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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. Reactivity–selectivity principle - Wikipedia

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

    A classic example of perceived RSP found in older organic chemistry textbooks concerns the free radical halogenation of simple alkanes. Whereas the relatively unreactive bromine reacts with 2-methylbutane predominantly to 2-bromo-2-methylbutane, the reaction with much more reactive chlorine results in a mixture of all four regioisomers.

  4. Chlorine cycle - Wikipedia

    en.wikipedia.org/wiki/Chlorine_cycle

    Chlorine's ability to completely dissociate in water is also why it is an essential electrolyte in many biological processes. [6] Chlorine, along with phosphorus, is the sixth most common element in organic matter. [1] Cells utilize chloride to balance pH and maintain turgor pressure at equilibrium.

  5. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Bromine is intermediate in reactivity between chlorine and iodine, and is one of the most reactive elements. 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.

  6. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Bromine is a weaker halogenating agent than both fluorine and chlorine, while iodine is the least reactive of them all. The facility of dehydrohalogenation follows the reverse trend: iodine is most easily removed from organic compounds, and organofluorine compounds are highly stable.

  7. 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]

  8. Biological roles of the elements - Wikipedia

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

    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. [25] [26] Most marine organobromine compounds are made by the action of a unique algal enzyme, vanadium ...

  9. 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).