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  2. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    Indeed, the development of this important chemical concept arose historically in reference to cyclic compounds. Finally, cyclic compounds, because of the unique shapes, reactivities, properties, and bioactivities that they engender, are the majority of all molecules involved in the biochemistry, structure, and function of living organisms , and ...

  3. Group 14 hydride - Wikipedia

    en.wikipedia.org/wiki/Group_14_hydride

    Hydrocarbons also include alkenes, which contain a double bond between carbon atoms (e.g. ethylene H 2 C=CH 2), alkynes, which contain a triple bond between carbon atoms (e.g. acetylene H−C≡C−H), cyclic and branched hydrocarbons (e.g. cyclohexane C 6 H 12, limonene C 10 H 16, which is a cyclic hydrocarbon with double bonds between carbon ...

  4. Cycloalkyne - Wikipedia

    en.wikipedia.org/wiki/Cycloalkyne

    Due to the activated nature of the cyclic carbon–carbon triple bond, many alkyne addition-type reactions such as the Diels–Alder, 1,3-dipolar cycloadditions and halogenation may be performed using very mild conditions and in the absence of the catalysts frequently required to accelerate the transformation in a non-cyclic system. In addition ...

  5. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    In organic chemistry, the cycloalkanes (also called naphthenes, but distinct from naphthalene) are the monocyclic saturated hydrocarbons. [1] In other words, a cycloalkane consists only of hydrogen and carbon atoms arranged in a structure containing a single ring (possibly with side chains), and all of the carbon-carbon bonds are single.

  6. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    Clar's rule states that for a benzenoid polycyclic aromatic hydrocarbon (i.e. one with only hexagonal rings), the resonance structure with the largest number of disjoint aromatic π-sextets is the most important to characterize its chemical and physical properties. Such a resonance structure is called a Clar structure. In other words, a ...

  7. 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]

  8. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    Oil refineries are one way hydrocarbons are processed for use. Crude oil is processed in several stages to form desired hydrocarbons, used as fuel and in other products. Tank wagon 33 80 7920 362–0 with hydrocarbon gas at Bahnhof Enns (2018) The predominant use of hydrocarbons is as a combustible fuel source. Methane is the predominant ...

  9. Polycyclic aromatic hydrocarbon - Wikipedia

    en.wikipedia.org/.../Polycyclic_aromatic_hydrocarbon

    The benzenoid hydrocarbons have been defined as condensed polycyclic unsaturated fully-conjugated hydrocarbons whose molecules are essentially planar with all rings six-membered. Full conjugation means that all carbon atoms and carbon-carbon bonds must have the sp 2 structure of benzene.