enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    In chemistry, halogenation is a chemical reaction which introduces one or more halogens into a chemical compound. Halide-containing compounds are pervasive, making this type of transformation important, e.g. in the production of polymers, drugs. [1] This kind of conversion is in fact so common that a comprehensive overview is challenging.

  4. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  5. On-water reaction - Wikipedia

    en.wikipedia.org/wiki/On-water_reaction

    In one typical example of this reaction at room temperature the chemical yield was found to be 100% on water after 120 h compared with 16% for the same reaction in toluene and 73% in the neat reaction. Enhanced reactivity is also found in cycloadditions.

  6. File:Toluene Halogenation Reactions V.2.svg - Wikipedia

    en.wikipedia.org/wiki/File:Toluene_Halogenation...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  7. Transhalogenation - Wikipedia

    en.wikipedia.org/wiki/Transhalogenation

    An example is the conversion of alkyl chloride into alkyl fluoride: C 3 H 5-Cl + NaF → R-F + NaCl. This kind of reaction is called Finkelstein reaction. [2] However, it is also possible, for example, to produce phosphorus fluoride compounds by transhalogenating chlorine, bromine or iodine bound to phosphorus with a metal fluoride. [3]

  8. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    Regiochemistry follows from the reaction mechanism, which exhibits halogen attack on the least-hindered unsaturated carbon. The mechanism for this chain reaction resembles free radical halogenation, in which the peroxide promotes formation of the bromine radical. However, this process is restricted to addition of HBr.

  9. Category:Halogenation reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Halogenation...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more