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  2. Hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_cyanide

    CH 4 + NH 3 → HCN + 3H 2. This reaction is akin to steam reforming, the reaction of methane and water to give carbon monoxide and hydrogen. In the Shawinigan Process, hydrocarbons, e.g. propane, are reacted with ammonia. In the laboratory, small amounts of HCN are produced by the addition of acids to cyanide salts of alkali metals: H + + CN ...

  3. Inorganic nonaqueous solvent - Wikipedia

    en.wikipedia.org/wiki/Inorganic_nonaqueous_solvent

    An acid which has more of a tendency to donate a hydrogen ion than the limiting acid will be a strong acid in the solvent considered, and will exist mostly or entirely in its dissociated form. Likewise, the limiting base in a given solvent is the solvate ion, such as OH − ion, in water. A base which has more affinity for protons than the ...

  4. Cyanide - Wikipedia

    en.wikipedia.org/wiki/Cyanide

    Cyanide is unstable in water, but the reaction is slow until about 170 °C. It undergoes hydrolysis to give ammonia and formate, which are far less toxic than cyanide: [14] CN − + 2 H 2 O → HCO − 2 + NH 3. Cyanide hydrolase is an enzyme that catalyzes this reaction.

  5. Neutralization (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Neutralization_(chemistry)

    The same equation relating the concentrations of acid and base applies. The concept of neutralization is not limited to reactions in solution. For example, the reaction of limestone with acid such as sulfuric acid is also a neutralization reaction. [Ca,Mg]CO 3 (s) + H 2 SO 4 (aq) → (Ca 2+, Mg 2+)(aq) + SO 2− 4 (aq) + CO 2 (g) + H 2 O

  6. Aqueous solution - Wikipedia

    en.wikipedia.org/wiki/Aqueous_solution

    This reaction occurs when two aqueous strong electrolyte solutions mix and produce an insoluble solid, also known as a precipitate. The ability of a substance to dissolve in water is determined by whether the substance can match or exceed the strong attractive forces that water molecules generate between themselves.

  7. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    In transhydrocyanation, an equivalent of HCN is transferred from a cyanohydrin, e.g. acetone cyanohydrin, to another activated HCN acceptor. The transfer is an equilibrium process, initiated by base. The reaction can be driven by trapping or a superior acceptor, such as an aldehyde. [9]

  8. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    In chemistry, a hydration reaction is a chemical reaction in which a substance combines with water. In organic chemistry, water is added to an unsaturated substrate, which is usually an alkene or an alkyne. This type of reaction is employed industrially to produce ethanol, isopropanol, and butan-2-ol. [1]

  9. Glycolonitrile - Wikipedia

    en.wikipedia.org/wiki/Glycolonitrile

    It is a colourless liquid that dissolves in water and ether. Because glycolonitrile decomposes readily into formaldehyde and hydrogen cyanide , it is listed as an extremely hazardous substance . In January 2019, astronomers reported the detection of glycolonitrile, another possible building block of life among other such molecules , in outer ...

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