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Retention oxidation

A similar intermediate is proposed to explain the retentive oxidation of Si-H bonds with perbenzoic acid. In this reaction, Br is replaced with OH and Cl is replaced with C6H5C02. Cleavage of alkyl groups from silicon can be accomplished with strongly electrophilic reagents, such as hydrogen halides in the presence of aluminum halides ... [Pg.23]

Formation of a Tr-allylpalladium complex 29 takes place by the oxidative addition of allylic compounds, typically allylic esters, to Pd(0). The rr-allylpal-ladium complex is a resonance form of ir-allylpalladium and a coordinated tt-bond. TT-Allylpalladium complex formation involves inversion of stereochemistry, and the attack of the soft carbon nucleophile on the 7r-allylpalladium complex is also inversion, resulting in overall retention of the stereochemistry. On the other hand, the attack of hard carbon nucleophiles is retention, and hence Overall inversion takes place by the reaction of the hard carbon nucleophiles. [Pg.15]

Furthermore, the catalytic allylation of malonate with optically active (S)-( )-3-acetoxy-l-phenyl-1-butene (4) yields the (S)-( )-malonates 7 and 8 in a ratio of 92 8. Thus overall retention is observed in the catalytic reaction[23]. The intermediate complex 6 is formed by inversion. Then in the catalytic reaction of (5 )-(Z)-3-acetoxy-l-phenyl-l-butene (9) with malonate, the oxidative addition generates the complex 10, which has the sterically disfavored anti form. Then the n-a ir rearrangement (rotation) of the complex 10 moves the Pd from front to the rear side to give the favored syn complex 6, which has the same configuration as that from the (5 )-( )-acetate 4. Finally the (S)-( )-mal-onates 7 and 8 are obtained in a ratio of 90 10. Thus the reaction of (Z)-acetate 9 proceeds by inversion, n-a-ir rearrangement and inversion of configuration accompanied by Z to isomerization[24]. [Pg.293]

The amount of herbicide sorbed by a given soil is influenced by properties of both the soil and the herbicide. Important properties related to the soil s retention abiHty include clay mineralogy, organic matter content, soil pH, and iron and aluminum oxide content. These properties, in turn, affect the... [Pg.47]

Oxidation. The oxidation reactions of organoboranes have been reviewed (5,7,215). Hydroboration—oxidation is an anti-Markovnikov cis-hydration of carbon—carbon multiple bonds. The standard oxidation procedure employs 30% hydrogen peroxide and 3 M sodium hydroxide. The reaction proceeds with retention of configuration (216). [Pg.314]

Aldehydes are important products at all pressures, but at low pressures, acids are not. Carbon monoxide is an important low pressure product and declines with increasing pressure as acids increase. This is evidence for competition between reaction sequence 18—20 and reaction 21. Increasing pressure favors retention of the parent carbon skeleton, in concordance with the reversibiUty of reaction 2. Propylene becomes an insignificant product as the pressure is increased and the temperature is lowered. Both acetone and isopropyl alcohol initially increase as pressure is raised, but acetone passes through a maximum. This increase in the alcohoLcarbonyl ratio is similar to the response of the methanoLformaldehyde ratio when pressure is increased in methane oxidation. [Pg.341]

Basic oxides of metals such as Co, Mn, Fe, and Cu catalyze the decomposition of chlorate by lowering the decomposition temperature. Consequendy, less fuel is needed and the reaction continues at a lower temperature. Cobalt metal, which forms the basic oxide in situ, lowers the decomposition of pure sodium chlorate from 478 to 280°C while serving as fuel (6,7). Composition of a cobalt-fueled system, compared with an iron-fueled system, is 90 wt % NaClO, 4 wt % Co, and 6 wt % glass fiber vs 86% NaClO, 4% Fe, 6% glass fiber, and 4% BaO. Initiation of the former is at 270°C, compared to 370°C for the iron-fueled candle. Cobalt hydroxide produces a more pronounced lowering of the decomposition temperature than the metal alone, although the water produced by decomposition of the hydroxide to form the oxide is thought to increase chlorine contaminate levels. Alkaline earths and transition-metal ferrates also have catalytic activity and improve chlorine retention (8). [Pg.485]

Sihcon nitride has good strength retention at high temperature and is the most oxidation resistant nitride. Boron nitride [10043-11 -5] has excellent thermal shock resistance and is in many ways similar to graphite, except that it is not an electrical conductor. [Pg.27]

Plasticity Retention Index. The oxidation behavior of natural mbber may affect both the processing characteristics and final vulcanizate performance, and the plasticity retention index (PRI) test can be used to give an indication of both. Natural antioxidants present in natural mbber give some protection and a measure of the efficacy of protection is given by PRI. PRI% = P q j Pq x 100, where Pq is the initial Wallace plasticity and P q is the... [Pg.269]

Mineralocorticoids. Aldosterone [6251-69-0] (32), the most potent natural rnineralocorticoid, also possesses a A -3-one group, an oxygen substituent at Clip, and a C17P-2-hydroxyethan-l-one side chain. In addition, the C18 of aldosterone is oxidized to an aldehyde. Mineralocorticoids, particularly aldosterone, act to retain sodium and to prevent the retention of excess potassium. Antimineral ocorticoids have been used therapeutically as diuretics and as agents that regulate blood pressure (63—65). [Pg.418]

Solutions of these fire retardant formulations are impregnated into wood under fliU cell pressure treatment to obtain dry chemical retentions of 65 to 95 kg/m this type of treatment greatly reduces flame-spread and afterglow. These effects are the result of changed thermal decomposition reactions that favor production of carbon dioxide and water (vapor) as opposed to more flammable components (55). Char oxidation (glowing or smoldering) is also inhibited. [Pg.329]


See other pages where Retention oxidation is mentioned: [Pg.327]    [Pg.327]    [Pg.130]    [Pg.136]    [Pg.319]    [Pg.65]    [Pg.254]    [Pg.319]    [Pg.319]    [Pg.275]    [Pg.475]    [Pg.489]    [Pg.34]    [Pg.36]    [Pg.409]    [Pg.33]    [Pg.11]    [Pg.62]    [Pg.72]    [Pg.164]    [Pg.322]    [Pg.471]    [Pg.178]    [Pg.181]    [Pg.321]    [Pg.344]    [Pg.35]    [Pg.279]    [Pg.559]    [Pg.256]    [Pg.65]    [Pg.109]    [Pg.19]    [Pg.400]    [Pg.421]    [Pg.421]    [Pg.11]   
See also in sourсe #XX -- [ Pg.10 , Pg.31 , Pg.32 , Pg.207 , Pg.209 , Pg.239 ]




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Retention Baeyer-Villiger oxidations

Retention oxidation of benzylic

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