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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. 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.

  4. CRC Handbook of Chemistry and Physics - Wikipedia

    en.wikipedia.org/wiki/CRC_Handbook_of_Chemistry...

    9780367417246 (101st ed.) Website. https://hbcp.chemnetbase.com. The CRC Handbook of Chemistry and Physics is a comprehensive one-volume reference resource for science research. First published in 1914, it is currently (as of 2023) in its 104th edition, published in 2023. It is known colloquially among chemists as the "Rubber Bible", as CRC ...

  5. Buckminsterfullerene - Wikipedia

    en.wikipedia.org/wiki/Buckminsterfullerene

    Buckminsterfullerene is a type of fullerene with the formula C 60. It has a cage-like fused-ring structure (truncated icosahedron) made of twenty hexagons and twelve pentagons, and resembles a football. Each of its 60 carbon atoms is bonded to its three neighbors.

  6. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Cycloalkane. Ball-and-stick model of cyclobutane. 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 ...

  7. Conformational isomerism - Wikipedia

    en.wikipedia.org/wiki/Conformational_isomerism

    Conformational isomerism. Rotation about single bond of butane to interconvert one conformation to another. The gauche conformation on the right is a conformer, while the eclipsed conformation on the left is a transition state between conformers. Above: Newman projection; below: depiction of spatial orientation.

  8. Alicyclic compound - Wikipedia

    en.wikipedia.org/wiki/Alicyclic_compound

    The simplest alicyclic compounds are the monocyclic cycloalkanes: cyclopropane, cyclobutane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, and so on. Bicyclic alkanes include bicycloundecane, decalin, and housane. Polycyclic alkanes include cubane, basketane, and tetrahedrane. Spiro compounds have two or more rings that are connected ...

  9. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    A Newman projection is a drawing that helps visualize the 3-dimensional structure of a molecule. [1] This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes. A Newman projection visualizes the conformation of a chemical bond from front to back, with the front atom ...