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azoimide

azoimide Sentence Examples

  • 4468 of 1908), and by lead azoimide (Hyronimus, Brit.

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  • Amongst endothermic compounds may be noted hydriodic acid, HI, acetylene, C 2 H 2, nitrous oxide, N 2 O, nitric oxide, NO, azoimide, N 3 H, nitrogen trichloride, NC1 3.

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  • Nitrogen combines with hydrogen to form ammonia, NH 3, hydrazine, N 2 H 4, and azoimide, N 3 H (qq.v.); the other known hydrides, N 4 H 4 and N5H5, are salts of azoimide, viz.

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  • Its ethyl ester reacts with hydrazine to form hippuryl hydrazine, C,H 5 CO NH CH 2 CO NH NH 2, which was used by Curtius for the preparation of azoimide.

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  • Heated in a current of carbon dioxide sodamide yields caustic soda and cyanamide, and with nitrous oxide it gives sodium azoimide; it deflagrates with lead or silver nitrate and explodes with potassium chlorate.

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  • Azoimide >>

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  • Diazoimino compounds, R N3, may be regarded as derivatives of azoimide; they are formed by the action of ammonia on the diazoperbromides,or by the action of hydroxylamine on the diazonium sulphates (J.

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  • The nitride AgN3, silver azoimide, is also highly explosive.

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  • AZOIMIDE, or Hydra701c Acid, N3h, a compound of nitrogen and hydrogen, first isolated in 1890 by Th.

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  • Grandmougin (Berichte, 1891, 24, p. 2546) obtained azoimide from dinitraniline, C 6 H 3 (NO 2) 2 NH 2j by diazotization and conversion of the diazo compound into the perbromide, (NO 2) 2 C 6 H 3 N 2 Br 3.

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  • The solution is then acidified and distilled, when azoimide passes over.

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  • After the greater portion of the alcohol has distilled off, the solution is acidified with sulphuric acid and the azoimide distilled over.

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  • Ammonium azoimide, N 3 NH 4j may be prepared by boiling diazohippuramide with alcoholic ammonia, until no more ammonia escapes, the following reaction taking place: C,H 5 CO [[Nhch 2 Conh N 2.

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  • Hydrazine azoimide, N 5 H 5, is also known.

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  • Chloroazoimide, C1 N 3, the chloride corresponding to azoimide, was obtained by F.

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  • It has been proposed to replace fulminate by silver azoimide (Wdhler & Matter, Brit.

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  • 4468 of 1908), and by lead azoimide (Hyronimus, Brit.

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  • Amongst endothermic compounds may be noted hydriodic acid, HI, acetylene, C 2 H 2, nitrous oxide, N 2 O, nitric oxide, NO, azoimide, N 3 H, nitrogen trichloride, NC1 3.

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  • Raschig in 1908 (see Azoimide); the corresponding iodine compound had been obtained in 1900 by A.

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  • Nitrogen combines with hydrogen to form ammonia, NH 3, hydrazine, N 2 H 4, and azoimide, N 3 H (qq.v.); the other known hydrides, N 4 H 4 and N5H5, are salts of azoimide, viz.

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  • Its ethyl ester reacts with hydrazine to form hippuryl hydrazine, C,H 5 CO NH CH 2 CO NH NH 2, which was used by Curtius for the preparation of azoimide.

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  • Heated in a current of carbon dioxide sodamide yields caustic soda and cyanamide, and with nitrous oxide it gives sodium azoimide; it deflagrates with lead or silver nitrate and explodes with potassium chlorate.

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  • Diazoimino compounds, R N3, may be regarded as derivatives of azoimide; they are formed by the action of ammonia on the diazoperbromides,or by the action of hydroxylamine on the diazonium sulphates (J.

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  • The nitride AgN3, silver azoimide, is also highly explosive.

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  • AZOIMIDE, or Hydra701c Acid, N3h, a compound of nitrogen and hydrogen, first isolated in 1890 by Th.

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  • Grandmougin (Berichte, 1891, 24, p. 2546) obtained azoimide from dinitraniline, C 6 H 3 (NO 2) 2 NH 2j by diazotization and conversion of the diazo compound into the perbromide, (NO 2) 2 C 6 H 3 N 2 Br 3.

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  • The solution is then acidified and distilled, when azoimide passes over.

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  • After the greater portion of the alcohol has distilled off, the solution is acidified with sulphuric acid and the azoimide distilled over.

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  • Ammonium azoimide, N 3 NH 4j may be prepared by boiling diazohippuramide with alcoholic ammonia, until no more ammonia escapes, the following reaction taking place: C,H 5 CO [[Nhch 2 Conh N 2.

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  • Hydrazine azoimide, N 5 H 5, is also known.

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  • Chloroazoimide, C1 N 3, the chloride corresponding to azoimide, was obtained by F.

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