explain the electrophilic aromatic substitution reactions with example
Asked by | 8th May, 2008, 03:27: PM
In the first step of the reaction mechanism for this reaction, the electron-rich aromatic ring which in the simplest case is benzene is attacked by the electrophile A. This leads to the formation of a positively-charged cyclohexadienyl cation, also known as an arenium ion. This carbocation is unstable, owing both to the positive charge on the molecule and to the temporary loss of aromaticity. However, the cyclohexadienyl cation is partially stabilized by resonance, which allows the positive charge to be distributed over three carbon atoms.
In the second stage of the reaction, a Lewis base B donates electrons to the hydrogen atom at the point of electrophilic attack, and the electrons shared by the hydrogen return to the pi system, restoring aromaticity.
An electrophilic substitution reaction on benzene does not always result in monosubstitution. While electrophilic substituents usually withdraw electrons from the aromatic ring and thus deactivate it against further reaction, a sufficiently strong electrophile can perform a second or even a third substitution. This is especially the case with the use of catalysts
Answered by | 9th May, 2008, 09:42: AM
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