When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  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.

  4. 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]

  5. 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.

  6. Jones oxidation - Wikipedia

    en.wikipedia.org/wiki/Jones_oxidation

    The reaction stoichiometry implicates the Cr(IV) species "CrO 2 OH −", which comproportionates with the chromic acid to give a Cr(V) oxide, which also functions as an oxidant for the alcohol. [ 6 ] The oxidation of the aldehydes is proposed to proceed via the formation of hemiacetal -like intermediates, which arise from the addition of the O ...

  7. 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 ...

  8. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    The scope of this reaction has been extended to reactions of carbonyls with alkyl azides R-N 3. This extension was first reported by J.H. Boyer in 1955 [9] (hence the name Boyer reaction), for example, the reaction of 3-nitrobenzaldehyde with β-azido ethanol: The Boyer reaction

  9. 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 ...