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  2. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    IUPAC nomenclature has extensive rules to cover the naming of cyclic structures, both as core structures, and as substituents appended to alicyclic structures. [citation needed] The term macrocycle is used when a ring-containing compound has a ring of 12 or more atoms. [6] [7] The term polycyclic is used when more than one ring appears in a ...

  3. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    The strain energy of a cycloalkane is the increase in energy caused by the compound's geometry, and is calculated by comparing the experimental standard enthalpy change of combustion of the cycloalkane with the value calculated using average bond energies. Molecular mechanics calculations are well suited to identify the many conformations ...

  4. trans-Cyclooctene - Wikipedia

    en.wikipedia.org/wiki/Trans-Cyclooctene

    trans-Cyclooctene is a cyclic hydrocarbon with the formula [–(CH 2) 6 CH=CH–], where the two C–C single bonds adjacent to the double bond are on opposite sides of the latter's plane. It is a colorless liquid with a disagreeable odor.

  5. Polycyclic aromatic hydrocarbon - Wikipedia

    en.wikipedia.org/.../Polycyclic_aromatic_hydrocarbon

    A Polycyclic aromatic hydrocarbon (PAH) is a class of organic compounds that is composed of multiple aromatic rings.Most are produced by the incomplete combustion of organic matter— by engine exhaust fumes, tobacco, incinerators, in roasted meats and cereals, [1] or when biomass burns at lower temperatures as in forest fires.

  6. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    In organic chemistry, a cycloalkene or cycloolefin is a type of alkene hydrocarbon which contains a closed ring of carbon atoms and either one or more double bonds, but has no aromatic character. Some cycloalkenes, such as cyclobutene and cyclopentene , can be used as monomers to produce polymer chains. [ 1 ]

  7. Catalytic reforming - Wikipedia

    en.wikipedia.org/wiki/Catalytic_reforming

    Catalytic reforming is a chemical process used to convert naphthas from crude oil into liquid products called reformates, which are premium "blending stocks" for high-octane gasoline. The process converts low-octane linear hydrocarbons (paraffins) into branched alkanes (isoparaffins) and cyclic naphthenes , which are then partially ...

  8. Siloxane - Wikipedia

    en.wikipedia.org/wiki/Siloxane

    Unlike dimethicones, which are linear siloxanes that do not evaporate, cyclomethicones are cyclic: both groups consist of a backbone of [(CH 3) 2 SiO] n. They are used in many cosmetic products including deodorants and antiperspirants which need to coat the skin but not remain tacky afterward. [8] Dow is a major producer of cyclomethicones. [9]

  9. Quadricyclane - Wikipedia

    en.wikipedia.org/wiki/Quadricyclane

    Quadricyclane is a strained, multi-cyclic hydrocarbon with the formula CH 2 (CH) 6. A white volatile colorless liquid, it is highly strained molecule (78.7 kcal/mol). Isomerization of quadricyclane proceeds slowly at low temperatures. [1] Because of quadricyclane's strained structure and thermal stability, it has been studied extensively.