Among the following compounds (I-III),the cor | vedclass

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(C) The reactivity of benzene derivatives towards electrophilic substitution depends on the electron density of the benzene ring.$I$ (Anisole) has a $

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$I > II > III$

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(C) The reactivity of benzene derivatives towards electrophilic substitution depends on the electron density of the benzene ring.$I$ (Anisole) has a $-OCH_3$ group,which is an electron-donating group $(EDG)$ via resonance ($+M$ effect),significantly increasing the electron density of the benzene ring.$II$ (Benzene) has no substituents.$III$ (Nitrobenzene) has a $-NO_2$ group,which is a strong electron-withdrawing group $(EWG)$ via both inductive $(-I)$ and resonance $(-M)$ effects,significantly decreasing the electron density of the benzene ring.Since electrophiles are electron-deficient species,they react faster with rings having higher electron density.Therefore,the order of reactivity is $I > II > III$.

Among the following compounds $(I-III)$,the correct order of reactivity towards electrophilic substitution is:

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