Nitrous-acid sentence example

nitrous-acid
  • More important are Kekule's observations that nitrous acid oxidizes pyrocatechol or [I.2]-dioxybenzene, and protocatechuic acid or [3.4]- dioxybenzoic acid to dioxytartaric acid, (C(OH) 2 COOH) 2 (Ann., 1883, 221, p. 230); and 0.

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  • Meyer, which are formed when nitrous acid acts on primary aliphatic nitro compounds.

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  • In acid solution, potassium permanganate oxidizes it to nitric acid, but in alkaline solution only to nitrous acid.

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  • It may be prepared by the fusion of para-toluene sulphonic acid with potash; by the action of nitrous acid on para-toluidine; or by heating para-oxyphenyl acetic acid with lime.

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  • Both classes readily exchange the imide hydrogen for acid radicals, and give nitrosamines with nitrous acid.

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  • The three classes of diamines may be distinguished by their behaviour towards nitrous acid.

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  • It is obtained by the dry distillation of nitrogenous vegetable and animal products; by the reduction of nitrous acid and nitrites with nascent hydrogen; and also by the decomposition of ammonium salts by alkaline hydroxides or by slaked lime, the salt most generally used being the chloride (sal-ammoniac, q.v.) thus 2NH 4 C1+Ca(OH) 2 =CaC1 2 +2H 2 O+2NH 3.

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  • This corresponds to N+1 7 5 0, the oxygen being decidedly in excess of the proportion required to form nitrous acid.

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  • Diazosuccinic ester, N2 C(C02C2H5)2, is similarly prepared by the action of nitrous acid on the hydrochloride of aspartic ester.

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  • Alkaline hypobromites or hypochlorites or nitrous acid decompose urea into carbon dioxide and nitrogen.

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  • It may be synthetically prepared by the fusion of cymol sulphonic acid with caustic potash; by the action of nitrous acid on 1-methyl-2-amino-4-propyl benzene; by prolonged heating of 5 parts of camphor with r part of iodine; or by heating carvol with glacial phosphoric acid.

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  • Amidotetrazotic acid yields addition compounds with amines, and by the further action of nitrous acid yields a very explosive derivative, diazotetrazol, CN 3.

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  • His last chemical paper, published in 1788, on the "Conversion of a mixture of dephlogisticated and phlogisticated air into nitrous acid by the electric spark," describes measures he took to authenticate the truth of the experiment described in the 1785 paper, which had "since been tried by persons of distinguished ability in such pursuits without success."

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  • The orthoand parasemidines can be readily distinguished by their behaviour with different reagents; thus with nitrous acid the ortho-semidines give azimido compounds, whilst the para-semidines give complex diazo derivatives; with formic or acetic acids the ortho-semidines give anhydro compounds of a basic character, the para-semidines give acyl products possessing no basic character.

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  • It crystallizes in long needles; forms salts C5H5N5.2HI and (C5H5N5)2.H2SO4.2H2O, and is converted by nitrous acid into hypoxanthine or 6-oxypurin.

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  • Where the nitrous fumes prevail and there is less water present, sulphur dioxide combines with nitrous acid and oxygen to form nitroso-sulphuric acid, a crystalline substance of the formula SO 2 (OH)(ONO).

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  • The re-formed nitrous acid, although not stable, any more than is its anhydride, N203, is nevertheless the j` oxygen carrier" in question, as the products of its spontaneous decomposition, when meeting with other compounds, always react like nitrous acid itself and thus may transfer an indefinite quantity of oxygen to the corresponding quantities of SO 2 and H 2 O, with the corresponding formation of H2S04.

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  • Another method is based upon the different behaviour of the corresponding nitro-alkyl with nitrous acid.

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  • By this treatment a primary nitro-alkyl yields a nitrolic acid, the potassium salt of which forms an intense red solution; a secondary nitro-alkyl forms a pseudo nitrol, which gives an intense blue solution, while the tertiary compound does not act with nitrous acid.

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  • Primary alcohols are obtained by decomposing their sulphuric acid esters (from sulphuric acid and the olefines) with boiling water; by the action of nitrous acid on primary amines; or by the reduction of aldehydes, acid chlorides or acid anhydrides.

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  • An improved method of preparation was found in the use of hippuric acid, which reacts with hydrazine hydrate to form hippuryl hydrazine, C 6 H 5 [[Conh Ch 2 Conh Nh]] 2, and this substance is converted by nitrous acid into diazo-hippuramide, C 6 H 5 [[Conh Ch 2 Co Nh N 2.0h]], which is hydrolysed by the action of caustic alkalis with the production of salts of hydrazoic acid.

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  • When warmed with a solution of nitrous acid, they are converted into phenols; if, however, nitrous acid be added to an ice-cold solution of a primary amine in excess of mineral acid, a diazonium salt is formed (see Az o Compounds and DIAzO Compounds), or in absence of excess of acid, a diazoamine is produced.

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  • Chiozza, Ann., 1852, 83, p. 118) or with ferrous sulphate and baryta, and kynurine (-y-oxyquinoline), which is obtained by the action of nitrous acid on y-aminoquinoline (A.

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