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  2. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Because of its extreme reactivity, fluorine (F 2) represents a special category with respect to halogenation. Most organic compounds, saturated or otherwise, burn upon contact with F 2, ultimately yielding carbon tetrafluoride. By contrast, the heavier halogens are far less reactive toward saturated hydrocarbons.

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  4. Propylene - Wikipedia

    en.wikipedia.org/wiki/Propylene

    Propylene, also known as propene, is an unsaturated organic compound with the chemical formula CH 3 CH=CH 2.It has one double bond, and is the second simplest member of the alkene class of hydrocarbons.

  5. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    The relative rates at which different halogens react vary considerably: [citation needed] fluorine (108) > chlorine (1) > bromine (7 × 10 −11) > iodine (2 × 10 −22).. Radical fluorination with the pure element is difficult to control and highly exothermic; care must be taken to prevent an explosion or a runaway reaction.

  6. Cis-trans isomerase - Wikipedia

    en.wikipedia.org/wiki/Cis-trans_isomerase

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  8. Nernst equation - Wikipedia

    en.wikipedia.org/wiki/Nernst_equation

    In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction (half-cell or full cell reaction) from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities (often approximated by concentrations) of the chemical species undergoing ...

  9. 1-Butene - Wikipedia

    en.wikipedia.org/wiki/1-Butene

    1-Butene (IUPAC name: But-1-ene, also known as 1-butylene) is the organic compound with the formula CH 3 CH 2 CH=CH 2.It is a colorless gas. But-1-ene is an alkene easily condensed to give a colorless liquid.