enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    In organic and physical organic chemistry, Clar's rule is an empirical rule that relates the chemical stability of a molecule to its aromaticity.It was introduced in 1972 by the Austrian organic chemist Erich Clar in his book The Aromatic Sextet.

  3. Covalent bond - Wikipedia

    en.wikipedia.org/wiki/Covalent_bond

    In organic chemistry, covalent bonding is much more common than ionic bonding. Covalent bonding also includes many kinds of interactions, including σ-bonding, π-bonding, metal-to-metal bonding, agostic interactions, bent bonds, three-center two-electron bonds and three-center four-electron bonds. [2] [3] The term covalent bond dates from 1939 ...

  4. Bridging ligand - Wikipedia

    en.wikipedia.org/wiki/Bridging_ligand

    For doubly bridging (μ 2-) ligands, two limiting representation are 4-electron and 2-electron bonding interactions. These cases are illustrated in main group chemistry by [Me 2 Al(μ 2-Cl)] 2 and [Me 2 Al(μ 2-Me)] 2. Complicating this analysis is the possibility of metal–metal bonding.

  5. Functionality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Functionality_(Chemistry)

    However, IUPAC definition and the use of the term in organic chemistry differ with respect to the functionality of a double bond. [6] [9] In polymer chemistry, a double bond possesses a functionality of two (because two points of contact for further polymer chains are present, on each of the two adjacent carbon atoms), while in organic ...

  6. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Each bond consists of a pair of electrons, so if t is the total number of electrons to be placed and n is the number of single bonds just drawn, t−2n electrons remain to be placed. These are temporarily drawn as dots, one per electron, to a maximum of eight per atom (two in the case of hydrogen), minus two for each bond.

  7. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–carbon_bond

    Carbon is one of the few elements that can form long chains of its own atoms, a property called catenation.This coupled with the strength of the carbon–carbon bond gives rise to an enormous number of molecular forms, many of which are important structural elements of life, so carbon compounds have their own field of study: organic chemistry.

  8. Organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Organic_chemistry

    Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms. [1]

  9. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    Other common double bonds are found in azo compounds (N=N), imines (C=N), and sulfoxides (S=O). In a skeletal formula, a double bond is drawn as two parallel lines (=) between the two connected atoms; typographically, the equals sign is used for this. [1] [2] Double bonds were introduced in chemical notation by Russian chemist Alexander Butlerov.