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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".
Reductions with hydrosilanes are methods used for hydrogenation and hydrogenolysis of organic compounds.The approach is a subset of ionic hydrogenation.In this particular method, the substrate is treated with a hydrosilane and auxiliary reagent, often a strong acid, resulting in formal transfer of hydride from silicon to carbon. [1]
A metal hydride can be a thermodynamically a weak acid and a weak H − donor; it could also be strong in one category but not the other or strong in both. The H − strength of a hydride also known as its hydride donor ability or hydricity corresponds to the hydride's Lewis base strength. Not all hydrides are powerful Lewis bases.
Calcium hydride is the chemical compound with the formula CaH 2, an alkaline earth hydride. This grey powder (white if pure, which is rare) reacts vigorously with water, liberating hydrogen gas. CaH 2 is thus used as a drying agent, i.e. a desiccant. [2] CaH 2 is a saline hydride, meaning that its structure is salt-like. The alkali metals and ...
Lithium aluminium hydride also reduces alkyl halides to alkanes. [36] [37] Alkyl iodides react the fastest, followed by alkyl bromides and then alkyl chlorides. Primary halides are the most reactive followed by secondary halides. Tertiary halides react only in certain cases. [38] Lithium aluminium hydride does not reduce simple alkenes or arenes.
In this reaction ACCN is a radical initiator and an aliphatic thiol transfers radical character to the silylhydride. The triethylsilyl free radical then reacts with the azide with expulsion of nitrogen to a N-silylarylaminyl radical which grabs a proton from a thiol completing the catalytic cycle:
Stryker's reagent ([(PPh 3)CuH] 6), [1] also known as the Osborn complex, is a hexameric copper hydride ligated with triphenylphosphine. It is a brick red, air-sensitive solid. Stryker's reagent is a mildly hydridic reagent, used in homogeneous catalysis of conjugate reduction reactions of enones, enoates, and related substrates.
The β-diketiminato germylene hydride is reported to react with several alkynes, including ethyl propiolate to form a vinyl germylene in good yield (>80%). [7] [10] This reaction occurs via the 1,2-addition of the germylene hydride across the alkyne triple bond, as opposed to an H 2 elimination involving one of the C-H bonds of the alkyne. This ...