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  2. 2,4,6-Tribromophenol - Wikipedia

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

    2,4,6-Tribromophenol (TBP) is a brominated derivative of phenol. It is used as a fungicide , as a wood preservative, and an intermediate in the preparation of flame retardants . Production

  3. Bromophenol - Wikipedia

    en.wikipedia.org/wiki/Bromophenol

    Bromophenol. A bromophenol is an organic compound consisting of hydroxyl groups and bromine atoms bonded to a benzene ring. They may be viewed as hydroxyl derivatives of bromobenzene, or as brominated derivatives of phenol. There are five basic types of bromophenols (mono- to pentabromophenol) and 19 different bromophenols in total when ...

  4. Bromine test - Wikipedia

    en.wikipedia.org/wiki/Bromine_test

    The formation of a brominated phenol (i.e. 2,4,6-tribromophenol) or aniline (i.e. 2,4,6-tribromoaniline) in form of a white precipitate indicates that the unknown was a phenol or aniline. The more unsaturated an unknown is, the more bromine it reacts with, and the less coloured the solution will appear.

  5. 2,4,6-Trichlorophenol - Wikipedia

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

    2,4,6-Trichlorophenol, also known as TCP, phenaclor, Dowicide 2S, Dowcide 2S, omal, is a chlorinated phenol that has been used as a fungicide, herbicide, insecticide, antiseptic, [3] defoliant, and glue preservative. [4] It is a clear to yellowish crystalline solid with a strong, phenolic odor. It decomposes on heating to produce toxic and ...

  6. Hydrogen bromide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_bromide

    Hydrogen bromide prepared by the above methods can be contaminated with Br 2, which can be removed by passing the gas through a solution of phenol at room temperature in tetrachloromethane or other suitable solvent (producing 2,4,6-tribromophenol and generating more HBr in the process) or through copper turnings or copper gauze at high ...

  7. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    The regiochemistry of halogenation changes in strongly acidic solutions where PhOH 2] + predominates. Phenol reacts with dilute nitric acid at room temperature to give a mixture of 2-nitrophenol and 4-nitrophenol while with concentrated nitric acid, additional nitro groups are introduced, e.g. to give 2,4,6-trinitrophenol.

  8. Adsorbable organic halides - Wikipedia

    en.wikipedia.org/wiki/Adsorbable_organic_halides

    The reaction in figure 2 shows the reductive debromination of 2,4,6-tribromophenol (2,4,6-TBP) by Ochrabactrum. [13] Based on the relative degradation of the molecule along with analytical results, it has been postulated that degradation of 2,4,6-TBP proceeds through debromination of ortho -bromine in the first step by a dehalogenase to yield 2 ...

  9. Monobromophenol - Wikipedia

    en.wikipedia.org/wiki/Monobromophenol

    The monobromophenols are chemical compounds consisting of phenol substituted with a bromine atom. There are three isomers, 2-bromophenol, 3-bromophenol, and 4-bromophenol. Bromophenols. IUPAC name. 2-Bromophenol. 3-Bromophenol.