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  2. Chlorine - Wikipedia

    en.wikipedia.org/wiki/Chlorine

    Corresponding to periodic trends, it is intermediate in electronegativity between fluorine and bromine (F: 3.98, Cl: 3.16, Br: 2.96, I: 2.66), and is less reactive than fluorine and more reactive than bromine. It is also a weaker oxidising agent than fluorine, but a stronger one than bromine.

  3. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Bond energies to bromine tend to be lower than those to chlorine but higher than those to iodine, and bromine is a weaker oxidising agent than chlorine but a stronger one than iodine. This can be seen from the standard electrode potentials of the X 2 /X − couples (F, +2.866 V; Cl, +1.395 V; Br, +1.087 V; I, +0.615 V; At, approximately +0.3 V).

  4. Food chain - Wikipedia

    en.wikipedia.org/wiki/Food_chain

    Food chain in a Swedish lake. Osprey feed on northern pike, which in turn feed on perch which eat bleak which eat crustaceans.. A food chain is a linear network of links in a food web, often starting with an autotroph (such as grass or algae), also called a producer, and typically ending at an apex predator (such as grizzly bears or killer whales), detritivore (such as earthworms and woodlice ...

  5. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Bond energies to bromine tend to be lower than those to chlorine but higher than those to iodine, and bromine is a weaker oxidising agent than chlorine but a stronger one than iodine. This can be seen from the standard electrode potentials of the X 2 /X − couples (F, +2.866 V; Cl, +1.395 V; Br, +1.087 V; I, +0.615 V; At, approximately +0.3 V).

  6. Chemoselectivity - Wikipedia

    en.wikipedia.org/wiki/Chemoselectivity

    The carbon-bromine bond is more reactive than the carbon-fluorine bond. If a molecule has several potential reactive sites, the reaction will occur in the most reactive one. When comparing carbon-halogen bonds, lighter halogens such as fluorine and chlorine have a better orbital overlap with carbon, which makes the bond stronger. [4]

  7. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    Chain termination Two free radicals (chlorine and chlorine, chlorine and methyl, or methyl and methyl) combine: Methane chlorination: termination The last possibility generates in an impurity in the final mixture (notably, an organic molecule with a longer carbon chain than the reactants). The net reaction is: Methane chlorination overall reaction

  8. Biological roles of the elements - Wikipedia

    en.wikipedia.org/wiki/Biological_roles_of_the...

    bromine: 35: 5: Essential to membrane architecture and tissue development in animals. [23] May have antibiotic effects in some compounds when it substitutes for chlorine. [24] Bromine compounds are very common in and presumably essential to a variety of marine organisms, including bacteria, fungi, seaweeds, and diatoms.

  9. Reactivity–selectivity principle - Wikipedia

    en.wikipedia.org/wiki/Reactivity–selectivity...

    The sulfur radical was found to be more reactive (6*10 8 vs. 1*10 7 M −1.s −1) and less selective (selectivity ratio 76 vs 1200) than the carbon radical. In this case, the effect can be explained by extending the Bell–Evans–Polanyi principle with a factor δ {\displaystyle \delta \,} accounting for transfer of charge from the reactants ...