Chloride dihydrate

Alternatively, the equivalent quantity of palladium chloride dihydrate may be used. 

A cousin to this reduction is one using stannous chloride (a.k.a. SnCb, a.k.a. Tin chloride) which is done exactly as the calcium one except that about lOOg of SnCb is used in place of the Mg or Ca and the addition occurs at room temperature and the solution is stirred for one hour rather than 15 minutes. Some very good reductions that operate almost exclusively at room temperature with no pressure and give almost 100% yields are to follow. The only reason Strike did not detail these methods is that some of the chemicals involved are a little less common than Strike is used to but all are available to the public. These alternatives include acetlylacetone and triethylamine [73], propanedithlol and trieth-ylamine [74], triphenylphosphine [75], NaBH4 with phase transfer catalyst [76], H2S and pyridine [77], and palladium hydrox-ide/carbon with hydrazine [78], stannous chloride dihydrate [85]. 

Saturation temperatures of sodium chloride dihydrate at these temperatures NaCl 2H2O separates leaving the brine of the eutectic composition (E). 

Stannous Chloride. Stannous chloride is available in two forms anhydrous stannous chloride, SnCl2, and stannous chloride dihydrate [10025-69-1], SnCl2 2H20, also called tin crystals or tin salts. These forms are sometimes used interchangeably however, where stabiUty, concentration, and adaptabihty are important, anhydrous stannous chloride is preferred. Even after long storage, changes in the stannous tin content of anhydrous stannous chloride are extremely low. Physical properties of the tin chlorides are Hsted in Table 1. 

Stannous Chloride Dihydrate. A white crystalline soHd, stannous chloride dihydrate is prepared either by treatment of granulated tin with hydrochloric acid followed by evaporation and crystallisation or by reduction of a stannic chloride solution with a cathode or tin metal followed by crystallisation. It is soluble in methanol, ethyl acetate, glacial acetic acid, sodium hydroxide solution, and dilute or concentrated hydrochloric acid. It is soluble in less than its own weight of water, but with much water it forms an insoluble basic salt. 

The CASS Test. In the copper-accelerated acetic acid salt spray (CASS) test (42), the positioning of the test surface is restricted to 15 2°, and the salt fog corrosivity is increased by increasing temperature and acidity, pH about 3.2, along with the addition of cupric chloride dihydrate. The CASS test is used extensively by the U.S. automobile industry for decorative nickel—chromium deposits, but is not common for other deposits or industries. Exposure cycle requirements are usually 22 hours, rarely more than 44 hours. Another corrosion test, now decreasing in use, for decorative nickel—chromium finishes is the Corrodkote test (43). This test utilizes a specific corrosive paste combined with a warm humidity cabinet test. Test cycles are usually 20 hours. 

Lower temperatures may induce the solid methylene chloride dihydrate to separate and interfere with stirring. An acetone bath into which lumps of Dry Ice are introduced as required affords easily controlled cooling. 

Chemical Designations - Synonyms Cobalt (II) Chloride Cobaltous Chloride Cobaltous Chloride Dihydrate Cobaltous Chloride Hexahydrate Chemical Formula CoClj,... 

After the addition had been completed, the acidic solution containing p-acetylphenyldiazo-nium chloride formed in the above reaction was added dropwise with stirring to a mixture of 530 ml of glacial acetic acid and 530 ml of benzene which had been previously cooled, and the cooled solution saturated with sulfur dioxide and to which had been added 34 g of cupric chloride dihydrate. After the addition had been completed, the reaction mixture was stirred at about 40°C for three hours, and was then poured into 3,000 ml of an ice-water mixture. 

A hot, filtered solution of 2.27 grams of pyrvinium chloride dihydrate in 250 ml of water is added slowly to a solution of 2.25 grams of sodium pamoate monohydrate in 50 ml of water. A red precipitate immediately forms. The mixture is heated at about 90°-100°C for 5 minutes more and then filtered. The reaction product is washed with hot water and dried at about 75°C in a vacuum. This preparation melts at about 210°-215°C with prior softening from about 190°C. 

Tin(II) chloride solution. Dissolve lOg of tin(II) chloride dihydrate in 100mL of 1M hydrochloric acid. 

