On nitration, the major product that chlorobenzene gives is:
A
1-chloro-4-nitrobenzene
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B
1-chloro-3-nitrobenzene
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C
1, 4-dinitrobenzene
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D
2, 4, 6-trinitrobenzene
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Solution
The correct option is A 1-chloro-4-nitrobenzene Since, Cl− group attached to benzene is ortho and para directing, so it forms o− and p− chloronitrobenzene as products in electrophilic substitution reaction of chlorobenzene.
Here the major product is p-chloronitrobenzene because ortho is disfavourd due to inductive effect and steric hindrance. Hence correct option is a.
Intermediates of electrophilic substitution reaction:
In para substituted, E+ and Y=Cl are apart so there is negligible interaction
In ortho substituted, E+ and Y=Cl are close so there is more interaction.
As the size of electrophile increases, percentage of para product increases because E+ and Y=Cl are apart so there is negligible interaction betweem them. The % of ortho and para product formed is depicted below in table with various electrophiles.