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  2. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    2 c 6 h 12 + o 22 c 6 h 11 oh This process coforms cyclohexanone , and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid . The oxidation involves radicals and the intermediacy of the hydroperoxide C 6 H 11 O 2 H. Alternatively, cyclohexanol can be produced by the hydrogenation of phenol :

  3. Ethenone - Wikipedia

    en.wikipedia.org/wiki/Ethenone

    Ethenone reacts with methanal in the presence of catalysts such as Lewis acids (AlCl 3, ZnCl 2 or BF 3) to give β-propiolactone. [21] The technically most significant use of ethenone is the synthesis of sorbic acid by reaction with 2-butenal (crotonaldehyde) in toluene at about 50 °C in the presence of zinc salts of long-chain carboxylic acids.

  4. Cyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone

    Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.

  5. Ethanol (data page) - Wikipedia

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

    Phase behavior Triple point: 150 K (−123 °C), 0.00043 Pa Critical point: 514 K (241 °C), 63 bar Std enthalpy change of fusion, Δ fus H o +4.9 kJ/mol

  6. Molar volume - Wikipedia

    en.wikipedia.org/wiki/Molar_volume

    The ideal gas equation can be rearranged to give an expression for the molar volume of an ideal gas: = = Hence, for a given temperature and pressure, the molar volume is the same for all ideal gases and is based on the gas constant: R = 8.314 462 618 153 24 m 3 ⋅Pa⋅K −1 ⋅mol −1, or about 8.205 736 608 095 96 × 10 −5 m 3 ⋅atm⋅K ...

  7. 1-Ethynylcyclohexanol - Wikipedia

    en.wikipedia.org/wiki/1-Ethynylcyclohexanol

    1-Ethynylcyclohexanol (ECX) is an alkynyl alcohol derivative which is both a synthetic precursor to, and an active metabolite of the tranquilizer ethinamate, and has similar sedative, anticonvulsant and muscle relaxant effects. It has been sold as a designer drug, first being identified in the UK in March 2012. [1] [2] [3] [4]

  8. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    Cyclohexylmethanol is an organic compound with the formula C 6 H 11 −CH 2 −OH. It is a cyclohexane ring functionalized with an alcohol , specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow.

  9. Cyclohexanethiol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanethiol

    [1] It is produced industrially by the hydrogenation of cyclohexanone in the presence of hydrogen sulfide over a metal sulfide catalyst: C 6 H 10 O + H 2 S + H 2 → C 6 H 11 SH + H 2 O. It is also obtained by the addition of hydrogen sulfide to cyclohexene in the presence of nickel sulfide. [2]