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  2. tert-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylbenzene

    tert-Butylbenzene is an organic compound classified as an aromatic hydrocarbon. Its structure consists of a benzene ring substituted with a tert -butyl group . It is a flammable colorless liquid which is nearly insoluble in water but miscible with organic solvents.

  3. 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.

  4. Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/Butylbenzene

    Butylbenzene may refer to: n-Butylbenzene; sec-Butylbenzene; Isobutylbenzene; tert-Butylbenzene; See also. Isobutylbenzene This page was last edited on 28 April 2023 ...

  5. 4-tert-Butylcatechol - Wikipedia

    en.wikipedia.org/wiki/4-tert-Butylcatechol

    4-tert-Butylcatechol (TBC) is an organic chemical compound which is a derivative of catechol. [1] TBC is available in the form of a solid crystal flake [ 2 ] and 85% solution in methanol [ 3 ] or water.

  6. C4-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C4-Benzenes

    The C 4-benzenes are a class of organic aromatic compounds which contain a benzene ring and four other carbon atoms. There are three tetramethylbenzenes, six dimethylethylbenzenes, three diethylbenzenes, three isopropylmethylbenzenes, three n-propylmethylbenzenes and four butylbenzenes.

  7. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.

  8. n-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/N-Butylbenzene

    n-Butylbenzene is the organic compound with the formula C 6 H 5 C 4 H 9. 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.

  9. Category:Tert-butyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Tert-butyl_compounds

    Tert-Butyl chloride; Tert-Butyl hydroperoxide; Tert-Butyl isocyanide; Butyl PBD; Tert-Butylamine; Butylated hydroxyanisole; Butylated hydroxytoluene; 4-tert-Butylbenzaldehyde; N-tert-Butylbenzenesulfinimidoyl chloride; Para-tert-Butylbenzoic acid; 4-tert-Butylcatechol; Tert-Butyldiphenylsilyl; Tert-Butylhydroquinone; Tert-Butyllithium; Tert ...