Shristy Maurya Asked a Question
July 26, 2020 9:19 pmpts 30 pts
Arrange the following compounds in order of decreasing ease of nucleophilic substitution reactions: [BHU 2014] (14-Nitrochlorobenzene (II) 2, 4,6-Trinitrochlorobenzene (a) IV> III> II >I (c) llI > I>I> IV (1I) 2,4-Dinitrochlorobenzene (Iv) Benzyl chloride (b) I> II> II > IV (d) Ill > IV> II>I
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  • Dinesh khalmaniya Best Answer
    C option C
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    Dinesh khalmaniya
    more the -R groups at ortho and para position more is the rate of Nucleophilic substitution
  • Suman Kumar thankyou
    option C is correct.
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  • Suman Kumar
    Since Benzene generally undergo eletrophilic substitution as benzene is eletron rich.
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    Suman Kumar
    So in order to go for nucleophilic reaction in Benzene more the number of eletron withdrawing group more easy will be the reaction