Hydrogen iodide oxidation

For 2-amino-4- m-nitrophenyl) seienazole, the yield is particularly high. This has been explained by the oxidizing effect of the nitro group, which liberates iodine from the hydrogen iodide eliminated in the condensation reaction. 

Oxidation. Hydrogen peroxide is a strong oxidant. Most of its uses and those of its derivatives depend on this property. Hydrogen peroxide oxidizes a wide variety of organic and inorganic compounds, ranging from iodide ions to the various color bodies of unknown stmcture in ceUulosic fibers. The rate of these reactions may be quite slow or so fast that the reaction occurs on a reactive shock wave. The mechanisms of these reactions are varied and dependent on the reductive substrate, the reaction environment, and catalysis. Specific reactions are discussed in a number of general and other references (4,5,32—35). 

Complete iodination of organic compounds can be achieved by preventing the formation of free hydrogen iodide through the addition of an oxidizing agent, neutralization of the HI with a base, or combination using mercuric salts. 

Chemical Properties. The most significant chemical property of L-ascorbic acid is its reversible oxidation to dehydro-L-ascorbic acid. Dehydro-L-ascorbic acid has been prepared by uv irradiation and by oxidation with air and charcoal, halogens, ferric chloride, hydrogen peroxide, 2,6-dichlorophenolindophenol, neutral potassium permanganate, selenium oxide, and many other compounds. Dehydro-L-ascorbic acid has been reduced to L-ascorbic acid by hydrogen iodide, hydrogen sulfide, 1,4-dithiothreitol (l,4-dimercapto-2,3-butanediol), and the like (33). 

A variation of the general method for the synthesis of 2-amino-selenazoles is to avoid the use of the free a-halogenocarbonyl compound and in its place react the corresponding ketone and iodine with selenourea.This procedure is also taken from thiazole chemistry. By contrast with thiourea, the reaction with selenourea needs a longer reaction time and the work up of the reaction mixture is somewhat more difficult. Usually an excess of the ketone is used. In the preparation of 2-amino-4-( n-nitrophenyl)selenazole, a very high yield, calculated on the amount of iodine used, was obtained. To explain this peculiar result, the oxidative action of the nitro group was invoked. This liberates free iodine from some of the hydrogen iodide eliminated in the condensation reaction, and the free iodine then re-enters into the reaction. 

Heal content, 110. 116 change (luring a reaction, 110 of a substance, 109 Heat of combustion of diamond, 122 graphite, 122 hydrazine, 47 hydrogen, 40 methane, 123 Heat of formation, 113 Heat of reaction, 135 between elements, table, 112 oxidation of HC1, 160 oxidation of sulfur dioxide, 161 predicting, 112 Heat of reaction to form ammonia, 112 Br atoms, 290 carbon dioxide, 112 carbon monoxide, 112 Cl atoms, 290 CO + Hi, 110 ethane, 112 F atoms, 290 H atoms, 274 hydrogen chloride, 160 hydrogen iodide, 112 iron(Ill) oxide, 162 Li atoms, 290 Li + Br, 290 Li + F, 290 Na + Cl, 290 NHs products, 114 Na atoms, 290 NO, 112 NOj, 112... 

Alcohols react with nascent hydroiodic acid to form alkyl iodides. When the starting material is an alcohol ether sulfate, the resulting alcohol ethoxylate obtained by acid hydrolysis of the sulfate gives the corresponding alkyl iodides. The number of moles of diiodoethane equals the number of moles of ethylene oxide present in the alcohol ethoxylate. Diiodoethane decomposes or reacts with more hydrogen iodide to give iodine quantitatively in both cases. However,... 

The first reported porphyrin complexes of platinum(IV) date from 1980 and were obtained by hydrogen peroxide oxidation of platinum(II) porphyrin complexes in an acidic medium (HC1).479 Since then oxidation of platinum(II) complexes of other porphyrins has been achieved by the same method,480 and by chlorine,481 or bromine482 oxidation. Reaction with iodine did not lead to oxidation and treatment of platinum(IV) porphyrin complexes with iodide resulted in reduction to platinum(II). 

Write the formula for each of the following compounds (a) hydrogen iodide, (b) calcium chloride, (c) lithium oxide, (d) silver nitrate, (e) iron(II) sulfide, (/) aluminum chloride, (g) ammonium sulfate, (h) zinc carbonate, (/) iron(lll) oxide, ( ) sodium phosphate, (k) iron(H) acetate, (/) ammonium cyanide, and (m) copper(II) chloride. 

Similar acetic acid conversions and higher acid yield distributions using ruthenium(IV) oxide in combination with methyl iodide, ethyl iodide and hydrogen iodide as the added iodide promoter under comparable conditions. This is consistent with these different starting materials ultimately forming the same catalytically active species. 

Volatile decomposition products may include hydrogen chloride (HCl), hydrogen bromide (HBr), hydrogen iodide (HI), CO2, aromatic hydrocarbons, and nitrogen oxides (NO ). 

IDAS A process for making isoprene (for the manufacture of a synthetic rubber) by the oxidative dehydrogenation of isopentene. Iodine is the initial reactant the hydrogen iodide produced in the reaction is reconverted to elemental iodine via nickel iodide. 

From Eq. (a) step 1, it is obvious that the oxidation of sulphur dioxide takes place by iodine to yield sulphur trioxide and hydrogen iodide thereby consuming one mole of water. In other words, each one molecule... 

Reaction (9) generates methyl iodide for the oxidative addition, and reaction (10) converts the reductive elimination product acetyl iodide into the product and it regenerates hydrogen iodide. There are, however, a few distinct differences [2,9] between the two processes. The thermodynamics of the acetic anhydride formation are less favourable and the process is operated much closer to equilibrium. (Thus, before studying the catalysis of carbonylations and carboxylations it is always worthwhile to look up the thermodynamic data ) Under standard conditions the AG values are approximately ... 

Similar waves in the cathodic polarogram were observed by Donnet and Henrich 58) using oxidized carbon black. The wave disappeared after treatment with isobutyronitrile. It was assumed that isobutyro-nitrile gives an addition reaction with quinones. No reaction with this reagent was observed after reduction with hydrogen iodide, after treatment with aniline, or after treatment with diazomethane. The latter finding confirms the assumption by Studebaker et al. 38) that diazomethane is added to the quinones in the carbon black surface. 

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