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  2. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    Subsequent binding of the alkene gives the intermediate M(H)(CN)L n (alkene), which then undergoes migratory insertion to give an alkylmetal cyanide. The cycle is completed by the reductive elimination of the nitrile. Lewis acids, such as triphenylboron (B(C 6 H 5) 3), induce reductive elimination of the nitrile product, increasing rates. [1]

  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. 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.

  5. Gilbert N. Lewis - Wikipedia

    en.wikipedia.org/wiki/Gilbert_N._Lewis

    Lewis had been working on an experiment with liquid hydrogen cyanide, and deadly fumes from a broken line had leaked into the laboratory. The coroner ruled that the cause of death was coronary artery disease , because of a lack of any signs of cyanosis, [ 34 ] but some believe that it may have been a suicide.

  6. 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.

  7. Formylation - Wikipedia

    en.wikipedia.org/wiki/Formylation

    Carbon monoxide and hydrochloric acid in the Gattermann-Koch reaction; Cyanides in the Gattermann reaction. This method synthesizes aromatic aldehydes using hydrogen chloride and hydrogen cyanide (or another metallic cyanide as such zinc cyanide) in the presence of Lewis acid catalysts: Chloroform in the Reimer-Tiemann reaction

  8. 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]

  9. Andrussow process - Wikipedia

    en.wikipedia.org/wiki/Andrussow_process

    The Andrussow process is the dominant industrial process for the production of hydrogen cyanide. [1] It involves the reaction of methane, ammonia, and oxygen. The process is catalyzed by a platinum-rhodium alloy. [2] 2 CH 4 + 2 NH 3 + 3 O 2 → 2 HCN + 6 H 2 O