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  2. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    For example, consider radical bromination of toluene: [5] bromination of toluene with hydrobromic acid and hydrogen peroxide in water. This reaction takes place on water instead of an organic solvent and the bromine is obtained from oxidation of hydrobromic acid with hydrogen peroxide. An incandescent light bulb suffices to radicalize.

  3. Light-dependent reactions - Wikipedia

    en.wikipedia.org/wiki/Light-dependent_reactions

    In oxygenic photosynthesis, the first electron donor is water, creating oxygen (O 2) as a by-product. In anoxygenic photosynthesis, various electron donors are used. Cytochrome b 6 f and ATP synthase work together to produce ATP (photophosphorylation) in two distinct ways.

  4. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    Nitration of toluene gives mono-, di-, and trinitrotoluene, all of which are widely used. Dinitrotoluene is the precursor to toluene diisocyanate, a precursor to polyurethane foam. Trinitrotoluene (TNT) is an explosive. Complete hydrogenation of toluene gives methylcyclohexane. The reaction requires a high pressure of hydrogen and a catalyst.

  5. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Following the usual trend, bromine is less reactive and iodine least of all. Of the many reactions possible, illustrative is the formation of gold(III) chloride by the chlorination of gold . The chlorination of metals is usually not very important industrially since the chlorides are more easily made from the oxides and hydrogen chloride .

  6. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    The reaction mechanism for an alkene bromination can be described as follows. In the first step of the reaction, a bromine molecule approaches the electron-rich alkene carbon–carbon double bond. The bromine atom closer to the bond takes on a partial positive charge as its electrons are repelled by the electrons of the double bond.

  7. Calvin cycle - Wikipedia

    en.wikipedia.org/wiki/Calvin_cycle

    Calvin cycle step 1 (black circles represent carbon atoms) Calvin cycle steps 2 and 3 combined. The enzyme RuBisCO catalyses the carboxylation of ribulose-1,5-bisphosphate, RuBP, a 5-carbon compound, by carbon dioxide (a total of 6 carbons) in a two-step reaction. [6] The product of the first step is enediol-enzyme complex that can capture CO 2 ...

  8. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    The initial step of the halogenation of aromatic compounds differs from that of the halogenation of alkenes in that alkenes do not require a catalyst to enhance the electrophilicity of the halogen. The formation of the arenium ion results in the temporary loss of aromaticity , which has a higher activation energy compared to halonium ion ...

  9. Photorespiration - Wikipedia

    en.wikipedia.org/wiki/Photorespiration

    C 2 photosynthesis (also called glycine shuttle and photorespiratory CO 2 pump) is a CCM that works by making use of – as opposed to avoiding – photorespiration. It performs carbon refixation by delaying the breakdown of photorespired glycine, so that the molecule is shuttled from the mesophyll into the bundle sheath .