Tetrachloride sentence example

tetrachloride
  • When, as in the formation of naphthalene tetrachloride, for example, the one ring becomes saturated, the other might be expected to assume the normal centric form and become relatively inactive.

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  • The best solvents for rubber are carbon bisulphide, benzol and mineral naphtha, carbon tetrachloride and chloroform.

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  • If a suspension of lead dichloride in hydrochloric acid be treated with chlorine gas, a solution of lead tetrachloride is obtained; by adding ammonium chloride ammonium plumbichloride, (NH 4) 2 PbC1 6, is precipitated, which on treatment with strong sulphuric acid yields lead tetrachloride, PbC1 4, as a translucent, yellow, highly refractive liquid.

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  • A colloidal or soluble stannic acid is obtained by dialysing a mixture of tin tetrachloride and alkali, or of sodium stannate and hydrochloric acid.

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  • Stannic Chloride, SnC1 4, named by Andreas Libavius in 1605 Spiritus argenti vivi sublimate from its preparation by distilling tin or its amalgam with corrosive sublimate, and afterwards termed Spiritus fumans Libavii, is obtained by passing dry chlorine over granulated tin contained in a retort; the tetrachloride distils over as a heavy liquid, from which the excess of chlorine is easily removed by shaking with a small quantity of tin filings and re-distilling.

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  • Two chlorides are known, the dichloride, TeC121 and the tetrachloride, TeCl 4.

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  • They are both obtained by passing chlorine over tellurium, the product being separated by distillation (the tetrachloride is the less volatile).

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  • The tetrachloride is a white crystalline solid which is formed by the action of chlorine on the dichloride or by sulphur chloride on the element.

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  • Tellurous acid, H 2 TeO 3, is obtained when the tetrachloride is decomposed by water, or on dissolving tellurium in nitric acid and pouring the solution into water.

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  • There is a vast amount of literature on the subject, but in spite of the difficulty of conceiving a luminous carbon vapour at the temperature of an ordinary carbon flame, the evidence seems to show that no other element is necessary for its production as it is found in the spectrum of pure carbon tetrachloride and certainly in cases where chlorine is excluded.

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  • It readily forms addition products with chlorine and with hydrogen; the dichloride, C10H8C12, is obtained as a yellow liquid by acting with hydrochloric acid and potassium chlorate; the solid tetrachloride, C,o 11 8 C1 4, results when chlorine is passed into naphthalene dissolved in chloroform.

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  • Considerable interest is attached to the remarkable series of hydrocarbons obtained by Gomberg (Ber., 1900, 33, p. 3150, et seq.) by acting on triphenylmethane chloride (from triphenylmethane carbinol and phosphorus pentachloride, or from carbon tetrachloride and benzene in the presence of aluminium chloride) and its homologues with zinc, silver or mercury.

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  • Tungsten dioxide, W02, formed on reducing the trioxide by hydrogen at a red heat or a mixture of the trioxide and hydrochloric acid with zinc, or by decomposing the tetrachloride with water, is a brown strongly pyrophoric powder, which must be cooled in hydrogen before being brought into contact with air.

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  • The dichloride, WC1 2, is an amorphous grey powder obtained by reducing the hexachloride at a high temperature in hydrogen, or, better, by heating the tetrachloride in a current of carbon dioxide.

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  • The tetrachloride, WC1 41 is obtained by partial reduction of the higher chlorides with hydrogen; a mixture of the pentaand hexa-chloride is distilled in a stream of hydrogen or carbon dioxide, and the pentachloride which volatilizes returned to the flask several times.

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  • This gives the tetrachloride as a greyishbrown crystalline powder.

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  • It is more hygroscopic than the tetrachloride; and when treated with much water the bulk is at once decomposed into the blue oxide and hydrochloric acid, but an olive-green solution is also produced.

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  • Bismuth and antimony chlorides are decomposed by water with production of oxychlorides, whilst titanium tetrachloride yields titanic acid under the same conditions.

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  • Silicobenzoic acid, C 6 H 5 S10.0H, results from the action of dilute aqueous ammonia on phenyl silicon chloride (obtained from mercury diphenyl and silicon tetrachloride).

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  • The pentachloride, WC1 5, is obtained as a product in the preparation of the tetrachloride.

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  • Vanadium dichloride, VC12, is a green crystalline solid obtained when the tetrachloride is reduced with hydrogen at a dull red heat.

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  • The tetrachloride, VC14, is formed by the direct union of vanadium and chlorine or by the action of sulphur chloride on vanadium pentoxide (Matignon, Comptes rendus, 1904, 138, p. 631).

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  • They are completely soluble in ether, carbon bisulphide, chloroform, carbon tetrachloride, petroleum ether, and benzene.

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  • Carbon tetrachloride, chloroform, acetone and benzene are far too expensive.

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  • Carbon tetrachloride would be an ideal solvent, as it is non-inflammable and shares with carbon bisulphide the advantage of being heavier than water.

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  • This indicates the percentage of iodine absorbed by an oil or fat when the latter is dissolved in chloroform or carbon tetrachloride, and treated with an accurately measured amount of free iodine supplied in the form of iodine chloride.

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  • Silicon tetrachloride is a colorless liquid at room temperature which fumes in moist air.

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  • Suppose a water molecule is going to react with the carbon tetrachloride.

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  • If you add water to silicon tetrachloride, there is a violent reaction to produce silicon dioxide and fumes of hydrogen chloride.

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  • The injuries were caused by the leak of titanium tetrachloride from a tanker.

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  • The corresponding hydroxide, Ir(OH) 4, is formed when potassium iridate is boiled with ammonium chloride, or when the tetrachloride is boiled with caustic potash or sodium carbonate.

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  • Lengyel, Ber., 1869, 2, P. 54), 4CHC13+302= 40001 2 +2H 2 O+2C1 2 i or most conveniently by heating carbon tetrachloride with fuming sulphuric acid (H.

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  • Phthalic acid was obtained by Laurent in 1836 by oxidizing naphthalene tetrachloride, and, believing it to be a naphthalene derivative, he named it naphthalenic acid; Marignac determined its formula and showed Laurent's supposition to be incorrect, upon which Laurent gave it its present name.

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  • Iridium tetrachloride, IrC1 41 is obtained by dissolving the finely divided metal in aqua regia; by dissolving the hydroxide in hydrochloric acid; and by digesting the hydrated sesquichloride with nitric acid.

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