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  2. Cyclohexane (data page) - Wikipedia

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

    Otherwise value is equilibrium temperature of vapor over liquid. log 10 of Cyclohexane vapor pressure. Uses formula: ...

  3. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane has two crystalline phases. The high-temperature phase I, stable between 186 K and the melting point 280 K, is a plastic crystal, which means the molecules retain some rotational degree of freedom. The low-temperature (below 186 K) phase II is ordered.

  4. 1,2,4,5-Cyclohexanetetrol - Wikipedia

    en.wikipedia.org/wiki/1,2,4,5-cyclohexanetetrol

    1,2,4,5-Cyclohexanetetrol (also named cyclohexane-1,2,4,5-tetrol, 1,2,4,5-tetrahydroxycyclohexane, or para-cyclohexanetetrol) is an organic compound whose molecule can be described as a cyclohexane with four hydroxyl (OH) groups substituted for hydrogen atoms on two non-adjacent pairs of adjacent carbon atoms. Its formula can be written C 6 H ...

  5. Trouton's rule - Wikipedia

    en.wikipedia.org/wiki/Trouton's_rule

    Enthalpies of melting and boiling for pure elements versus temperatures of transition, demonstrating Trouton's rule. In thermodynamics, Trouton's rule states that the (molar) entropy of vaporization is almost the same value, about 85–88 J/(K·mol), for various kinds of liquids at their boiling points. [1]

  6. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    Melting point: 19 °C (66 °F) [1] Boiling point: 187–188 °C (369–370 °F) [3] Solubility in water. ... It is a cyclohexane ring functionalized with an alcohol ...

  7. Cyclohexanedimethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanedimethanol

    It is a colorless low-melting solid used in the production of polyester resins. Commercial samples consist of a mixture of cis and trans isomers. It is a di-substituted derivative of cyclohexane and is classified as a diol, meaning that it has two OH functional groups. Commercial CHDM typically has a cis/trans ratio of 30:70.

  8. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    Most methylcyclohexane is extracted from petroleum but it can be also produced by catalytic hydrogenation of toluene: CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. The hydrocarbon is a minor component of automobile fuel, with its share in US gasoline varying between 0.3 and 1.7% in early 1990s [10] and 0.1 to 1% in 2011. [11]

  9. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    Melting point: −57 °C (−71 °F; 216 K) Boiling point: ... Bromocyclohexane can be prepared by the free radical bromination of cyclohexane. Safety