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  2. Ethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_sulfate

    The sulfuric acid must be added dropwise or the reaction must be actively cooled because the reaction itself is highly exothermic. CH 3 CH 2 OH + H 2 SO 4 → CH 3 CH 2 OSO 3 H + H 2 O. If the temperature exceeds 140 °C, the ethyl sulfate product tends to react with residual ethanol starting material, producing diethyl ether.

  3. Solvolysis - Wikipedia

    en.wikipedia.org/wiki/Solvolysis

    An example of a solvolysis reaction is the reaction of a triglyceride with a simple alcohol such as methanol or ethanol to give the methyl or ethyl esters of the fatty acid, as well as glycerol. This reaction is more commonly known as a transesterification reaction due to the exchange of the alcohol fragments. [2]

  4. Molisch's test - Wikipedia

    en.wikipedia.org/wiki/Molisch's_test

    Molisch test (using α-napthol) indicating a positive result (see purple ring). Molisch's test is a sensitive chemical test, named after Austrian botanist Hans Molisch, for the presence of carbohydrates, based on the dehydration of the carbohydrate by sulfuric acid or hydrochloric acid to produce an aldehyde, which condenses with two molecules of a phenol (usually α-naphthol, though other ...

  5. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol is not used industrially as a precursor to ethyl halides, but the reactions are illustrative. Ethanol reacts with hydrogen halides to produce ethyl halides such as ethyl chloride and ethyl bromide via an S N 2 reaction: CH 3 CH 2 OH + HCl → CH 3 CH 2 Cl + H 2 O. HCl requires a catalyst such as zinc chloride. [116]

  6. 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.

  7. 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.

  8. Carbon snake - Wikipedia

    en.wikipedia.org/wiki/Carbon_snake

    The expansion of the mixture is the result of vaporization of water and CO 2 inside the container. The gases inflate the mixture to form a snake-like shape, and give off a burned sugar smell. [1] The granularity of the sugar can greatly affect the reaction: powdered sugar reacts very quickly but sugar cubes take longer to react. [2]

  9. Pharmacology of ethanol - Wikipedia

    en.wikipedia.org/wiki/Pharmacology_of_ethanol

    The reaction from ethanol to carbon dioxide and water proceeds in at least 11 steps in humans. C 2 H 6 O (ethanol) is converted to C 2 H 4 O (acetaldehyde), then to C 2 H 4 O 2 (acetic acid), then to acetyl-CoA. Once acetyl-CoA is formed, it is free to enter directly into the citric acid cycle (TCA) and is converted to 2 CO 2 molecules in 8 ...

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