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  2. Hydrogen isocyanide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_isocyanide

    Hydrogen isocyanide (HNC) is a linear triatomic molecule with C ∞v point group symmetry.It is a zwitterion and an isomer of hydrogen cyanide (HCN). [2] Both HNC and HCN have large, similar dipole moments, with μ HNC = 3.05 Debye and μ HCN = 2.98 Debye respectively. [3]

  3. Hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_cyanide

    Hydrogen cyanide is a linear molecule, with a triple bond between carbon and nitrogen.The tautomer of HCN is HNC, hydrogen isocyanide. [citation needed]HCN has a faint bitter almond-like odor that some people are unable to detect owing to a recessive genetic trait. [12]

  4. Isocyanic acid - Wikipedia

    en.wikipedia.org/wiki/Isocyanic_acid

    The acceptor properties of HNCO are compared with other Lewis acid in the ECW model. Low-temperature photolysis of solids containing HNCO creates the tautomer cyanic acid H−O−C≡N, also called hydrogen cyanate. [15] Pure cyanic acid has not been isolated, and isocyanic acid is the predominant form in all solvents. [2]

  5. Isocyanide - Wikipedia

    en.wikipedia.org/wiki/Isocyanide

    In the carbylamine reaction (also known as the Hofmann isocyanide synthesis) alkali base reacts with chloroform to produce dichlorocarbene. The carbene then converts primary amines to isocyanides. Illustrative is the synthesis of tert -butyl isocyanide from tert -butylamine in the presence of catalytic amount of the phase transfer catalyst ...

  6. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    Acetic acid is commonly used for this purpose, in a procedure originally described by Lapworth. [7] Conjugative hydrocyanation was used to prepare the steroidal D ring. [7] Diastereoselectivity is generally high in these addition reactions, and the resulting β-cyano carbonyl compounds can be converted to a number of steroidal products.

  7. 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.

  8. Cyanide - Wikipedia

    en.wikipedia.org/wiki/Cyanide

    The most hazardous compound is hydrogen cyanide, which is a gas and kills by inhalation. For this reason, working with hydrogen cyanide requires wearing an air respirator supplied by an external oxygen source. [11] Hydrogen cyanide is produced by adding acid to a solution containing a cyanide salt.

  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 ...