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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. 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.

  4. Hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_cyanide

    A hydrogen cyanide concentration of 100–200 ppm in breathing air will kill a human within 10 to 60 minutes. [68] A hydrogen cyanide concentration of 2000 ppm (about 2380 mg/m 3) will kill a human in about one minute. [68] The toxic effect is caused by the action of the cyanide ion, which halts cellular respiration.

  5. Protonated hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Protonated_hydrogen_cyanide

    Models of Titan's atmosphere had predicted that HCNH + would be the dominant ion present, and a strong peak in the mass spectrum at ⁠ m / z ⁠ = 28 seems to support this theory. In 1997, observations were made of the long-period comet Hale–Bopp in an attempt to find HCNH + , [ 20 ] but it was not detected.

  6. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  7. Cyanogen bromide - Wikipedia

    en.wikipedia.org/wiki/Cyanogen_bromide

    If the sulfur in cysteine attacked cyanogen bromide, the bromide ion would deprotonate the cyanide adduct, leaving the sulfur uncharged and the beta carbon of the cysteine not electrophilic. The strongest electrophile would then be the cyanide carbon, which, if attacked by water, would yield cyanic acid and the original cysteine.

  8. Cyanate - Wikipedia

    en.wikipedia.org/wiki/Cyanate

    Any salt containing the ion, such as ammonium cyanate, is called a cyanate. The cyanate ion is an isomer of the much-less-stable fulminate anion, CNO − or [C − ≡N + −O −]. [1] The cyanate ion is an ambidentate ligand, forming complexes with a metal ion in which either the nitrogen or oxygen atom may be the electron-pair donor.

  9. Cyanonickelate - Wikipedia

    en.wikipedia.org/wiki/Cyanonickelate

    The ion has cyanide groups arranged in a square around the central nickel ion. The symmetry of the ion is D 4h. The distance from the nickel atom to the carbon is 1.87 Å, and the carbon-nitrogen distance is 1.16 Å. [1] In their crystals, the tetracyanonickelate(II) anions are often arranged in a columnar structure (e.g. in K 2 [Ni(CN) 4] [2]).