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  2. Cyanide - Wikipedia

    en.wikipedia.org/wiki/Cyanide

    Cyanide is quantified by potentiometric titration, a method widely used in gold mining. It can also be determined by titration with silver ion. Some analyses begin with an air-purge of an acidified boiling solution, sweeping the vapors into a basic absorber solution. The cyanide salt absorbed in the basic solution is then analyzed. [47]

  3. Hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_cyanide

    The word cyanide for the radical in hydrogen cyanide was derived from its French equivalent, cyanure, which Gay-Lussac constructed from the Ancient Greek word κύανος for dark blue enamel or lapis lazuli, again owing to the chemical’s derivation from Prussian blue. Incidentally, the Greek word is also the root of the English color name cyan.

  4. Cyanogen - Wikipedia

    en.wikipedia.org/wiki/Cyanogen

    Cyanogen is typically generated from cyanide compounds. One laboratory method entails thermal decomposition of mercuric cyanide: . 2 Hg(CN) 2 → (CN) 2 + Hg 2 (CN) 2 Or, one can combine solutions of copper(II) salts (such as copper(II) sulfate) with cyanides; an unstable copper(II) cyanide is formed which rapidly decomposes into copper(I) cyanide and cyanogen.

  5. Potassium cyanide - Wikipedia

    en.wikipedia.org/wiki/Potassium_cyanide

    Potassium cyanide is a compound with the formula KCN. It is a colorless salt, similar in appearance to sugar , that is highly soluble in water. Most KCN is used in gold mining , organic synthesis , and electroplating .

  6. Formyl cyanide - Wikipedia

    en.wikipedia.org/wiki/Formyl_cyanide

    Formyl cyanide is a simple organic compound with the formula HCOCN and structure HC(=O)−C≡N. It is simultaneously a nitrile (R−C≡N) and an aldehyde (R−CH=O). Formyl cyanide is the simplest member of the acyl cyanide family. It is known to occur in space in the Sgr B2 molecular cloud. [1]

  7. Acetyl cyanide - Wikipedia

    en.wikipedia.org/wiki/Acetyl_cyanide

    Aldol condensation can occur when acetyl cyanide reacts with (Z)-but-2-enal to form (2E,4E)-hexa-2,4-dienoyl cyanide: The photochemical and thermal reactions of acetyl cyanide have been extensively studied. For example, formyl cyanide does not undergo unimolecular decomposition to HCN and CO spontaneously. However, acetyl cyanide, also a member ...

  8. Copper (I) cyanide - Wikipedia

    en.wikipedia.org/wiki/Copper(I)_cyanide

    Copper cyanide is a coordination polymer.It exists in two polymorphs both of which contain -[Cu-CN]- chains made from linear copper(I) centres linked by cyanide bridges.In the high-temperature polymorph, HT-CuCN, which is isostructural with AgCN, the linear chains pack on a hexagonal lattice and adjacent chains are off set by +/- 1/3 c, Figure 1. [5]

  9. Cyanogen iodide - Wikipedia

    en.wikipedia.org/wiki/Cyanogen_iodide

    Cyanogen iodide may cause convulsions, paralysis and death from respiratory failure. It is a strong irritant and may cause burns to the eyes and skin if contacted. If cyanogen iodide is heated enough to undergo complete decomposition, it may releases toxic fumes of nitrogen oxides, cyanide and iodide. A fire may cause the release of poisonous gas.