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Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).
When derived from hydrazine itself, hydrazones condense with a second equivalent of a carbonyl to give azines: [11] R 2 C=N−NH 2 + R 2 C=O → R 2 C=N−N=CR 2 + H 2 O. Hydrazones are intermediates in the Wolff–Kishner reduction. Hydrazones are reactants in hydrazone iodination, the Shapiro reaction, and the Bamford–Stevens reaction to ...
The modified procedure consists of refluxing the carbonyl compound in 85% hydrazine hydrate with three equivalents of sodium hydroxide followed by distillation of water and excess hydrazine and elevation of the temperature to 200 °C. Significantly reduced reaction times and improved yields can be obtained using this modification.
Over twenty other hydrides of nitrogen are known, the most important being hydrazine (N 2 H 4) and hydrogen azide (HN 3). Hydrazine has physical properties that are remarkably similar to those of water: its melting and boiling points are 2.0 °C and 113.5 °C, the density of the solid at −5 °C is 1.146 g/cm 3 , while that of the liquid at 25 ...
Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou
diazane (or hydrazine), N 2 H 4 - two nitrogen and four hydrogen triazane, N 3 H 5 - three nitrogen and five hydrogen. Azanes with three or more nitrogen atoms are named by adding the suffix-azane to the appropriate numerical multiplier prefix. Hence, triazane, N 3 H 5; tetrazane or tetraazane, N 4 H 6; pentazane or pentaazane, N 5 H 7 ...
Phenylhydrazine was the first hydrazine derivative characterized, reported by Hermann Emil Fischer in 1875. [7] [8] He prepared it by reduction of a phenyl diazonium salt using sulfite salts. Fischer used phenylhydrazine to characterize sugars via formation of hydrazones known as osazones with the sugar aldehyde. He also demonstrated in this ...
It is an intermediate in some hydrazine manufacturing processes. Synthesis. Acetone azine can be prepared from acetone and hydrazine: [3] 2 (CH 3) 2 CO + N 2 H 4 → ...