What is meant by deactivating groups? Explain with suitable examples.

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(N/A) Definition: Groups that,when attached to a benzene ring,make the subsequent electrophilic aromatic substitution reaction slower than that of benzene are known as deactivating groups.
Examples: Most meta-directing groups are deactivating groups,such as $-COOH$,$-NO_2$,$-SO_3H$,$-COCl$,$-COR$,$-COOR$,and $-CN$.
Explanation:
$(a)$ Resonance effect: In meta-directing groups,the $\pi$-electron density of the benzene ring is delocalized towards the substituent group due to resonance. This reduces the electron density within the ring,making it less susceptible to electrophilic attack.
$(b)$ Inductive effect: Most of these groups exert a strong electron-withdrawing inductive effect ($-I$ effect),which pulls electron density away from the ring,further decreasing the electron density and thus deactivating the ring towards electrophilic substitution.

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The reaction$(s)$ leading to the formation of $1,3,5-$trimethylbenzene is (are):
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Which of the following undergoes sulphonation at the fastest rate?

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The increasing order of the reactivity of the following compounds towards electrophilic aromatic substitution reaction is:

Given below are two statements,one is labelled as Assertion $A$ and the other is labelled as Reason $R$.
Assertion $A$ : Benzene is more stable than hypothetical cyclohexatriene.
Reason $R$ : The delocalized $\pi$ electron cloud is attracted more strongly by nuclei of carbon atoms.
In the light of the above statements,choose the correct answer from the options given below:

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