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  2. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene is a fundamental ligand in transition metal alkene complexes. One of the first organometallic compounds, Zeise's salt is a complex of ethylene. Useful reagents containing ethylene include Pt(PPh 3) 2 (C 2 H 4) and Rh 2 Cl 2 (C 2 H 4) 4. The Rh-catalysed hydroformylation of ethylene is conducted on an industrial scale to provide ...

  3. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    In organic chemistry, a vinyl group (abbr. Vi; [1] IUPAC name: ethenyl group [2]) is a functional group with the formula −CH=CH 2. It is the ethylene (IUPAC name: ethene) molecule (H 2 C=CH 2) with one fewer hydrogen atom. The name is also used for any compound containing that group, namely R−CH=CH 2 where R is any other group of atoms.

  4. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The simplest alkene, ethylene (C 2 H 4) (or "ethene" in the IUPAC nomenclature) is the organic compound produced on the largest scale industrially. [5] Aromatic compounds are often drawn as cyclic alkenes, however their structure and properties are sufficiently distinct that they are not classified as alkenes or olefins. [3]

  5. Vinylene group - Wikipedia

    en.wikipedia.org/wiki/Vinylene_group

    In chemistry, vinylene (also ethenylene or 1,2-ethenediyl) [1] is a divalent functional group (a part of a molecule) [2] with formula −CH=CH−; [3] namely, two carbons, each connected to the other by a double bond, to an hydrogen atom by a single bond, and to the rest of the molecule by another single bond.

  6. Ethane - Wikipedia

    en.wikipedia.org/wiki/Ethane

    2 C 2 H 6 + 7 O 2 → 4 CO 2 + 6 H 2 O + 3120 kJ. Combustion may also occur without an excess of oxygen, yielding carbon monoxide, acetaldehyde, methane, methanol, and ethanol. At higher temperatures, especially in the range 600–900 °C (1,112–1,652 °F), ethylene is a significant product: 2 C 2 H 6 + O 22 C 2 H 4 + 2 H 2 O

  7. (E)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(E)-Stilbene

    (E)-Stilbene, commonly known as trans-stilbene, is an organic compound represented by the condensed structural formula C 6 H 5 CH=CHC 6 H 5.Classified as a diarylethene, it features a central ethylene moiety with one phenyl group substituent on each end of the carbon–carbon double bond.

  8. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    [2] [17] The Brønsted–Lowry acidbase theory was published in the same year. The two theories are distinct but complementary. A Lewis base is also a Brønsted–Lowry base, but a Lewis acid does not need to be a Brønsted–Lowry acid. The classification into hard and soft acids and bases (HSAB theory) followed in 1963. The strength of ...

  9. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    In ethylene each carbon atom has three sp 2 orbitals and one p-orbital. The three sp 2 orbitals lie in a plane with ~120° angles. The p-orbital is perpendicular to this plane. When the carbon atoms approach each other, two of the sp 2 orbitals overlap to form a sigma bond.