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  2. n-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/N-Butylbenzene

    Of two isomers of butylbenzene, n-butylbenzene consists of a phenyl group attached to the 1 position of a butyl group. It is a slightly greasy, colorless liquid. The synthesis of n-butylbenzene by the reaction of chlorobenzene and butylmagnesium bromide was one of the first demonstrations of the Kumada coupling using nickel diphosphine ...

  3. C4-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C4-Benzenes

    There are three tetramethylbenzenes, six dimethylethylbenzenes, three diethylbenzenes, three isopropylmethylbenzenes, three n-propylmethylbenzenes and four butylbenzenes. The saturated compounds have formula C 10 H 14 and molecular weight 134.22 g/mol. C 4-benzenes are found in petroleum. [1] Petrol (gasoline) can contain 5-8% C 4-benzenes. [2]

  4. C10H14 - Wikipedia

    en.wikipedia.org/wiki/C10H14

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  5. Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/Butylbenzene

    Personal tools. Donate; Create account; Log in; Pages for logged out editors learn more. ... Butylbenzene may refer to: n-Butylbenzene; sec-Butylbenzene; Isobutylbenzene;

  6. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The word "butyl" is derived from butyric acid, a four-carbon carboxylic acid found in rancid butter. [1] The name "butyric acid" comes from Latin butyrum , butter . Subsequent preferred IUPAC names for alkyl radicals in the series are simply named from the Greek number that indicates the number of carbon atoms in the group: pentyl , hexyl ...

  7. Category:C4-Benzenes - Wikipedia

    en.wikipedia.org/wiki/Category:C4-Benzenes

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  8. C3-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C3-Benzenes

    The C 3-benzenes are a class of organic aromatic compounds which contain a benzene ring and three other carbon atoms. For the hydrocarbons with no further unsaturation, there are four isomers.

  9. N-tert-Butylbenzenesulfinimidoyl chloride - Wikipedia

    en.wikipedia.org/wiki/N-Tert-butylbenzenesulfini...

    N-tert-Butylbenzenesulfinimidoyl chloride is a useful oxidant for organic synthesis reactions. [1] It is a good electrophile, and the sulfimide S=N bond can be attacked by nucleophiles, such as alkoxides, enolates, and amide ions. The nitrogen atom in the resulting intermediate is basic, and can abstract an α-hydrogen to create a new double bond.