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  2. 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.

  3. Air-free technique - Wikipedia

    en.wikipedia.org/wiki/Air-free_technique

    Where air-free requirements are not stringent, other techniques can be used. For example, using a sacrificial excess of a reagent that reacts with water/oxygen can be used. The sacrificial excess in effect "dries" the reaction by reacting with the water (e.g. in the solvent).

  4. Pyrophoricity - Wikipedia

    en.wikipedia.org/wiki/Pyrophoricity

    Metal hydrides (sodium hydride, lithium aluminium hydride, uranium trihydride) Partially or fully alkylated derivatives of metal and nonmetal hydrides (diethylaluminium hydride, trimethylaluminium, triethylaluminium, butyllithium), with a few exceptions (i.e. dimethylmercury and tetraethyllead) Copper fuel cell catalysts (zinc oxide, aluminium ...

  5. Water-reactive substances - Wikipedia

    en.wikipedia.org/wiki/Water-reactive_substances

    Group 1: Alkali metals Reaction of sodium (Na) and water Reaction of potassium (K) in water. The alkali metals (Li, Na, K, Rb, Cs, and Fr) are the most reactive metals in the periodic table - they all react vigorously or even explosively with cold water, resulting in the displacement of hydrogen.

  6. Hydride - Wikipedia

    en.wikipedia.org/wiki/Hydride

    The hydride adds to an electrophilic center, typically unsaturated carbon. Hydrides such as sodium hydride and potassium hydride are used as strong bases in organic synthesis. 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 ...

  7. Sodium borohydride - Wikipedia

    en.wikipedia.org/wiki/Sodium_borohydride

    Sodium borohydride is an odorless white to gray-white microcrystalline powder that often forms lumps. It can be purified by recrystallization from warm (50 °C) diglyme. [10] Sodium borohydride is soluble in protic solvents such as water and lower alcohols. It also reacts with these protic solvents to produce H 2; however, these reactions are ...

  8. Sodium amide - Wikipedia

    en.wikipedia.org/wiki/Sodium_amide

    Sodium amide is a common reagent with a long history of laboratory use. [9] It can decompose violently on contact with water, producing ammonia and sodium hydroxide: NaNH 2 + H 2 O → NH 3 + NaOH. When burned in oxygen, it will give oxides of sodium (which react with the produced water, giving sodium hydroxide) along with nitrogen oxides:

  9. Potassium hydride - Wikipedia

    en.wikipedia.org/wiki/Potassium_hydride

    KH reacts with water according to the reaction: KH + H 2 O → KOH + H 2. As a superbase, potassium hydride is more basic than sodium hydride. It is used to deprotonate certain carbonyl compounds to give enolates. It also deprotonates amines to give the corresponding amides of the type KNHR and KNR 2. [6]