When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  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

    These species usually are easily separated from liquid- or gas-phase reaction products. [2] Isocyanic acid reacts with amines to give ureas (carbamides): HNCO + RNH 2 → RNHC(O)NH 2. This reaction is called carbamylation. Excess isocyanic acid can react with the ureas to give allophanates. [2]

  5. Water-reactive substances - Wikipedia

    en.wikipedia.org/wiki/Water-reactive_substances

    Magnesium has a mild reaction with cold water. The reaction is short-lived because the magnesium hydroxide layer formed on the magnesium is almost insoluble in water and prevents further reaction. Mg(s) + 2H 2 O(l) Mg(OH) 2 (s) + H 2 (g) [11] A metal reacting with cold water will produce a metal hydroxide and hydrogen gas.

  6. Cyanate - Wikipedia

    en.wikipedia.org/wiki/Cyanate

    A similar reaction is used to make potassium cyanate. Cyanates are produced when cyanides are oxidized. Use of this fact is made in cyanide decontamination processes where oxidants such as permanganate and hydrogen peroxide are used to convert toxic cyanide into less-toxic cyanate.

  7. 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 ...

  8. Cyanide - Wikipedia

    en.wikipedia.org/wiki/Cyanide

    Cyanide is unstable in water, but the reaction is slow until about 170 °C. It undergoes hydrolysis to give ammonia and formate, which are far less toxic than cyanide: [14] CN − + 2 H 2 O → HCO − 2 + NH 3. Cyanide hydrolase is an enzyme that catalyzes this reaction.

  9. 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.