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  2. Outline of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Outline_of_organic_chemistry

    The following outline is provided as an overview of and topical guide to organic chemistry: . Organic chemistry is the scientific study of the structure, properties, composition, reactions, and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives.

  3. Chemistry - Wikipedia

    en.wikipedia.org/wiki/Chemistry

    Chemistry is the scientific study of the properties and behavior of matter. [1] It is a physical science within the natural sciences that studies the chemical elements that make up matter and compounds made of atoms, molecules and ions: their composition, structure, properties, behavior and the changes they undergo during reactions with other substances.

  4. Methylidyne radical - Wikipedia

    en.wikipedia.org/wiki/Methylidyne_radical

    HCCo 3 (CO) 9, a metal cluster complex with a methylidyne ligand.. As an odd-electron species, CH is a radical. The ground state is a doublet (X 2 Π).The first two excited states are a quartet (with three unpaired electrons) (a 4 Σ −) and a doublet (A 2 Δ).

  5. 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]

  6. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Thus, they continue to enjoy widespread use by chemists and chemistry educators. This is especially true in the field of organic chemistry , where the traditional valence-bond model of bonding still dominates, and mechanisms are often understood in terms of curve-arrow notation superimposed upon skeletal formulae , which are shorthand versions ...

  7. Methylene (compound) - Wikipedia

    en.wikipedia.org/wiki/Methylene_(compound)

    [CH 2] 2• (X̃ 3 B 1) + H 2 O → [CH 3] • + [HO] • [CH 2] (ã 1 A 1) + H 2 O → H 2 CO + H 2 or H 3 COH. The singlet state is also more stereospecific than the triplet. [10] Methylene spontaneously autopolymerises to form various excited oligomers, the simplest of which, is the excited form of the alkene ethylene. The excited oligomers ...

  8. Organopalladium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organopalladium_chemistry

    Organopalladium chemistry is a branch of organometallic chemistry that deals with organic palladium compounds and their reactions. Palladium is often used as a catalyst in the reduction of alkenes and alkynes with hydrogen. This process involves the formation of a palladium-carbon covalent bond.

  9. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3. It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium). In IUPAC nomenclature, an acetyl group is called an ethanoyl group.