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  2. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    The oxidation of primary alcohols to carboxylic acids can be carried out using a variety of reagents, but O 2 /air and nitric acid dominate as the oxidants on a commercial scale. Large scale oxidations of this type are used for the conversion of cyclohexanol alone or as a mixture with cyclohexanone to adipic acid. Similarly cyclododecanol is ...

  3. Ethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_sulfate

    If the temperature exceeds 140 °C, the ethyl sulfate product tends to react with residual ethanol starting material, producing diethyl ether. If the temperature exceeds 170 °C in a considerable excess of sulfuric acid, the ethyl sulfate breaks down into ethylene and sulfuric acid. [12] [13]

  4. Enthalpy change of solution - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_change_of_solution

    The equilibrium, between the gas as a separate phase and the gas in solution, will by Le Châtelier's principle shift to favour the gas going into solution as the temperature is decreased (decreasing the temperature increases the solubility of a gas). When a saturated solution of a gas is heated, gas comes out of the solution.

  5. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    Subsequently, this sulphate ester is hydrolyzed to regenerate sulphuric acid and release ethanol: C 2 H 5-O-SO 3 H + H 2 O → H 2 SO 4 + C 2 H 5 OH. This two step route is called the "indirect process". In the "direct process," the acid protonates the alkene, and water reacts with this incipient carbocation to give the alcohol.

  6. Ethanol (data page) - Wikipedia

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

    Heat capacity, c p: 111.46 J/(mol K) [5] Liquid properties Std enthalpy change of formation, Δ f H o liquid: −277.38 kJ/mol Standard molar entropy, S o liquid: 159.9 J/(mol K) Enthalpy of combustion, Δ c H o: −1370.7 kJ/mol Heat capacity, c p: 112.4 J/(mol K) Gas properties Std enthalpy change of formation, Δ f H o gas: −235.3 kJ/mol ...

  7. Saponification - Wikipedia

    en.wikipedia.org/wiki/Saponification

    Saponification is a process of cleaving esters into carboxylate salts and alcohols by the action of aqueous alkali.Typically aqueous sodium hydroxide solutions are used. [1] [2] It is an important type of alkaline hydrolysis.

  8. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula CH 3 CH 2 OH. It is an alcohol, with its formula also written as C 2 H 5 OH, C 2 H 6 O or EtOH, where Et stands for ethyl. Ethanol is a volatile, flammable, colorless liquid with a characteristic wine-like ...

  9. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Hydrochloric Acid: 84.8 [13] tert-Butanol: 82.5 [14] Chlorobenzene: 131.7 [15] p-chlorobenzotrifluoride: 1.34 136 –36.1 [16] MTBE: 55.2 [17] Pentane: 36.1 [18] Petroleum Ether: 35.0-60.0 [19] Cyclopentane: 49.3 [20] Isopropanol: 82.3 [21] Dichloromethane: 1.33 39.8 [22] n-Propanol: 97.2 [23] Pyridine: 115.3 [24] Dimethylacetamide: 166.1 [25 ...