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M oxidation

Although essentially inert m acid-base reactions alkanes do participate m oxidation-reduction reactions as the compound that undergoes oxidation Burning m air (combus tion) IS the best known and most important example Combustion of hydrocarbons is exothermic and gives carbon dioxide and water as the products... [Pg.83]

Oxidation of carbon corresponds to an increase in the number of bonds between carbon and oxygen or to a decrease in the number of carbon-hydrogen bonds Conversely reduction corresponds to an increase in the number of carbon-hydrogen bonds or to a decrease in the number of carbon-oxygen bonds From Table 2 4 it can be seen that each successive increase m oxidation state increases the number of bonds between carbon and oxygen and decreases the number of carbon-hydrogen bonds Methane has four C—H bonds and no C—O bonds car bon dioxide has four C—O bonds and no C—H bonds... [Pg.87]

Most of the time we are concerned only with whether a particular reaction is an oxidation or reduction rather than with determining the precise change m oxidation num ber In general Oxidation of carbon occurs when a bond between carbon and an atom that IS less electronegative than carbon is replaced by a bond to an atom that is more electronegative than carbon The reverse process is reduction... [Pg.88]

Particle thickness, p.m Oxide content, vol % Particle thickness, p.m Oxide content, vol %... [Pg.180]

Variety and source Si02 (siHca ) FeO (ferrou s oxide) 3 (ferri c oxide ) AI2O3 (alumina) MgO (magnesia) CaO (lime ) MnO (manganese oxide) Na20 (sodiu m oxide) icp (potassiu m oxide) up, adsoibe d up+, combine d... [Pg.346]

Kisamori, S., Kuroda, K., Kawano, S., Moehida, 1., Matsumura, Y. and Yoshikawa, M., Oxidative removal of SO2 and recovery of H2SO4 over poly(acrylonitrile)-baacd active carbon fiber. Energy Fuels, 1994, 8(6), 1337 1340. [Pg.115]

Electrochemical oxidation of alkyl aryl ethers results m oxidative dealkylation and coupling of the intermediate radicals ElectrooxidaUon m the presence of hydrogen fluonde salt leads to fluonnated dienones [66] (equation 58)... [Pg.341]

Oxyd-chlorid, n. oxychloride, -einschluss, m. oxide inclusion, -faden, m. Elec.) oxide-coated filament, -firms, m. oxide varnish (thickened drying oil). [Pg.330]

Latimer, W. M., Oxidation Materials, Prentice Hall, New Jersey (1952)... [Pg.113]

A piece of burning magnesium acts as a fuse when Inserted into a pot containing a finely divided mixture of aluminum powder and iron(m) oxide. [Pg.210]

Many nitroquinoxalines have been prepared by primary synthesis (see Chapter 1), from halogeno quinoxalines (see Section 3.2.7), or by passenger introduction (e.g., on deoxidative alkylation of an M-oxide see Section 4.6.2.2). However, one major route and one minor preparative route remain, and they are illustrated in the following subsections. [Pg.255]

For lists of some of the oxidizing agents used, with references, see Hudlicky, M. Oxidations in Organic Chemistry American Chemical Society Washington, 1990, p. 174 Ref. 92, p. 838 Srivastava, R.G. Venkataramani, P.S. Synth. Commun., 1988, 18, 2193. See also Haines, A.H. Ref. 207. [Pg.955]

Wefers, K. Bell, G. M. "Oxides and Hydroxides of Aluminum" Technical Paper No. 19 Alcoa Research Laboratories East St. Louis, 1972. [Pg.462]

Preparative-scale fermentation of papaveraldine, the known benzyliso-quinoline alkaloid, with Mucor ramannianus 1839 (sih) has resulted in a stereoselective reduction of the ketone group and the isolation of S-papaverinol and S-papaverinol M-oxide [56]. The structure elucidations of both metabolites were reported to be based primarily on ID and 2D NMR analyses and chemical transformations [56]. The absolute configuration of S-papaverinol has been determined using Horeau s method of asymmetric esterification [56]. The structures of the compounds are shown in Fig. 7. [Pg.116]

Hasegawa et al. have studied the photoreaction of benzofuroxan obtaining, hke in other M-oxide photochemistry, lactames [71-73]. [Pg.274]

Fukuzawa, K. Gebicki, J. M. Oxidation of alpha-tocopherol in micelles and liposomes by the hydroxyl, perhydroxyl, and superoxide free radicals. Arch. Biochem. Biophys. 1983, 226, 242-251. [Pg.212]

Skinner, W. A. Parkhurst, R. M. Oxidation products of vitamin E and its model, 6-hydroxy-... [Pg.214]


See other pages where M oxidation is mentioned: [Pg.393]    [Pg.708]    [Pg.781]    [Pg.862]    [Pg.115]    [Pg.208]    [Pg.113]    [Pg.30]    [Pg.330]    [Pg.380]    [Pg.998]    [Pg.998]    [Pg.998]    [Pg.998]    [Pg.998]    [Pg.521]    [Pg.692]    [Pg.99]    [Pg.1480]    [Pg.1569]    [Pg.260]    [Pg.266]    [Pg.154]    [Pg.492]    [Pg.320]    [Pg.126]    [Pg.278]    [Pg.288]    [Pg.541]   
See also in sourсe #XX -- [ Pg.279 ]




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Bobbitt, J. M., Periodate Oxidation

M-xylene oxidation

Oxidants m-CPBA

Oxidations m-chloroperbenzoic acid

Oxidative addition at M center

P-M oxidation

Perbenzoic acid, m-chloroBaeyer-Villiger reaction oxidation

Perbenzoic acid, m-chloroBaeyer-Villiger reaction oxidative halogenation

Pyridine-M-oxides

Shirwaiker, G. S., Bhatt, M. V., Chemistry Arene Oxides

The Iron Oxides: Structure, Properties, Reactions, Occurences and Uses. R. M. Cornell, U. Schwertmann

The Stabilization of Oxidation States R. S. Nyholm and M. L. Tobe

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