enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Ethenone - Wikipedia

    en.wikipedia.org/wiki/Ethenone

    CH 3 CO 2 H → CH 2 =C=O + H 2 O. It has also been produced on a laboratory scale by the thermolysis of acetone at 600–700 °C. [9] [10] CH 3 COCH 3 →CH 2 =C=O + CH 4. This reaction is called the Schmidlin ketene synthesis. [11] On a laboratory scale it can be produced by the thermal decomposition of Meldrum's acid at temperatures greater ...

  3. 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.

  4. Cyclohexanethiol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanethiol

    C 6 H 12 S: Molar mass: 116.22 g·mol −1 Appearance Colorless liquid Density: 0.95 g/cm 3: Boiling point: 158 to 160 °C (316 to 320 °F; 431 to 433 K) Solubility ...

  5. 1,4-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,4-Cyclohexanedione

    1,4-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. This white solid is one of the three isomeric cyclohexanediones . This particular diketone is used as a building block in the synthesis of more complex molecules.

  6. Cyclohexenone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexenone

    Cyclohexenone is an organic compound which is a versatile intermediate used in the synthesis of a variety of chemical products such as pharmaceuticals and fragrances. [2] It is colorless liquid, but commercial samples are often yellow.

  7. Ethanol (data page) - Wikipedia

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

    of fusion, Δ fus H o +4.9 kJ/mol Std entropy change of fusion, Δ fus S o +31 J/(mol·K) Std enthalpy change of vaporization, Δ vap H o +42.3 ± 0.4 kJ/mol [4] Std entropy change of vaporization, Δ vap S o: 109.67 J/(mol·K) Molal freezing point constant: −1.99 °C kg/mol Solid properties Std enthalpy change of formation, Δ f H o solid ...

  8. Ethylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Ethylcyclohexane

    Ethylcyclohexane is an organic compound with the formula C 6 H 11 C 2 H 5. The molecule consists of an ethyl group attached to a cyclohexane ring. It is a typical naphthene in petroleum. It can be produced by hydrogenation of ethylbenzene and by hydrodeoxygenation of lignin. [2]

  9. 1,3-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,3-Cyclohexanedione

    1,3-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. It is one of three isomeric cyclohexanediones . It is a colorless compound that occurs naturally.