Hydrogen chloride, hydration

Hydrogen chloride absorption, 12 746 Hydrogen chloride hydrates, 13 813 Hydrogen chloride-organic compound systems, 13 818... 

Triazolo[4,3-a][l,3,5]triazine-3,5,7-triamine hydrogen chloride hydrate... 

This chloride is prepared by dissolving tin in concentrated hydrochloric acid on cooling, the solution deposits crystals of hydrated tin(II) chloride. SnClj. 2H2O ("tin salt ). The anhydrous chloride is prepared by heating tin in a current of hydrogen chloride ... 

In both reactions above, the oxide dichloride is refluxed with the acid or the hydrated chloride the sulphur dioxide and hydrogen chloride pass off and any unused sulphur oxide dichloride is distilled off in vacuo. 

Uses ndReactions. Dihydromyrcene is used primarily for manufacture of dihydromyrcenol (25), but there are no known uses for the pseudocitroneUene. Dihydromyrcene can be catalyticaUy hydrated to dihydromyrcenol by a variety of methods (103). Reaction takes place at the more reactive tri-substituted double bond. Reaction of dihydromyrcene with formic acid gives a mixture of the alcohol and the formate ester and hydrolysis of the mixture with base yields dihydromyrcenol (104). The mixture of the alcohol and its formate ester is also a commercially avaUable product known as Dimyrcetol. Sulfuric acid is reported to have advantages over formic acid and hydrogen chloride in that it is less compUcated and gives a higher yield of dihydromyrcenol (105). 

Zirconium oxychloride is an important intermediate from which other zirconium chemicals are produced. It readily effloresces, and hydrates with 5—7 H2O are common. The salt caimot be dried to the anhydrous form, and decomposes to hydrogen chloride and zirconium oxide. 

BeryUium chloride [7787-47-5], BeCl2, is prepared by heating a mixture of beryUium oxide and carbon in chloride at 600—800°C. At pressures of 2.7—6.7 Pa (0.02—0.05 mm Hg) beryllium chloride sublimes at 350—380°C. It is easily hydrolyzed by water vapor or in aqueous solutions. BeryUium chloride hydrate [14871-75-1] has been obtained by concentrating a saturated aqueous solution of the chloride in a stream of hydrogen chloride. ChloroberyUate compounds have not been isolated from aqueous solutions, but they have been isolated from anhydrous fused salt mixtures. 

CeOCl. The anhydrous cerous chloride [7790-86-5] can be made from the hydrated salt by suppressing oxyhahde formation during thermal dehydration by the presence of hydrogen chloride or ammonium chloride. The anhydrous salt is soluble in a variety of organic solvents, eg, alcohols and ethers, has mp 817°C, and can be volatilized at high temperatures in vacuum. 

Chloroform and water at 0°C form six-sided crystals of a hydrate, CHCl I8H2O [67922-19-41which decompose at 1.6°C. Chloroform does not decompose appreciably when in prolonged contact with water at ordinary temperature and in the absence of air. However, on prolonged heating with water at 225°C, decomposition to formic acid, carbon monoxide, and hydrogen chloride occurs. A similar hydrolysis takes place when chloroform is decomposed at elevated temperature by potassium hydroxide. 

With Acyl Halides, Hydrogen Halides, and Metallic Halides. Ethylene oxide reacts with acetyl chloride at slightly elevated temperatures in the presence of hydrogen chloride to give the acetate of ethylene chlorohydrin (70). Hydrogen haUdes react to form the corresponding halohydrins (71). Aqueous solutions of ethylene oxide and a metallic haUde can result in the precipitation of the metal hydroxide (72,73). The haUdes of aluminum, chromium, iron, thorium, and zinc in dilute solution react with ethylene oxide to form sols or gels of the metal oxide hydrates and ethylene halohydrin (74). 

Toluenesulfonylhydrazide has been prepared by shaking 50% hydrazine hydrate and / -toluenesulfonyl chloride in benzene for several hours. Ammonia has been used as an agent for removing the hydrogen chloride evolved. ... 

Hindered rotation, 33, 34 internal, 367 Homopolymer, 168, 183 Hot bands, 374 Hot lattice, 4, 11, 21 Hydrates, 7, 9, 21, 31, 41 crystallization, 44 Hydrochloric acid clathrates, 2 in hydroquinone, 7 Hydrogen, bound, 4, 175 bromine hydrate, 35 4- carbon dioxide system, 110 4 carbon monoxide system, 96, 108 chloride hydrate, 35 clathrates, 2 chloride, 30... 

