When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    [1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.

  3. Protonated hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Protonated_hydrogen_cyanide

    Since the initial detection, HCNH + has also been observed in TMC-1 [15] [16] as well as DR 21(OH) [15]. [17] The initial detection toward Sgr B2 has also been confirmed. [ 15 ] [ 18 ] All 3 of these sources are dense molecular clouds, and to date HCNH + has not been detected in diffuse interstellar material.

  4. 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).

  5. Brønsted–Lowry acid–base theory - Wikipedia

    en.wikipedia.org/wiki/Brønsted–Lowry_acid...

    In the same year that Brønsted and Lowry published their theory, G. N. Lewis created an alternative theory of acid–base reactions. The Lewis theory is based on electronic structure. A Lewis base is a compound that can give an electron pair to a Lewis acid, a compound that can accept an electron pair.

  6. Gilbert N. Lewis - Wikipedia

    en.wikipedia.org/wiki/Gilbert_N._Lewis

    Gilbert Newton Lewis ForMemRS [1] (October 23 [2] [3] [4] or October 25, 1875 – March 23, 1946) [1] [5] [6] was an American physical chemist and a dean of the college of chemistry at University of California, Berkeley.

  7. 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:

  8. 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]

  9. Cyano radical - Wikipedia

    en.wikipedia.org/wiki/Cyano_radical

    Bonding in the cyano radical can be described as a combination of two resonance structures: the structure with the unpaired electron on the carbon is the minor contributor, while the structure with the unpaired electron on the nitrogen (the isocyano radical) is the major contributor.