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  2. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Bromine addition to alkene reaction mechanism. An old qualitative test for the presence of the alkene functional group is that alkenes turn brown aqueous bromine solutions colourless, forming a bromohydrin with some of the dibromoalkane also produced. The reaction passes through a short-lived strongly electrophilic bromonium intermediate.

  3. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Industrially, it is mainly produced by the reaction of hydrogen gas with bromine gas at 200–400 °C with a platinum catalyst. However, reduction of bromine with red phosphorus is a more practical way to produce hydrogen bromide in the laboratory: [2] 2 P + 6 H 2 O + 3 Br 2 → 6 HBr + 2 H 3 PO 3 H 3 PO 3 + H 2 O + Br 2 → 2 HBr + H 3 PO 4

  4. Bromine water - Wikipedia

    en.wikipedia.org/wiki/Bromine_water

    Bromine water, Br 2. Bromine water is an oxidizing, intense brown mixture containing diatomic bromine (Br 2) dissolved in water (H 2 O). [1] It is often used as a reactive in chemical assays of recognition for substances which react with bromine in an aqueous environment with the halogenation mechanism, mainly unsaturated carbon compounds (carbon compounds with 1 or more double or triple bond(s)).

  5. Properties of nonmetals (and metalloids) by group - Wikipedia

    en.wikipedia.org/wiki/Properties_of_nonmetals...

    Metal chlorides are largely ionic in nature. The common oxide of chlorine (Cl 2 O 7) is strongly acidic. Liquid bromine. Bromine is a deep brown diatomic liquid that is quite reactive, and has a liquid density of 3.1028 g/cm 3. It boils at 58.8 °C and solidifies at −7.3 °C to an orange crystalline solid (density 4.05 g/cm −3). It is the ...

  6. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    The reaction details following the usual patterns of electrophilic aromatic substitution: RC 6 H 5 + Br 2 → RC 6 H 4 Br + HBr. A prominent application of this reaction is the production of tetrabromobisphenol-A from bisphenol-A. Free-radical substitution with bromine is commonly used to prepare organobromine compounds.

  7. Reactivity (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Reactivity_(chemistry)

    In pure compounds, reactivity is regulated by the physical properties of the sample. For instance, grinding a sample to a higher specific surface area increases its reactivity. In impure compounds, the reactivity is also affected by the inclusion of contaminants. In crystalline compounds, the crystalline form can also affect reactivity. However ...

  8. 'Dismembered' body of Delaware woman reported missing found ...

    www.aol.com/dismembered-body-delaware-woman...

    A Delaware woman who was reported missing last week after she didn't show up to work for several days was found dismembered in a car over the weekend, police said.

  9. Wohl–Ziegler bromination - Wikipedia

    en.wikipedia.org/wiki/Wohl–Ziegler_bromination

    Rate laws have been developed that describe the competitive behavior of this reaction, and they show a strong dependence on the concentration of molecular bromine; given below are the two equations: one for high concentrations of bromine and one for low concentrations of bromine. [13]