Halides decomposition

The hydrogen reduction of the metal halides, described in Sec. 1.2, is generally the favored reaction for metal deposition but is not suitable for the platinum-group metals since the volatilization and decomposition temperatures of their halides are too close to provide efficient vapor transport. 1 1 For that reason, the decomposition of the carbonyl halide is preferred. The exception is palladium which is much more readily deposited by hydrogen reduction than by the carbonyl-halide decomposition. 

Problem In order to study hydrogen halide decomposition, a researcher fills an evacuated... 

Dissociation of HI is the only exothermic process in the set of hydrogen halide decompositions ... 

Non-equilibrium plasma processes are much less sensitive to reverse reactions, because of low temperature, and often don t require product quenching. For this reason, several direct halide decomposition processes have been effectively carried out in non-thermal discharges. 

As it was pointed out, halide may contain the element to be nitrided in a number of cases. This fact laid the basis for obtaining refractory compositions from SHS-Az systems in which only one initial combustible element is present. The second one is formed because of halide decomposition which is contained in the same initial mixture. This is rather efficient both for economical reasons (for example, boron appears more effective in the formation of halide in initial mixtures) and... 

Problem In order to study hydrogen halide decomposition, a researcher fills an evacuated 2.00-L flask with 0.200 mol of HI gas and allows the reaction to proceed at 453°C ... 

Sheppard N and De La Cruz C 1998 Vibrational spectra of hydrocarbons adsorbed on metals. Part II. Adsorbed acyclic alkynes and alkanes, cyclic hydrocarbons including aromatics and surface hydrocarbon groups derived from the decomposition of alkyl halides, etc Adv. Catal. 42 181-313... 

The higher iodides, however, tend to be unstable and decomposition occurs to the lower iodide (PI5 -> PI3). Anhydrous chlorides and bromides of some metals may also be prepared by the action of acetyl (ethanoyl) halide on the hydrated ethanoate (acetate) in benzene, for example cobalt(II) and nickel(II) chlorides ... 

Gattermann (1890) found that the preparation of the cuprous halide may be avoided by making use of the fact that finely-divided copper (e.g., freshly-precipitated or reduced by hydrogen or copper bronze) acts catal3d.ically in the decomposition of solutions of diazonium salts, for example ... 

Uranium can be prepared by reducing uranium halides with alkali or alkaline earth metals or by reducing uranium oxides by calcium, aluminum, or carbon at high temperatures. The metal can also be produced by electrolysis of KUF5 or UF4, dissolved in a molten mixture of CaCl2 and NaCl. High-purity uranium can be prepared by the thermal decomposition of uranium halides on a hot filament. 

The majority of preparative methods which have been used for obtaining cyclopropane derivatives involve carbene addition to an olefmic bond, if acetylenes are used in the reaction, cyclopropenes are obtained. Heteroatom-substituted or vinyl cydopropanes come from alkenyl bromides or enol acetates (A. de Meijere, 1979 E. J. Corey, 1975 B E. Wenkert, 1970 A). The carbenes needed for cyclopropane syntheses can be obtained in situ by a-elimination of hydrogen halides with strong bases (R. Kdstcr, 1971 E.J. Corey, 1975 B), by copper catalyzed decomposition of diazo compounds (E. Wenkert, 1970 A S.D. Burke, 1979 N.J. Turro, 1966), or by reductive elimination of iodine from gem-diiodides (J. Nishimura, 1969 D. Wen-disch, 1971 J.M. Denis, 1972 H.E. Simmons, 1973 C. Girard, 1974),... 

Hafnium Halides. Hafnium tetrafluoride, HfF, can be prepared by careful thermal decomposition of ammonium fluorohafnate in an... 

Rhenium Halides and Halide Complexes. Rhenium reacts with chlorine at ca 600°C to produce rheniumpentachloride [39368-69-9], Re2Cl2Q, a volatile species that is dimeric via bridging hahde groups. Rhenium reacts with elemental bromine in a similar fashion, but the metal is unreactive toward iodine. The compounds ReCl, ReBr [36753-03-4], and Rel [59301-47-2] can be prepared by careful evaporation of a solution of HReO and HX. Substantiation in a modem laboratory would be desirable. Lower oxidation state hahdes (Re X ) are also prepared from the pentavalent or tetravalent compounds by thermal decomposition or chemical reduction. 

