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  2. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    The cyclohexanone–cyclohexanol mixture, called " KA oil ", is a raw material for adipic acid and caprolactam, precursors to nylon. Several million kilograms of cyclohexanone and cyclohexanol are produced annually. [9] It is used as a solvent in some brands of correction fluid. Cyclohexane is sometimes used as a non-polar organic solvent ...

  3. Sugarcane - Wikipedia

    en.wikipedia.org/wiki/Sugarcane

    Sugarcane or sugar cane is a species of tall, perennial grass (in the genus Saccharum, tribe Andropogoneae) that is used for sugar production. The plants are 2–6 m (6–20 ft) tall with stout, jointed, fibrous stalks that are rich in sucrose, [1] which accumulates in the stalk internodes. Sugarcanes belong to the grass family, Poaceae, an ...

  4. Cyclohexane (data page) - Wikipedia

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

    184.0. 228.4. —. —. Table data obtained from CRC Handbook of Chemistry and Physics 44th ed. The " (s)" annotation indicates equilibrium temperature of vapor over solid. Otherwise value is equilibrium temperature of vapor over liquid. log10 of Cyclohexane vapor pressure. Uses formula: obtained from CHERIC [5]

  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. Squalane - Wikipedia

    en.wikipedia.org/wiki/Squalane

    Squalane is the organic compound with the formula ( (CH3)2CH (CH2)3CH (CH3) (CH2)3(CH2)3CH (CH3) (CH2)2)2. A colorless hydrocarbon, it is the hydrogenated derivative of squalene, although commercial samples are derived from nature. [3] In contrast to squalene, due to the complete saturation of squalane, it is not subject to auto-oxidation.

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    IUPAC nomenclature of organic chemistry. In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended [1][2] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). [3]

  8. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Aliphatic compound. In organic chemistry, hydrocarbons (compounds composed solely of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (/ ˌælɪˈfætɪk /; G. aleiphar, fat, oil). Aliphatic compounds can be saturated (in which all the C-C bonds are single requiring the structure to be completed, or ...

  9. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    Aromatization. Aromatization is a chemical reaction in which an aromatic system is formed from a single nonaromatic precursor. Typically aromatization is achieved by dehydrogenation of existing cyclic compounds, illustrated by the conversion of cyclohexane into benzene. Aromatization includes the formation of heterocyclic systems.