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  2. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    Bromotoluenes are aryl bromides based on toluene in which at least one aromatic hydrogen atom is replaced with a bromine atom. They have the general formula C 7 H 8– n Br n , where n = 1–5 is the number of bromine atoms.

  3. Dehalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehalogenation

    The reaction begins with the formation of alkyl/arene-magnesium-halogen compound, followed by addition of proton source to form dehalogenated product. Egorov and his co-workers have reported dehalogenation of benzyl halides using atomic magnesium in 3P state at 600 °C. Toluene and bi-benzyls were produced as the product of the reaction. [9]

  4. Dow process - Wikipedia

    en.wikipedia.org/wiki/Dow_process

    Dow process (bromine), a method of bromine extraction from brine Dow process (magnesium) , a method of magnesium extraction from brine Dow process (phenol) , a method of phenol production through the hydrolysis of chlorobenzene

  5. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  6. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    Therefore, they are generated by adding iron filings to bromine or chlorine. Here is the mechanism of this reaction: The mechanism for bromination of benzene. The mechanism for iodination is slightly different: iodine (I 2) is treated with an oxidizing agent such as nitric acid to obtain the electrophilic iodine ("I +", probably IONO 2).

  7. 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.

  8. 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 ...

  9. Dow process (bromine) - Wikipedia

    en.wikipedia.org/wiki/Dow_process_(bromine)

    In the original invention, bromide-containing brines are treated with sulfuric acid and bleaching powder to oxidize bromide to bromine, which remains dissolved in the water. The aqueous solution is dripped onto burlap, and air is blown through causing bromine to volatilize. Bromine is trapped with iron turnings to give a solution of ferric bromide.