When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Butane - Wikipedia

    en.wikipedia.org/wiki/Butane

    Butane (/ ˈ b juː t eɪ n /) is an alkane with the formula C 4 H 10. Butane exists as two isomers, n -butane with connectivity CH 3 CH 2 CH 2 CH 3 and iso-butane with the formula (CH 3 ) 3 CH . Both isomers are highly flammable, colorless, easily liquefied gases that quickly vaporize at room temperature and pressure.

  3. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    A completely polar bond is more correctly called an ionic bond, and occurs when the difference between electronegativities is large enough that one atom actually takes an electron from the other. The terms "polar" and "nonpolar" are usually applied to covalent bonds, that is, bonds where the polarity is not complete. To determine the polarity ...

  4. Butane (data page) - Wikipedia

    en.wikipedia.org/wiki/Butane_(data_page)

    The handling of this chemical may incur notable safety precautions. ... Vapor pressure of n-butane. From formula: ... additional terms may apply.

  5. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  6. 1-Butanol - Wikipedia

    en.wikipedia.org/wiki/1-Butanol

    1-Butanol, also known as butan-1-ol or n-butanol, is a primary alcohol with the chemical formula C 4 H 9 OH and a linear structure. Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. The unmodified term butanol usually refers to the straight chain isomer.

  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. 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).

  9. C4H10 - Wikipedia

    en.wikipedia.org/wiki/C4H10

    The molecular formula C 4 H 10 (molar mass: 58.12 g/mol, exact mass: 58.0783 u) may refer to: Butane , or n -butane Isobutane , also known as methylpropane or 2-methylpropane