliphatic side chain is subjected to oxidation, fission of the side chain occurs between the first and second carbon atoms from the benzene ring, the first carbon atom thus becoming part of a carboxyl ( -COOH) group. For example ... [Pg.239]

The reactions of olefins with peracids to form epoxides allows for the selective oxidation of carbon-carbon double bonds in the presence of other functional groups which may be subject to oxidation (for example, hydroxyl groups). The epoxides that result are easily cleaved by strong acids to diols or half-esters of diols and are therefore useful intermediates in the synthesis of polyfunctional compounds. [Pg.8]

The major androgen or androgen precursor produced by the adrenal cortex is dehydroepiandrosterone (DHEA). Most 17-hydroxypregnenolone follows the glucocorticoid pathway, but a small fraction is subjected to oxidative fission and removal of the two-carbon side chain through the action of 17,20-lyase. The lyase activity is actually part of the same enzyme (P450cl7) that catalyzes 17tt-hydroxylation. This is therefore a dual function protein. The lyase activity is important in both the adrenals and... [Pg.440]

Oxidative attack on a carbon-hydrogen bond of an alkyl group a to a nitrogen atom is not restricted to saturated aliphatic amines. In fact X in an X-N-CH- structural subunit can be virtually any common atomic grouping that can be found in stable organic molecules. For example, w-carbon hydrogens of Aralkyl-substituted aromatic cyclic amines (119), aryl amines (120), amides (121), amidines (122), A-nitrosodialkylamines (123), etc. are all subject to oxidative attack, carbinolamine formation, and in most cases release of an aldehyde or ketone depending on the substitution pattern (1° or 2°)... [Pg.79]

Combustion of transition metal organometallic compounds produces a mixtures of simple compounds (metal oxides, carbon oxides, water, nitrogen) which is subject to exact analysis. Thermal decomposition or high temperature iodination of the same compounds cannot necessarily be expected to produce simple materials, with the result that identification is often a difficult problem. This is typified by diene derivatives of iron carbonyl10, where side reactions of the dienes (e.g. polymerization) follow disruption of the iron-diene bonds. The oligomeric mixture can be parti-... [Pg.77]

Dwell time, or the time the molecule was actually in the lamp unit, and concentration were two parameters that affected the rate of degradation. Mass spectra of the trimethylsilyl (TMS) derivatives of atrazine subjected to UV-ozonation revealed a number of dehalogenated, dealkylated s -triazines, paraquat yielded the 4-picolinic acid, and 2,4-D gave oxalic acid, glycolic acid and several four-carbon oxidation products. The economics of UV-ozonation as a pretreatment for land disposal compares favorably with incineration and other options open to the small pesticide user. [Pg.195]

Such correlations have important bearings on the current level of understanding regarding the mechanisms of pyrolysis devolatilisation and char formation. Furthermore, standard forms of analyses are subject to oxidation or weathering effects and this study demonstrates that correlations between levels of unbumt carbon and vitrinite reflectance (33) maybe potentially misleading unless the affects of oxidation or weathering are considered. [Pg.297]

The purpose of the present paper is to offer a contribute to the understanding of the mechanisms of these reactions by using an IR spectroscopic method and well-characterized "monolayer" type vanadia-titania (anatase) as the catalyst. We will focus our paper in particular on the following subjects i) the nature of the activation step of the methyl-aromatic hydrocarbon ii) the mechanism of formation of maleic anhydride as a by-product of o-xylene synthesis iii) the main routes of formation of carbon oxides upon methyl-aromatic oxidation and ammoxidation iv) the nature of the first N-containing intermediates in the ammoxidation routes. [Pg.169]

Kotzick, R., U. Panne, and R. Niessner, Changes in Condensation Properties of Ultrafine Carbon Particles Subjected to Oxidation by Ozone, J. Aerosol Sci, 28, 725-735 (1997). [Pg.836]

The 2-(0-nitrobenzenesulfonamido)alcohol 359 was obtained from 358 through a sequence of reactions, which was then subjected to oxidation with Dess-Martin periodinane to give the 2-(t>-nitrobenzenesulfonamido)ketone 360 in 84% yield (Scheme 74). Upon reductive cyclization with hydrogen and palladium over activated carbon, 360 gave the 1,2,5-benzothiazepine 361 <2004T3349>. [Pg.472]

For the family of carbons similar in nature, the strong value increases with the specific surface area (S) but decreases to reach the value far lower than 0.5 9 when the support is subjected to oxidation [54—57,111,135]. For example, the strong value falls down linearly with increasing number of oxygen-containing groups [57]. The above speculations can be expressed in the simplest form as follows ... [Pg.455]


See other pages where Subject carbon oxides is mentioned: [Pg.47]    [Pg.33]    [Pg.8]    [Pg.741]    [Pg.53]    [Pg.548]    [Pg.299]    [Pg.140]    [Pg.243]    [Pg.43]    [Pg.130]    [Pg.151]    [Pg.369]    [Pg.444]    [Pg.600]    [Pg.1082]    [Pg.140]    [Pg.85]    [Pg.167]    [Pg.40]    [Pg.54]    [Pg.274]    [Pg.355]    [Pg.204]    [Pg.77]    [Pg.1]    [Pg.111]    [Pg.5973]    [Pg.291]    [Pg.211]    [Pg.847]    [Pg.191]    [Pg.92]    [Pg.301]    [Pg.337]    [Pg.355]    [Pg.302]    [Pg.96]    [Pg.382]   
See also in sourсe #XX -- [ Pg.2 , Pg.4 , Pg.5 , Pg.7 , Pg.8 , Pg.9 , Pg.63 ]




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Carbon Subject

Carbonate Subject

Subject Oxides

Subject oxidation

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