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  2. 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.

  3. Descriptor (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Descriptor_(Chemistry)

    The terms sec and tert are considered obsolete and should only be used for unsubstituted sec-butoxy, sec-butyl [26] [27] or tert-butyl groups. [ 28 ] [ 27 ] There are various spellings such as "sec-butyl", "s-butyl", "sBu" or "bus" which are also considered obsolete.

  4. Butanol - Wikipedia

    en.wikipedia.org/wiki/Butanol

    Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).

  5. tert-Butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_alcohol

    tert-Butyl alcohol is used as a solvent, ethanol denaturant, paint remover ingredient, and gasoline octane booster and oxygenate.It is a chemical intermediate used to produce methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE) by reaction with methanol and ethanol, respectively, and tert-butyl hydroperoxide (TBHP) by reaction with hydrogen peroxide.

  6. 2-Butanol - Wikipedia

    en.wikipedia.org/wiki/2-Butanol

    Butan-2-ol, or sec-butanol, is an organic compound with formula C H 3 CH(OH)CH 2 CH 3. Its structural isomers are 1-butanol , isobutanol , and tert -butanol . 2-Butanol is chiral and thus can be obtained as either of two stereoisomers designated as ( R )-(−)-butan-2-ol and ( S )-(+)-butan-2-ol.

  7. Isobutanol - Wikipedia

    en.wikipedia.org/wiki/Isobutanol

    Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH 3) 2 CHCH 2 OH (sometimes represented as i-BuOH).This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters.

  8. Isobutylamine - Wikipedia

    en.wikipedia.org/wiki/Isobutylamine

    Isobutylamine is an organic chemical compound (specifically, an amine) with the formula (CH 3) 2 CHCH 2 NH 2, and occurs as a colorless liquid. [1] [2] Isobutylamine is one of the four isomeric amines of butane, the others being n-butylamine, sec-butylamine and tert-butylamine.

  9. sec-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/Sec-Butylbenzene

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