Butyrchloral has been prepared by chlorination of acetaldehyde 2 and of paraldehyde. Butyrchloral hydrate has been prepared by treatment of a,j8-dichlorobutyraldehyde with chlorine and water.3 Butyrchloral has also been prepared4 by treatment of crotonaldehyde with hydrogen chloride followed by chlorination. Brown and Plump have used a procedure similar to the one described here.3... 

Naphthalenedithiol can be prepared by adding 1,5-naph-thalenedisulfonyl chloride to an ethanol solution of tin (II) chloride 2-hydrate saturated with hydrogen chloride.6 An 80% yield of the crude dithiol melting at 103° was previously reported using zinc dust and sulfuric acid.7... 

Radon forms a series of clathrate compounds (inclusion compounds) similar to those of argon, krypton, and xenon. These can be prepared by mixing trace amounts of radon with macro amounts of host substances and allowing the mixtures to crystallize. No chemical bonds are formed the radon is merely trapped in the lattice of surrounding atoms it therefore escapes when the host crystal melts or dissolves. Compounds prepared in this manner include radon hydrate, Rn 6H20 (Nikitin, 1936) radon-phenol clathrate, Rn 3C H 0H (Nikitin and Kovalskaya, 1952) radon-p-chlorophenol clathrate, Rn 3p-ClC H 0H (Nikitin and Ioffe, 1952) and radon-p-cresol clathrate, Rn bp-CH C H OH (Trofimov and Kazankin, 1966). Radon has also been reported to co-crystallize with sulfur dioxide, carbon dioxide, hydrogen chloride, and hydrogen sulfide (Nikitin, 1939). 

Pechiney H+ A process for extracting aluminum from clays and other aluminous ores and wastes by hydrochloric acid. The ore is first attacked by sulfuric acid and a hydrated aluminum chloride sulfate is isolated. Sparging a solution of this with hydrogen chloride precipitates aluminum trichloride hexahydrate, which is pyrohydrolyzed in two stages. Invented in 1977 by J. Cohen and A. Adjemian at Aluminium Pechiney, France, and subsequently developed in association with Alcan. Piloted in France but not yet commercialized. 

Dichloroacetamide has been prepared from ethyl dichloroace-tate with alcoholic ammonia1 or aqueous ammonium hydroxide,2 from ethyl dichloromalonate and alcoholic ammonia,3 by the action of ammonia on pentachloroacetone,4 chloral cyanohydrin,5 and hexachloro-i,3,5-cyclohexanetrione,6 from chloral ammonia and potassium cyanide,7 by the action of hydrogen chloride on dichloroacetonitrile,8 from the reaction of asparagine with the sodium salt of N-chloro- -toluenesulfonamide,9 and by the action of an alkali cyanide and ammonia on chloral hydrate.10... 

This is prepared by passing dry hydrogen chloride over chromium, or hydrogen over anhydrous chromium(III) chloride. It is a white solid. If pure chromium is dissolved in dilute hydrochloric acid in the absence of air, a blue solution of the hydrated chloride, containing the hexaaquo-ion [Cr(H20)6]2+. is obtained. The same solution is also obtained by reduction of the + 6 oxidation state (through the + 3) using a solution of a dichromate(VI) and reducing with zinc and hydrochloric acid ... 

Formaldehyde reacted with hydrogen chloride in moist air to form 5ym-dichloromethyl ether. This compound may also form from an acidic solution containing chloride ions and formaldehyde (Frankel et al, 1974 Travenius, 1982). In an aqueous solution at 25 °C, nearly all the formaldehyde added is hydrated forming a gem-diol (Bell and McDougall, 1960). May polymerize in an aqueous solution to trio methylene (Hartley and Kidd, 1987). 

For a decade or so [CoH(CN)5] was another acclaimed catalyst for the selective hydrogenation of dienes to monoenes [2] and due to the exclusive solubility of this cobalt complex in water the studies were made either in biphasic systems or in homogeneous aqueous solutions using water soluble substrates, such as salts of sorbic add (2,4-hexadienoic acid). In the late nineteen-sixties olefin-metal and alkyl-metal complexes were observed in hydrogenation and hydration reactions of olefins and acetylenes with simple Rii(III)- and Ru(II)-chloride salts in aqueous hydrochloric acid [3,4]. No significance, however, was attributed to the water-solubility of these catalysts, and a new impetus had to come to trigger research specifically into water soluble organometallic catalysts. 

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