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Hydrogen, reaction with hydroxyl

The stability of perchlorofluoroalkanes is due to the absence of hydrogen atoms that may be abstracted by reaction with hydroxyl radicals. Attention has therefore been directed to chlorofluo-roalkanes containing at least one hydrogen atom (Hayman and Derwent 1997). Considerable effort has also been directed to the reactions of chloroalkanes and chloroalkenes, and this deserves a rather more detailed examination in the light of interest in the products that are formed. [Pg.18]

Nitric oxide is a physiological substrate for mammalian peroxidases [myeloperoxide (MPO), eosinophil peroxide, and lactoperoxide), which catalytically consume NO in the presence of hydrogen peroxide [60], On the other hand, NO does not affect the activity of xanthine oxidase while peroxynitrite inhibits it [61]. Nitric oxide suppresses the inactivation of CuZnSOD and NO synthase supposedly via the reaction with hydroxyl radicals [62,63]. On the other hand, SOD is able to modulate the nitrosation reactions of nitric oxide [64]. [Pg.699]

The surface of silica is highly reactive and hydroxyl groups exchange hydrogen for deuterium with D20 [14—16] but not with D2. They can be replaced by Cl from Cl2 or CC14 [16] and they react with silanes and aluminium chloride [15,19], Surface alcoholates are formed when silica is contacted with primary or secondary alcohols [20] either by the reaction with hydroxyl groups... [Pg.265]

The oxidation scheme for halomethanes not containing a hydrogen atom is similar to that for those which do, except that it is not initiated by tropospheric reaction with hydroxyl radicals, since the fully halogenated methanes are unreactive. Consequently, substantial amounts of CFCs and halons are transported intact up into the stratosphere, where they absorb UV radiation of short wavelength and undergo photodissociation (equation 36) to a halogen atom and a trihalomethyl radical. The halogen atom Y may enter into catalytic cycles for ozone destruction, as discussed in the introduction. [Pg.1566]

Fenton s original observation, made nearly 100 years ago, was that malic acid was rapidly oxidized by hydrogen peroxide when Fe(II) was added, but not otherwise (Fenton, 1894). Much later, Haber and Weiss (1934) suggested that such induced oxidations were due to reaction with hydroxyl radicals formed by reaction [4.7]. [Pg.104]

The problems of adhesion viewed from a chemical bonding standpoint are similar. Typical metal mold surfaces have been shown by Kaelble (7 ) to have a surface hydroxide layer of about (40-80) A. Such a surface provides two possible modes of chemical bonding, reaction of the ionic metal - hydroxide directly with the isocyanate, not too likely, or via hydrogen bonding with hydroxyl or other functions of either the chain extender and/or polyol. [Pg.205]

Isocyanates are very reactive toward compounds containing labile hydrogen atoms, forming addition compounds with the hydrogen donors. One such reaction, with hydroxyl-bearing compounds to form carbamates, or urethanes,... [Pg.285]

Wheland and Farr, 150), but their rates of reaction with hydroxyl ion are in the reverse order, so that the dependence of velocity upon acid strength is the exact opposite of that usually found. Moreover, the effect of alkyl substitution in increasing the acidity is the opposite of the usual inductive effect (e.g., in the carboxylic acids). It seems likely that the sequence of acid strengths results from the stabilization of the undissociated molecule by a hyperconjugative effect which depends on the number of hydrogen atoms on the carbon adjacent to the nitro group, e.g., in nitromethane we can write three structures of the type... [Pg.204]

The reaction of hydrogen ion with hydroxyl ion in water, called neutralization, is written... [Pg.150]

Kinetics of the reactions of hydrogen iodide with hydroxyl and nitrate radicals,... [Pg.271]

Polycondensation in the Presence of Polysaccharide. Polysaccharide was expected to play a role as a matrix in the polycondensation of hydroxyl diester with diamine, because hydroxyl groups in polysaccharide may have hydrogen bonding with hydroxyl diester. Therefore, the polycondensation of DMT with HMD was carried out in the presence of various sugars, such as dextrose, saccharose, 3-cyclodextrine(3-CD) and PF. The results shown in Figure 3 indicate that the polycondensation reaction in DMSO was greatly accelerated by the addition of these matrices in the following order ... [Pg.72]


See other pages where Hydrogen, reaction with hydroxyl is mentioned: [Pg.716]    [Pg.292]    [Pg.164]    [Pg.149]    [Pg.206]    [Pg.138]    [Pg.378]    [Pg.175]    [Pg.20]    [Pg.790]    [Pg.276]    [Pg.169]    [Pg.267]    [Pg.466]    [Pg.190]    [Pg.15]    [Pg.69]    [Pg.257]    [Pg.324]    [Pg.201]    [Pg.1566]    [Pg.694]    [Pg.855]    [Pg.295]    [Pg.425]    [Pg.1087]    [Pg.39]    [Pg.239]    [Pg.789]    [Pg.806]    [Pg.71]    [Pg.115]    [Pg.374]    [Pg.69]    [Pg.43]   


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Hydrogen hydroxylation

Hydrogen, reaction with hydroxyl radicals

Hydrogen, tropospheric reaction with hydroxyl

Hydrogenation reaction with

Hydroxyl radical with hydrogen peroxide, reaction

Hydroxyl, reactions

Hydroxylation reaction

Reaction with hydrogen

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