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  2. 2-Methyl-2-butene - Wikipedia

    en.wikipedia.org/wiki/2-Methyl-2-butene

    2-Methyl-2-butene, 2m2b, 2-methylbut-2-ene, beta-isoamylene, or Trimmethylethylene is an alkene hydrocarbon with the molecular formula C 5 H 10. Used as a free radical scavenger in trichloromethane (chloroform) and dichloromethane (methylene chloride). It is also used to scavenge hypochlorous acid (HOCl) in the Pinnick oxidation.

  3. File:2-methyl-2-butene.png - Wikipedia

    en.wikipedia.org/wiki/File:2-methyl-2-butene.png

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  4. Prilezhaev reaction - Wikipedia

    en.wikipedia.org/wiki/Prilezhaev_reaction

    For example, the relative rates of epoxidation increase upon methyl substitution of the alkene (the methyl groups increase the electron density of the double bond by hyperconjugation): ethylene (1, no methyl groups), propene (24, one methyl group), cis-2-butene (500, two methyl groups), 2-methyl-2-butene (6500, three methyl groups), 2,3 ...

  5. File:Structural formula of 2-methyl-2-butene.svg - Wikipedia

    en.wikipedia.org/wiki/File:Structural_formula_of...

    The following other wikis use this file: Usage on ar.wikipedia.org 2-ميثيل-2-بوتين; Usage on de.wikipedia.org Olefine; 2-Methyl-2-buten

  6. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    2-Methyl-2-butene (CAS 513-35-9) Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  7. Lindgren oxidation - Wikipedia

    en.wikipedia.org/wiki/Lindgren_oxidation

    Lindgren oxidation is a selective method for oxidizing aldehydes to carboxylic acids. [1] The reaction is named after Bengt O. Lindgren. The oxidation takes place in water containing solvent mixtures under slightly acidic conditions (pH 3–5) with sodium chlorite as oxidizer.

  8. Paternò–Büchi reaction - Wikipedia

    en.wikipedia.org/wiki/Paternò–Büchi_reaction

    With substrates benzaldehyde and 2-methyl-2-butene the reaction product is a mixture of structural isomers: Another substrate set is benzaldehyde and furan [4] or heteroaromatic ketones and fluorinated alkenes. [5] The alternative strategy for the above reaction is called the Transposed Paternò−Büchi reaction.

  9. tert-Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Amyl_alcohol

    tert-Amyl alcohol (TAA) or 2-methylbutan-2-ol (2M2B), is a branched pentanol. Historically, TAA has been used as an anesthetic [ 3 ] and more recently as a recreational drug . [ 4 ] TAA is mostly a positive allosteric modulator for GABA A receptors in the same way as ethanol . [ 5 ]