Molten halides are liquid electrolytes in many instances, and their decomposition may be canned out in principle to produce the metal and halogen, usually in the gaseous state. The theoretical decomposition voltage, E°, is calculated from the Gibbs energy of formation tlrrough the equation... 

Methylsuccinic acid has been prepared by the pyrolysis of tartaric acid from 1,2-dibromopropane or allyl halides by the action of potassium cyanide followed by hydrolysis by reduction of itaconic, citraconic, and mesaconic acids by hydrolysis of ketovalerolactonecarboxylic acid by decarboxylation of 1,1,2-propane tricarboxylic acid by oxidation of /3-methylcyclo-hexanone by fusion of gamboge with alkali by hydrog. nation and condensation of sodium lactate over nickel oxide from acetoacetic ester by successive alkylation with a methyl halide and a monohaloacetic ester by hydrolysis of oi-methyl-o -oxalosuccinic ester or a-methyl-a -acetosuccinic ester by action of hot, concentrated potassium hydroxide upon methyl-succinaldehyde dioxime from the ammonium salt of a-methyl-butyric acid by oxidation with. hydrogen peroxide from /9-methyllevulinic acid by oxidation with dilute nitric acid or hypobromite from /J-methyladipic acid and from the decomposition products of glyceric acid and pyruvic acid. The method described above is a modification of that of Higginbotham and Lapworth. ... 

Because a neutral molecule is eliminate4 rather than an anion, there is no electrostatic attraction (ion pairing) between the products of the dissociation step. As a result, the carbocations generated by diazonium-ion decomposition frequently exhibit somewhat different behavior from those generated from halides or sulfonates under solvolytic conditions. ... 

When halide ions or anions such as thiocyanate or azide are present, these anions are incorporated into the organic radical generated by decomposition of the peroxide. This anion transfer presumably occurs in the same step as the redox interaction with Cu(II), and such reactions have been called ligand-transfer reactions. " ... 

The Bergmann variation of the Balz Schiemann reaction is a two-step process featuring copper- or copper halide-catalyzed decomposition of aqueous or acetone solutions of arenediazonium fluoroborates containing alkyl or halogen substituents [30] A recent modification is a one-step technique featuring simultaneous diazoti-zation and decomposition by addition of aqueous sodium nitrite at 25 °C to a mixture of fluorobonc acid, copper powder, and 2 isopropyl 6 methylaniline to give 2-isopropyl-6 methylfluorobenzene in 73% yield [37]... 

The preparation of a tnflate salt may include the decomposition of tnflyl azide by azide ion Tnflyl azide can be prepared by the reaction of the azide ion with tnfluoromethanesulfonyl fluonde or tnfluoromethanesulfomc anhydnde [18] (equauonlS) Anotherone stepprocedureusesaquatemaryammoniumcountenon [J9] (equation 15) This tnflate can react with primary halides to form tn fluoromethyl sulfones [19 (equation 16) (Table 7)... 

An extension ot this reaction provides a number of other perfluorovinylic halides [54] The type of reaction products from the thermal decomposition reaction and the type of hydrocarbon Grignard reagent used in the exchange reaction are solvent-dependent When an excess ot phenylmagnesium bromide is used, a variety of phenylated products are formed depending on the excess amount used [4S (equation 23)... 

Monomeric thiazyl halides NSX (X = F, Cl Br) have been characterized in the gas phase, but oligomerization to cyclic species, e.g., (NSX)3 (X = F, Cl) and (NSF)4, occurs in the condensed phase (Section 8.7). These ligands can be stabilized, however, by coordination to a transition metal. The NSF complexes are conveniently prepared in SO2 (Eq. 1.6) The monomeric fluoride NSF is conveniently generated in situ by thermal decomposition of FC(0)NSF2 or Hg(NSp2)2 (Section 8.2). 

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