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Manganese reaction with

Chemical ingenuity in using the properties of the elements and their compounds has allowed analyses to be carried out by processes analogous to the generation of hydrides. Osmium tetroxide is very volatile and can be formed easily by oxidation of osmium compounds. Some metals form volatile acetylacetonates (acac), such as iron, zinc, cobalt, chromium, and manganese (Figure 15.4). Iodides can be oxidized easily to iodine (another volatile element in itself), and carbonates or bicarbonates can be examined as COj after reaction with acid. [Pg.100]

Acidic Properties. As a typical acid, it reacts readily with alkaUes, basic oxides, and carbonates to form salts. The largest iadustrial appHcation of nitric acid is the reaction with ammonia to produce ammonium nitrate. However, because of its oxidising nature, nitric acid does not always behave as a typical acid. Bases having metallic radicals ia a reduced state (eg, ferrous and staimous hydroxide becoming ferric and stannic salts) are oxidized by nitric acid. Except for magnesium and manganese ia very dilute acid, nitric acid does not Hberate hydrogen upon reaction with metals. [Pg.39]

Sihca is reduced to siUcon at 1300—1400°C by hydrogen, carbon, and a variety of metallic elements. Gaseous siUcon monoxide is also formed. At pressures of >40 MPa (400 atm), in the presence of aluminum and aluminum haUdes, siUca can be converted to silane in high yields by reaction with hydrogen (15). SiUcon itself is not hydrogenated under these conditions. The formation of siUcon by reduction of siUca with carbon is important in the technical preparation of the element and its alloys and in the preparation of siUcon carbide in the electric furnace. Reduction with lithium and sodium occurs at 200—250°C, with the formation of metal oxide and siUcate. At 800—900°C, siUca is reduced by calcium, magnesium, and aluminum. Other metals reported to reduce siUca to the element include manganese, iron, niobium, uranium, lanthanum, cerium, and neodymium (16). [Pg.471]

Alkyds. Alkyd resins (qv) are polyesters formed by the reaction of polybasic acids, unsaturated fatty acids, and polyhydric alcohols (see Alcohols, POLYHYDRic). Modified alkyds are made when epoxy, sUicone, urethane, or vinyl resins take part in this reaction. The resins cross-link by reaction with oxygen in the air, and carboxylate salts of cobalt, chromium, manganese, zinc, or zirconium are included in the formulation to catalyze drying. [Pg.365]

Chemical Properties. Potassium cyanide is readily oxidized to potassium cyanate [590-28-3] by heating in the presence of oxygen or easily reduced oxides, such as those of lead or tin or manganese dioxide, and in aqueous solution by reaction with hypochlorites or hydrogen peroxide. [Pg.385]

N- Aminoaziridines have been converted to alkenes by reaction with a variety of oxidizing agents (70JA1784). Usually, the deamination reaction is stereospecific. The oxidation of l-amino-2,3-diphenylaziridines with manganese dioxide, however, was not stereospecific. The trans compound gives entirely frans-stilbene, whereas the cfs-aziridine forms a mixture of 85% trans- and 15% c -aikene. cw-Stilbene is not isomerized to trans under the reaction conditions, and the results are explained in terms of an azamine intermediate which can isomerize through a tautomeric equilibrium. [Pg.74]

Metal ions in their reduced state also undergo reactions with BrCl. Examples include iron and manganese. [Pg.479]

Desimoni et al. have found that chiral BOX-manganese(II) complexes can catalyze the intramolecular cycloaddition and ene reactions, with the latter as the major product [37]. [Pg.170]

In order to avoid loss of oxygen from the water sample it is fixed by its reaction with manganese)II) hydroxide which is converted rapidly and quantitatively to manganese)III) hydroxide ... [Pg.395]

This photodriven benzannulation was used in the synthesis of indolocar-bazoles (Eq. 22) [96] and calphostins (Eq. 23) [97]. The thermal insertion of isonitriles into these same classes of carbenes provided a complementary approach to similar benzannulations [98-100]. Manganese alkoxycarbene complexes underwent both inter- [101] and intramolecular [102] photodriven benzannulation reactions with alkynes (Eqs. 24 and 25). [Pg.181]

There is a paucity of information on reactions of the strongly-oxidising manganese(lll) with inorganic substrates. The main reason for this neglect lies in the tendency of Mn(lII) to disproportionate, viz. [Pg.172]

Wallington TJ, O Sokolov, MD Hurley, GS Tyndall, 11 Orlando, 1 Barnes, KH Becker, R Vogt (1999) Atmospberic cbemistry of metbylcyclopentadienyl manganese tricarbonyl photolysis, reaction with bydroxyl radicals and ozone. Environ Sci Technol 33 4232-4238. [Pg.48]

Another example for reactions with the insertion of protons is the cathodic reduction of manganese dioxide, which occnrs dnring discharge of the positive electrodes in zinc-manganese dioxide batteries. This reaction can be formulated as... [Pg.443]

Zinc gives an explosive reaction with manganese dichloride, whereas with calcium chloride, which was in a galvanised iron container, the detonation is blamed on the overpressure created by the release of hydrogen, which is formed in these conditions. [Pg.209]


See other pages where Manganese reaction with is mentioned: [Pg.514]    [Pg.386]    [Pg.514]    [Pg.386]    [Pg.254]    [Pg.279]    [Pg.283]    [Pg.126]    [Pg.671]    [Pg.55]    [Pg.707]    [Pg.551]    [Pg.167]    [Pg.585]    [Pg.299]    [Pg.141]    [Pg.292]    [Pg.1025]    [Pg.283]    [Pg.86]    [Pg.314]    [Pg.47]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.498 ]




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Alcohols, reaction with manganese dioxide

Azides, reaction with manganese

Germanium—manganese bonds reactions with

Hydrochloric acid reaction with manganese dioxide

Lead—manganese bonds reactions with

Manganese acetate reaction with alkenes

Manganese acetate, reaction with aldehydes

Manganese carbyne, reactions with

Manganese compounds, crotyltype III reactions with aldehydes

Manganese decacarbonyl, reaction with

Manganese diazo compounds, reactions with

Manganese dioxide reaction with saturated alcohols

Manganese dioxide, reaction with

Manganese dioxide, reaction with potassium chlorate

Manganese oxides reactions with metals

Manganese reaction

Manganese thiophene, reactions with

Manganese—silicon bonds reactions with

Potassium chlorate reaction with manganese oxide

Reaction with manganese acetate

With manganese

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