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  2. 2,4,6-Tribromoaniline - Wikipedia

    en.wikipedia.org/wiki/2,4,6-tribromoaniline

    2,4,6-Tribromoaniline can be prepared by treating bromine water with aniline in a solution of acetic acid or dilute hydrochloric acid: [1] By reacting bromine with aniline in water, a white precipitate immediately forms and that is 2,4,6-tribromoaniline

  3. 1,3,5-Tribromobenzene - Wikipedia

    en.wikipedia.org/wiki/1,3,5-Tribromobenzene

    Brominating aniline with elemental bromine gives 2,4,6-tribromoaniline. This is then diazotized, then reacted with ethanol to replace the diazonium group with hydrogen, forming 1,3,5-tribromobenzene. [3] It has also been prepared by these methods: [3] replacement of the amino group of 3,5-dibromoaniline with bromine

  4. 4-Bromoaniline - Wikipedia

    en.wikipedia.org/wiki/4-bromoaniline

    4-Bromoaniline is a compound where an aniline molecule is substituted with a bromine atom on the para position. Commercially available, this compound may be used as a building block, e.g. in the preparation of monobrominated biphenyl via the Gomberg-Bachmann reaction .

  5. Aniline - Wikipedia

    en.wikipedia.org/wiki/Aniline

    For example, reaction of aniline with sulfuric acid at 180 °C produces sulfanilic acid, H 2 NC 6 H 4 SO 3 H. If bromine water is added to aniline, the bromine water is decolourised and a white precipitate of 2,4,6-tribromoaniline is formed. To generate the mono-substituted product, a protection with acetyl chloride is required:

  6. Phosphorus tribromide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_tribromide

    PBr 3 is prepared by treating red phosphorus with bromine. An excess of phosphorus is used in order to prevent formation of PBr 5: [1] [2] P 4 + 6 Br 2 → 4 PBr 3. Because the reaction is highly exothermic, it is often conducted in the presence of a diluent such as PBr 3. Phosphorus tribromide is also generated in situ from red phosphorus and ...

  7. Nitrogen tribromide - Wikipedia

    en.wikipedia.org/wiki/Nitrogen_tribromide

    NBr 3 can be produced by the reaction of bromine or hypobromite and ammonia in a dilute aqueous buffer solution. [3] It can also be prepared by the reaction of bromine and bromine azide. [4] Ammonia and bromine undergo glow discharge, and after treatment, red NBr 3 ·6NH 3 can be obtained. [5] Pure nitrogen NBr 3 was only produced in 1975. [6]

  8. 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

  9. 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)).