enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. tert-Butanesulfinamide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butanesulfinamide

    tert-Butanesulfinamide (also known as 2-methyl-2-propanesulfinamide or Ellman's sulfinamide) is an organosulfur compound and a member of the class of sulfinamides. Both enantiomeric forms are commercially available and are used in asymmetric synthesis as chiral auxiliaries, often as chiral ammonia equivalents for the synthesis of amines.

  3. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.

  4. Di-tert-butyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_peroxide

    For this reason di-tert-butyl peroxide is commonly used as a radical initiator in organic synthesis and polymer chemistry. The decomposition reaction proceeds via the generation of methyl radicals. (CH 3) 3 COOC(CH 3) 3 → 2 (CH 3) 3 CO • (CH 3) 3 CO • → (CH 3) 2 CO + CH • 3 2 CH • 3 → C 2 H 6

  5. Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Butyl_bromide

    2-Bromo-2-methylpropane (tert-butyl bromide) This page was last edited on 5 February 2022, at 12:14 (UTC). Text is available under the Creative Commons Attribution ...

  6. Di-tert-butyl ether - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_ether

    This article about an organic compound is a stub. You can help Wikipedia by expanding it.

  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. C4H9Br - Wikipedia

    en.wikipedia.org/wiki/C4H9Br

    5 languages. العربية ... tert-Butyl bromide; 1-bromo-2-methylpropane This page was last edited on 16 August 2021, at 07:47 (UTC). Text is available under the ...

  9. Methyl tert-butyl ether - Wikipedia

    en.wikipedia.org/wiki/Methyl_tert-butyl_ether

    Methyl tert-butyl ether (MTBE), also known as tert-butyl methyl ether, is an organic compound with a structural formula (CH 3) 3 COCH 3. MTBE is a volatile, flammable, and colorless liquid that is sparingly soluble in water. [ 1 ]