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  2. Jones oxidation - Wikipedia

    en.wikipedia.org/wiki/Jones_oxidation

    For oxidations to the aldehydes and ketones, two equivalents of chromic acid oxidize three equivalents of the alcohol: 2 HCrO 4 − + 3 RR'C(OH)H + 8 H + + 4 H 2 O → 2 [Cr(H 2 O) 6] 3+ + 3 RR'CO. For oxidation of primary alcohols to carboxylic acids, 4 equivalents of chromic acid oxidize 3 equivalents of the alcohol. The aldehyde is an ...

  3. Potassium dichromate - Wikipedia

    en.wikipedia.org/wiki/Potassium_dichromate

    In 2005–06, potassium dichromate was the 11th-most-prevalent allergen in patch tests (4.8%). [12] Potassium dichromate is one of the most common causes of chromium dermatitis; [13] chromium is highly likely to induce sensitization leading to dermatitis, especially of the hand and forearms, which is chronic and difficult to treat ...

  4. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  5. 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 ...

  6. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom. [ 3 ] [ 4 ] Alcohols range from the simple, like methanol and ethanol , to complex, like sugar alcohols and cholesterol .

  7. Chromyl chloride - Wikipedia

    en.wikipedia.org/wiki/Chromyl_chloride

    Chromyl chloride can be prepared by the reaction of potassium chromate or potassium dichromate with hydrogen chloride in the presence of sulfuric acid, followed by distillation. [3] [4] K 2 Cr 2 O 7 + 6 HCl → 2 CrO 2 Cl 2 + 2 KCl + 3 H 2 O. The sulfuric acid serves as the dehydration agent.

  8. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  9. Étard reaction - Wikipedia

    en.wikipedia.org/wiki/Étard_reaction

    The Étard reaction is a chemical reaction that involves the direct oxidation of an aromatic or heterocyclic bound methyl group to an aldehyde using chromyl chloride. [1] [2] [3] For example, toluene can be oxidized to benzaldehyde. It is named for the French chemist Alexandre Léon Étard (5 January 1852, Alençon – 1 May 1910).