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The hydride reacts with the weak Bronsted acid releasing H 2. Hydrides such as calcium hydride are used as desiccants, i.e. drying agents, to remove trace water from organic solvents. The hydride reacts with water forming hydrogen and hydroxide salt. The dry solvent can then be distilled or vacuum transferred from the "solvent pot".
Hydride vapour-phase epitaxy (HVPE) is an epitaxial growth technique often employed to produce semiconductors such as GaN, GaAs, InP and their related compounds, in which hydrogen chloride is reacted at elevated temperature with the group-III metals to produce gaseous metal chlorides, which then react with ammonia to produce the group-III nitrides.
The soluble hydride is susceptible to pyrolysis under vacuum and proceeds to completion under 100 °C. Amorphous copper hydride is also produced by anhydrous reduction. In this process copper(I) and tetrahydroaluminate react to produce molecular copper hydride and triiodoaluminium adducts.
Binary hydrogen compounds in group 1 are the ionic hydrides (also called saline hydrides) wherein hydrogen is bound electrostatically. Because hydrogen is located somewhat centrally in an electronegative sense, it is necessary for the counterion to be exceptionally electropositive for the hydride to possibly be accurately described as truly behaving ionic.
LiH reacts with sulfur dioxide to give the dithionite: 2 LiH + 2 SO 2 → Li 2 S 2 O 4 + H 2. though above 50 °C the product is lithium sulfide instead. [3]: 9 LiH reacts with acetylene to form lithium carbide and hydrogen. With anhydrous organic acids, phenols and acid anhydrides, LiH reacts slowly, producing hydrogen gas and the lithium salt ...
The reaction involves no changes in the oxidation state of the metal and can be viewed as splitting H 2 into hydride (which binds to the metal) and proton (which binds to the base). ML n x+ + base + H 2 ⇌ HML n (x-1)+ + Hbase + Such reaction are assumed to involve the intermediacy of dihydrogen complexes. Bifunctional catalysts activate H 2 ...
In its standard state arsine is a colorless, denser-than-air gas that is slightly soluble in water (2% at 20 °C) [1] and in many organic solvents as well. [citation needed] Arsine itself is odorless, [5] but it oxidizes in air and this creates a slight garlic or fish-like scent when the compound is present above 0.5 ppm. [6]
Mercury(II) hydride may be prepared by the reduction of mercury(II) chloride. In this process, mercury(II) chloride and a hydride salt equivalent react to produce mercury(II) hydride according to the following equations, which depend on the stoichiometry of the reaction: 2 HgCl 2 + 2 H − → HgCl 2− 4 + HgH 2 HgCl 2 + 2 H − → HgH 2 + 2 ...