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i think the question is wrong.benzene doesn't respond nucleophilic substitution respond electrophilic substitution it is electrophilic then due to resonance there is a partial double bond between carbon of benzene and halogens.so halobenzenes are chemically inert towards electrophilic substitution.
electrophilic substitution. and UV light or heat is required to all the reaction to proceed
aniline would go through an electrophilic substitution, it is a weak base
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electrophilic attack
R. C. Poller has written: 'Electrophilic aromatic substitution'
When a positive ion (electrophile) attacks on a pi bond or partially negative carbon atom and replace H as a positive ion then it is electrophilic substitution reaction.
the electron in benzene are delocalised making d ring to be elctron rich,thereby undergoing electrophilic substitution.benzene cannot undergo nucleophillic substitution,it can only undergo if it is substituted with an electron withdrawing group
As there is an availability of lone pair of electrons on chlorine, it directs the benzene ring towards electrophilic substitution at ortho and para positions.. When we will draw the resonating structures of chloro benzene,we will see that negative charge resides at orho and para positions..
alkenes are neutral nucleofiles they undergoes electrophilic addition reactions.
2-nitro toluene may under go electrophilic substitution reactions as Nitration, Halogenation at 4th position.
A nucleophile attacks an electrophilic site and replaces a leaving group. e.g. OH- attacks R-Br to give R-OH.