enow.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. Formic acid - Wikipedia

    en.wikipedia.org/wiki/Formic_acid

    2 hc(o)nh 2 + 2h 2 o + h 2 so 4 → 2hco 2 h + (nh 4) 2 so 4 A disadvantage of this approach is the need to dispose of the ammonium sulfate byproduct. This problem has led some manufacturers to develop energy-efficient methods of separating formic acid from the excess water used in direct hydrolysis.

  4. CH2O2 - Wikipedia

    en.wikipedia.org/wiki/CH2O2

    This page was last edited on 29 September 2022, at 20:23 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. Linnett double-quartet theory - Wikipedia

    en.wikipedia.org/wiki/Linnett_Double-Quartet_Theory

    The cornerstone of classical bonding theories is the Lewis structure, published by G. N. Lewis in 1916 and continuing to be widely taught and disseminated to this day. [3] In this theory, the electrons in bonds are believed to pair up, forming electron pairs which result in the binding of nuclei .

  6. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    BF 3 + F − → BF − 4. In this adduct, all four fluoride centres (or more accurately, ligands) are equivalent. BF 3 + OMe 2 → BF 3 OMe 2. Both BF 4 − and BF 3 OMe 2 are Lewis base adducts of boron trifluoride. Many adducts violate the octet rule, such as the triiodide anion: I 2 + I − → I − 3

  7. C2H4O2 - Wikipedia

    en.wikipedia.org/wiki/C2H4O2

    C 2 H 4 O 2 may refer to: Compounds sharing the molecular formula: Acetic acid; Dihydroxyethene isomers: 1,1-Dihydroxyethene (E)-1,2-Dihydroxyethene (Z)-1,2 ...

  8. Methyl formate - Wikipedia

    en.wikipedia.org/wiki/Methyl_formate

    In the laboratory, methyl formate can be produced by the condensation reaction of methanol and formic acid, as follows: . HCOOH + CH 3 OH → HCOOCH 3 + H 2 O. Industrial methyl formate, however, is usually produced by the combination of methanol and carbon monoxide (carbonylation) in the presence of a strong base, such as sodium methoxide: [4]

  9. Dioxirane - Wikipedia

    en.wikipedia.org/wiki/Dioxirane

    In chemistry, dioxirane (systematically named dioxacyclopropane, also known as methylene peroxide or peroxymethane) is an organic compound with formula CH 2 O 2.The molecule consists of a ring with one methylene and two oxygen atoms.