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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 (formerly known as prussic acid) is a chemical compound with the formula HCN and structural formula H−C≡N.It is a highly toxic and flammable liquid that boils slightly above room temperature, at 25.6 °C (78.1 °F).

  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. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    The number of electron pairs in the valence shell of a central atom is determined after drawing the Lewis structure of the molecule, and expanding it to show all bonding groups and lone pairs of electrons. [1]: 410–417 In VSEPR theory, a double bond or triple bond is treated as a single bonding group. [1]

  6. Formal charge - Wikipedia

    en.wikipedia.org/wiki/Formal_charge

    Formal charges in ozone and the nitrate anion. In chemistry, a formal charge (F.C. or q*), in the covalent view of chemical bonding, is the hypothetical charge assigned to an atom in a molecule, assuming that electrons in all chemical bonds are shared equally between atoms, regardless of relative electronegativity.

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    The search engine that helps you find exactly what you're looking for. Find the most relevant information, video, images, and answers from all across the Web.

  8. Cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin

    In the laboratory, this liquid serves as a source of HCN, which is inconveniently volatile. [4] Thus, acetone cyanohydrin can be used for the preparation of other cyanohydrins, for the transformation of HCN to Michael acceptors, and for the formylation of arenes. Treatment of this cyanohydrin with lithium hydride affords anhydrous lithium cyanide:

  9. Gattermann reaction - Wikipedia

    en.wikipedia.org/wiki/Gattermann_reaction

    The reaction can be simplified by replacing the HCN/AlCl 3 combination with zinc cyanide. [4] Although it is also highly toxic, Zn(CN) 2 is a solid, making it safer to work with than gaseous HCN. [5] The Zn(CN) 2 reacts with the HCl to form the key HCN reactant and Zn(Cl) 2 that serves as the Lewis-acid catalyst in-situ.