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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. 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.

  4. 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.

  5. 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.

  6. 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.

  7. Cyanation - Wikipedia

    en.wikipedia.org/wiki/Cyanation

    Deactivation of Pd(II) with excess cyanide is a common problem. [7] Palladium catalysis conditions for aryl iodides, bromides, and even chlorides have been developed: [8] Nickel-catalyzed cyanations avoid the use of precious metals, and can take advantage of benzyl cyanide or acetonitrile as a cyanide source, via reductive C-C bond cleavage: [9]

  8. Zinc cyanide - Wikipedia

    en.wikipedia.org/wiki/Zinc_cyanide

    Zinc cyanide is the inorganic compound with the formula Zn 2. It is a white solid that is used mainly for electroplating zinc but also has more specialized applications for the synthesis of organic compounds .

  9. Isocyanic acid - Wikipedia

    en.wikipedia.org/wiki/Isocyanic_acid

    Isocyanic acid, HNCO, is a Lewis acid whose free energy, enthalpy and entropy changes for its 1:1 association with a number of bases in carbon tetrachloride solution at 25 °C have been reported. [14] The acceptor properties of HNCO are compared with other Lewis acid in the ECW model.