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  2. Photochlorination - Wikipedia

    en.wikipedia.org/wiki/Photochlorination

    Reaction scheme of the photobromination of the methyl group of toluene. Photobromination with elemental bromine proceeds analogous to photochlorination also via a radical mechanism. In the presence of oxygen, the hydrogen bromide formed is partly oxidised back to bromine, resulting in an increased yield. Because of the easier dosage of the ...

  3. Aluminium sulfate - Wikipedia

    en.wikipedia.org/wiki/Aluminium_sulfate

    Aluminium sulfate is a salt with the formula Al 2 (SO 4) 3. It is soluble in water and is mainly used as a coagulating agent (promoting particle collision by neutralizing charge) in the purification of drinking water [ 3 ] [ 4 ] and wastewater treatment plants , and also in paper manufacturing.

  4. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    A few types of aromatic compounds, such as phenol, will react without a catalyst, but for typical benzene derivatives with less reactive substrates, a Lewis acid is required as a catalyst. Typical Lewis acid catalysts include AlCl 3, FeCl 3, FeBr 3 and ZnCl 2. These work by forming a highly electrophilic complex which is attacked by the benzene ...

  5. 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.

  6. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    Toluene (/ ˈ t ɒ l. j u iː n /), also known as toluol (/ ˈ t ɒ l. j u. ɒ l , - ɔː l , - oʊ l / ), is a substituted aromatic hydrocarbon [ 15 ] with the chemical formula C 6 H 5 CH 3 , often abbreviated as PhCH 3 , where Ph stands for the phenyl group.

  7. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  8. Aluminium chloride - Wikipedia

    en.wikipedia.org/wiki/Aluminium_chloride

    Heating this solid does not produce anhydrous aluminium trichloride, the hexahydrate decomposes to aluminium hydroxide when heated: [Al(H 2 O) 6 ]Cl 3 → Al(OH) 3 + 3 HCl + 3 H 2 O Aluminium also forms a lower chloride , aluminium(I) chloride (AlCl), but this is very unstable and only known in the vapour phase.

  9. 4-Toluenesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/4-Toluenesulfonyl_chloride

    4-Toluenesulfonyl chloride (p-toluenesulfonyl chloride, toluene-p-sulfonyl chloride) is an organic compound with the formula CH 3 C 6 H 4 SO 2 Cl. This white, malodorous solid is a reagent widely used in organic synthesis. [2] Abbreviated TsCl or TosCl, it is a derivative of toluene and contains a sulfonyl chloride (−SO 2 Cl) functional group.