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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. tert-Butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_alcohol

    tert-Butyl alcohol is the simplest tertiary alcohol, with a formula of (CH 3) 3 COH (sometimes represented as t -BuOH). Its isomers are 1-butanol, isobutanol, and butan-2-ol. tert -Butyl alcohol is a colorless solid, which melts near room temperature and has a camphor -like odor. It is miscible with water, ethanol and diethyl ether.

  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. 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.

  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 (O H)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. It is normally encountered as a 1:1 mixture of the ...

  7. tert-Butyl isocyanide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_isocyanide

    Infobox references. tert-Butyl isocyanide is an organic compound with the formula Me 3 CNC (Me = methyl, CH 3). It is an isocyanide, commonly called isonitrile or carbylamine, as defined by the functional group C≡N-R. tert -Butyl isocyanide, like most alkyl isocyanides, is a reactive colorless liquid with an extremely unpleasant odor.

  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. It is the decarboxylated form of the amino acid valine, and the ...

  9. Butyl butyrate - Wikipedia

    en.wikipedia.org/wiki/Butyl_butyrate

    Butyl butyrate, or butyl butanoate, is an organic compound that is an ester formed by the condensation of butyric acid and n -butanol. It is a clear, colorless liquid that is insoluble in water, but miscible with ethanol and diethyl ether. Its refractive index is 1.406 at 20 °C.