A solution of 257 g. (1.05 moles) of barium chloride dihydrate in about 500 cc. of hot water is added to the reaction mixture, with vigorous shaking, and the mixture is heated on a steam bath for one-half hour. A heavy precipitate of the barium salt of the amino acid separates at once. After cooling to room temperature, the barium salt is collected on a suction filter, transferred to a beaker, and washed with two 250-cc. portions of hot water (8o°). After drying at ioo°, the barium salt weighs 225-230 g. (80-82 per cent of the theoretical amount). 

Chromium, tetraaquadichloro-chloride dihydrate hydrate isomerism, 1, 183 Chromium, tetrabromo-solvated, 3, 758 synthesis, 3, 763 Chromium, tetrachloro-antiferromagnetic, 3, 761 ferromagnetic magnetic properties, 3,7559 optical properties, 3,759 structure, 3,759 solvated, 3. 758 synthesis. 3, 759 Chromium, tetrachlorooxy-tetraphenylarsenate stereochemistry, 1,44 Chromium, tetrahalo-, 3,889 Chromium, tetrakis(dioxygen)-stereochemistry, 1,94 Chromium, triamminediperoxy-structure. 1, 78 Chromium, tricyanodiperoxy-structure, 1, 78 Chromium, trifluoro-electronic spectra, 3, 757 magnetic properties, 3, 757 structures, 3, 757 synthesis, 3, 756 Chromium, trihalo-clcctronic spectra, 3, 764 magnetic properties, 3, 764 structure, 3, 764 synthesis, 3, 764 Chromium, tris(acetylacetone)-structure. 1, 65 Chromium, tris(bipyridyl)-... 

Tin, nitratodiphenyltris(dimethy) sulfoxide)-structure, 1,77 Tin, nitratotris(triphenyltin)-structure, 1, 47 Tin,tetrakis(acetato)-stereochemistry, 1,94 Tin, tetrakis(diethyldithiocarbamato)-angular parameters, 1, 57 Tin, tetrakis(ethyldithiocarbamato)-angular parameters, 1, 57 Tin, tetranitrato-stereochemistry, 1, 94 Tin, tri-n-butylmethoxy-, 3, 208 Tin alkoxides physical properties, 2, 346 Tin bromide, 3, 194 Tin bromide hydrate, 3,195 Tin carboxylates, 3, 222 mixed valence, 3, 222 Tin chloride, 3, 194 hydroformylation platinum complexes, 6, 263 Tin chloride dihydrate, 3,195 Tin complexes, 3, 183-223 acetyl ace tone... 

Polycondensation At room temperature, 0.4% mass of Sn(II) chloride dihydrate (SnCl2-2H20) and 0.4% mass of p-toluenesulfonic acid monohydrate (p-TSA) are introduced into the mixture. The mixture is heated to 180°C under mechanical stirring. The pressure is reduced stepwise to reach 13 mbar, and file reaction is continued for 20 h. The reaction system becomes gradually viscous, and a small amount of L-lactide is formed and refluxed through the reflux condenser. At file end of the reaction, the flask is cooled down, file product is dissolved in chloroform and subsequently precipitated into diethyl ether. The resulting white fibrous solids are filtered and dried under vacuum (average yield 67%). 

Answer (a) Nickel(II) chloride dihydrate (b) aluminum fluoride ... 

E.28 A chemist wants to extract the gold from 35.25 g of gold(III) chloride dihydrate, AuCI3-2H20, by electrolysis of an aqueous solution (this technique is described in Chapter 12). What mass of gold could be obtained from the sample ... 

Dipping solution 1 Dissolve 2 g tin(II) chloride dihydrate in 20 ml hydrochloric acid (2S[Pg.62]

C03-0015. Determine the chemical formulas of barium chloride dihydrate, chromium(III) hydroxide, and sulfur trioxide. 

Hydrochloric acid, 37%, Merck, code 317, or equivalent Stannous chloride dihydrate, Merck, code 7815, or equivalent Cupric acetate monohydrate, Merck, code 2711, or equivalent Lead acetate trihydrate, Merck, code 7372, or equivalent... 

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