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  2. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5] Cyclohexyl (C 6 H 11) is the alkyl substituent of cyclohexane and is ...

  3. Cycloalkyne - Wikipedia

    en.wikipedia.org/wiki/Cycloalkyne

    Cycloalkyne. In organic chemistry, a cycloalkyne is the cyclic analog of an alkyne (−C≡C−). A cycloalkyne consists of a closed ring of carbon atoms containing one or more triple bonds. Cycloalkynes have a general formula CnH2n−4. Because of the linear nature of the C−C≡C−C alkyne unit, cycloalkynes can be highly strained and can ...

  4. Cyclohexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_(data_page)

    Critical point. 554 K (281 °C), 4070 kPa. Std enthalpy change of fusion, Δ fusH o. 2.68 kJ/mol crystal I → liquid. Std entropy change of fusion, Δ fusS o. 9.57 J/ (mol·K) crystal I → liquid. Std enthalpy change of vaporization, Δ vapH o. 32 kJ/mol. Std entropy change of vaporization, Δ vapS o.

  5. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    A cyclohexane molecule in chair conformation. Hydrogen atoms in axial positions are shown in red, while those in equatorial positions are in blue. Cyclohexane conformations are any of several three-dimensional shapes adopted by molecules of cyclohexane. Because many compounds feature structurally similar six-membered rings, the structure and ...

  6. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is most stable in a half-chair conformation, [11] unlike the preference for a chair form of cyclohexane. One basis for the cyclohexane conformational preference for a chair is that it allows each bond of the ring to adopt a staggered conformation. For cyclohexene, however, the alkene is planar, equivalent to an eclipsed conformation ...

  7. Robinson annulation - Wikipedia

    en.wikipedia.org/wiki/Robinson_annulation

    RXNO:0000380. The Robinson annulation is a chemical reaction used in organic chemistry for ring formation. It was discovered by Robert Robinson in 1935 as a method to create a six membered ring by forming three new carbon–carbon bonds. [1] The method uses a ketone and a methyl vinyl ketone to form an α,β-unsaturated ketone in a cyclohexane ...

  8. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    A cyclic compound(or ring compound) is a term for a compoundin the field of chemistryin which one or more series of atoms in the compound is connected to form a ring. Rings may vary in size from three to many atoms, and include examples where all the atoms are carbon (i.e., are carbocycles), none of the atoms are carbon (inorganic cyclic ...

  9. Cahn–Ingold–Prelog priority rules - Wikipedia

    en.wikipedia.org/wiki/Cahn–Ingold–Prelog...

    For double bonded molecules, Cahn–Ingold–Prelog priority rules (CIP rules) are followed to determine the priority of substituents of the double bond. If both of the high priority groups are on the same side of the double bond (cis configuration), then the stereoisomer is assigned the configuration Z (zusammen, German word meaning "together").