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  2. Hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_cyanide

    Hydrogen cyanide (formerly known as prussic acid) is a chemical compound with the formula HCN and structural formula H−C≡N.It is a highly toxic and flammable liquid that boils slightly above room temperature, at 25.6 °C (78.1 °F).

  3. Cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin

    RR’C=O + HCN → RR’C(OH)CN. In this reaction, the nucleophilic CN − ion attacks the electrophilic carbonyl carbon in the ketone, followed by protonation by HCN, thereby regenerating the cyanide anion. Cyanohydrins are also prepared by displacement of sulfite by cyanide salts: [2] Cyanohydrins are intermediates in the Strecker amino acid ...

  4. Cyanohydrin reaction - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin_reaction

    This nucleophilic addition is a reversible reaction but with aliphatic carbonyl compounds equilibrium is in favor of the reaction products. The cyanide source can be potassium cyanide (KCN), sodium cyanide (NaCN) or trimethylsilyl cyanide ((CH 3) 3 SiCN). With aromatic aldehydes such as benzaldehyde, the benzoin condensation is a

  5. Andrussow process - Wikipedia

    en.wikipedia.org/wiki/Andrussow_process

    The change of enthalpy of this reaction is equal to -481.06 kJ. [3] The heat provided by the main reaction serves as a catalyst for other side reactions. CH 4 + H 2 O → CO + 3 H 2 2 CH 4 + 3 O 2 → 2 CO + 4 H 2 O 4 NH 3 + 3 O 2 → 2 N 2 + 6 H 2 O. These side reactions can be minimized by only short exposures to the catalyst of the order of ...

  6. 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 − ( hydroxide ) ion, in water.

  7. Cyanide - Wikipedia

    en.wikipedia.org/wiki/Cyanide

    This reaction is the basis of cyanide's toxicity. [19] The high affinities of metals for this anion can be attributed to its negative charge, compactness, and ability to engage in π-bonding. Among the most important cyanide coordination compounds are the potassium ferrocyanide and the pigment Prussian blue , which are both essentially nontoxic ...

  8. Strong electrolyte - Wikipedia

    en.wikipedia.org/wiki/Strong_electrolyte

    In chemistry, a strong electrolyte is a solute that completely, or almost completely, ionizes or dissociates in a solution. These ions are good conductors of electric current in the solution. Originally, a "strong electrolyte" was defined as a chemical compound that, when in aqueous solution , is a good conductor of electricity.

  9. Protonated hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Protonated_hydrogen_cyanide

    According to the database at astrochemistry.net, the most advanced chemical models of HCNH + include 71 total formation reactions and 21 total destruction reactions. Of these, however, only a handful dominate the overall formation and destruction. [13] In the case of formation, the 7 dominant reactions are: H + 3 + HCN → HCNH + + H 2 H + 3 ...