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  2. Hydride - Wikipedia

    en.wikipedia.org/wiki/Hydride

    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".

  3. Transition metal hydride - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_hydride

    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 ...

  4. Aluminium hydride - Wikipedia

    en.wikipedia.org/wiki/Aluminium_hydride

    Aluminium hydride reduces acetals to half protected diols. [1] Acetal reduction using aluminium hydride. Aluminium hydride reduces epoxide to the corresponding alcohol: [1] Epoxide reduction using aluminium hydride. The allylic rearrangement reaction carried out using aluminium hydride is a S N 2 reaction, and it is not sterically demanding: [1]

  5. Hydrogen anion - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_anion

    The term hydride is probably most often used to describe compounds of hydrogen with other elements in which the hydrogen is in the formal −1 oxidation state. In most such compounds the bonding between the hydrogen and its nearest neighbor is covalent. An example of a hydride is the borohydride anion (BH − 4).

  6. Potassium hydride - Wikipedia

    en.wikipedia.org/wiki/Potassium_hydride

    Potassium hydride, KH, is the inorganic compound of potassium and hydrogen. It is an alkali metal hydride. It is a white solid, although commercial samples appear gray. It is a powerful superbase that is useful in organic synthesis. It is sold commercially as a slurry (~35%) in mineral oil or sometimes paraffin wax to facilitate dispensing. [3]

  7. Binary compounds of hydrogen - Wikipedia

    en.wikipedia.org/wiki/Binary_compounds_of_hydrogen

    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.

  8. Lithium hydride - Wikipedia

    en.wikipedia.org/wiki/Lithium_hydride

    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 ...

  9. Sodium hydride - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydride

    Sodium hydride is the chemical compound with the empirical formula Na H. This alkali metal hydride is primarily used as a strong yet combustible base in organic synthesis . NaH is a saline (salt-like) hydride , composed of Na + and H − ions, in contrast to molecular hydrides such as borane , silane , germane , ammonia , and methane .