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  2. Isobutylene - Wikipedia

    en.wikipedia.org/wiki/Isobutylene

    Isobutylene (or 2-methylpropene) is a hydrocarbon with the chemical formula (CH 3) 2 C=CH 2. It is a four-carbon branched alkene (olefin), one of the four isomers of butylene . It is a colorless flammable gas, and is of considerable industrial value.

  3. 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 .

  4. 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.

  5. 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 ...

  6. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    For example, of the isomers of butene, the two methyl groups of (Z)-but-2-ene (a.k.a. cis-2-butene) appear on the same side of the double bond, and in (E)-but-2-ene (a.k.a. trans-2-butene) the methyl groups appear on opposite sides. These two isomers of butene have distinct properties.

  7. Benson group increment theory - Wikipedia

    en.wikipedia.org/wiki/Benson_group_increment_theory

    This is a thermodynamic argument, and kinetics are ignored. As determined by the enthalpies below the corresponding molecules, the enthalpy of reaction for 2-methyl-1-butene going to 2-methyl-butane is −29.07 kcal/mol, which is in great agreement with the value calculated from NIST, [15] −28.31 kcal/mol. For 2-butanone going to 2-butanol ...

  8. List of UN numbers 2401 to 2500 - Wikipedia

    en.wikipedia.org/wiki/List_of_UN_numbers_2401_to...

    6.1: Nitrocresols: UN 2447: 4.2: Phosphorus white, molten UN 2448: 4.1: Sulfur, molten UN 2449? (UN No. no longer in use) Oxalates (UN No. no longer in use) [2] UN 2450? (UN No. no longer in use) UN 2451: 2: Nitrogen trifluoride, compressed UN 2452: 2: Ethylacetylene, inhibited UN 2453: 2: Ethyl fluoride or Refrigerant gas R 161 UN 2454: 2 ...

  9. Dinoseb - Wikipedia

    en.wikipedia.org/wiki/Dinoseb

    The first step in the synthesis of dinoseb is the synthesis of 2-(1-methylpropyl)phenol from 1-butene and phenol. [20] First, 1-butene is protonated so that a secondary carbocation is formed. This can only happen under acidic conditions. The formed carbocation can undergo electrophilic aromatic substitution with phenol. The product of this ...