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  2. Enol - Wikipedia

    en.wikipedia.org/wiki/Enol

    Enediols are alkenes with a hydroxyl group on each carbon of the C=C double bond. Normally such compounds are disfavored components in equilibria with acyloins. One special case is catechol, where the C=C subunit is part of an aromatic ring. In some other cases however, enediols are stabilized by flanking carbonyl groups.

  3. C2-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C2-Benzenes

    The C 2 benzenes are a class of organic aromatic compounds which contain a benzene ring and two other carbon atoms. For the hydrocarbons with no further unsaturation, there are four isomers. There are three xylenes and one ethylbenzene .

  4. Riley oxidation - Wikipedia

    en.wikipedia.org/wiki/Riley_oxidation

    The Riley oxidation is a selenium dioxide-mediated oxidation of methylene groups adjacent to carbonyls. It was first reported by Harry Lister Riley and co-workers in 1932. [ 1 ] In the decade that ensued, selenium -mediated oxidation rapidly expanded in use, and in 1939, Andre Guillemonat and co-workers disclosed the selenium dioxide-mediated ...

  5. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    The oxidation products derived from methyl are hydroxymethyl group −CH 2 OH, formyl group −CHO, and carboxyl group −COOH. For example, permanganate often converts a methyl group to a carboxyl (−COOH) group, e.g. the conversion of toluene to benzoic acid. Ultimately oxidation of methyl groups gives protons and carbon dioxide, as seen in ...

  6. Ketene - Wikipedia

    en.wikipedia.org/wiki/Ketene

    In organic chemistry, a ketene is an organic compound of the form RR'C=C=O, where R and R' are two arbitrary monovalent chemical groups (or two separate substitution sites in the same molecule). [1] The name may also refer to the specific compound ethenone H 2 C=C=O, the simplest ketene. [2] Although they are highly useful, most ketenes are ...

  7. Mesitylene - Wikipedia

    en.wikipedia.org/wiki/Mesitylene

    Mesitylene or 1,3,5-trimethylbenzene is a derivative of benzene with three methyl substituents positioned symmetrically around the ring. The other two isomeric trimethylbenzenes are 1,2,4-trimethylbenzene (pseudocumene) and 1,2,3-trimethylbenzene (hemimellitene).

  8. Selenium dioxide - Wikipedia

    en.wikipedia.org/wiki/Selenium_dioxide

    Whereas SO 2 tends to be molecular and SeO 2 is a one-dimensional chain, TeO 2 is a cross-linked polymer. [5] SeO 2 is considered an acidic oxide: it dissolves in water to form selenous acid. [6] Often the terms selenous acid and selenium dioxide are used interchangeably. It reacts with base to form selenite salts containing the SeO 2− 3 anion.

  9. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol is a 2-carbon alcohol. Its molecular formula is CH 3 CH 2 OH. The structure of the molecule of ethanol is CH 3 −CH 2OH (an ethyl group linked to a hydroxyl group), which indicates that the carbon of a methyl group (CH 3 −) is attached to the carbon of a methylene group (−CH 2 –), which is