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Explain bromination of benzene requires...

Explain bromination of benzene requires `FeBr_3` as catalyst, while bromination of anisole `(C_6H_5OCH_3)` does not require any catalyst.

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Since benzene molecule is not so reactive, for bromination it requires more reactive bromine cation `(Boverset(oplus)(r))` or the complex `Br - overset(oplus)(B)r - overset(Θ)(F)eBr_(3)` as the electrophile. Due to the presence of electron-donating `(+R)` methoxy `(-OCH_(3))` group, the anisole ring becomes much more reactive towards electrophillic substitution reaction. When the non-polar bromine molecule comes in contact with the anisole ring, it becomes partially polarised `(overset(delta+)(Br) - overset(delta-)(Br))` and its positive end (weak electrophile) undergoes easy attack by anisole. Therefore, due to greater reactivity of anisole its bromination requires no catalyst.
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Knowledge Check

  • In the oxidation of C_6H_5-CH_2-CH_3 by KMnO_4 the product formed is

    A
    `C_6H_5-CH_2-CHO`
    B
    `C_6H_5-CH_2-COOH`
    C
    `C_6H_5-COOH`
    D
    `C_6H_5-CH_2-OH`
  • The number of C and H - atoms that in the same plane in a toluene (C_(6)H_(5)CH_(3)) molecule is respectively-

    A
    7 and 5
    B
    6 and 5
    C
    7 and 3
    D
    6 and 3
  • A hydrocarbon of molecular formula C_7H_12 on catalytic hydrogenation over platinum gives C_7H_16 the parent hydrocarbon adds bromine and also reacts with [Ag(NH_3)_2]OH to give a precipitate the parent hydrocarbon is

    A
    `CH_3-CH=CH-CH=CH-CH_2-CH_3`
    B
    `CH_3-CH_2-C-=C-CH_2-CH_3`
    C
    `(CH_3)_3C-CH_2-C-=CH`
    D
    `CH_3-CH=CH-CH_2-CH=CH-CH_3`
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