Benzene shows

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Question

(D) Benzene is a stable aromatic compound due to the delocalization of $\pi$-electrons. Because of this stability,it primarily undergoes electrophilic

Vedclass · Accepted Answer

All of these

Vedclass · Answer

(D) Benzene is a stable aromatic compound due to the delocalization of $\pi$-electrons. Because of this stability,it primarily undergoes electrophilic substitution reactions rather than addition reactions,as addition would destroy the aromaticity. However,under specific conditions,benzene can undergo addition reactions (e.g.,hydrogenation to cyclohexane). Furthermore,alkyl-substituted benzenes can undergo oxidation of the side chain using strong oxidizing agents like alkaline $KMnO_4$. Since benzene and its derivatives exhibit all these types of reactions under appropriate conditions,the correct answer is $All \ of \ these$.

Similar Questions

What is aromaticity? Explain with suitable examples. State the Huckel rule and explain it with a suitable example. Write the requirements for aromatic character in a compound. Show aromatic structures having $1$,$2$,and $3$ rings with suitable examples.

Find the decreasing order of reactivity towards electrophilic substitution reaction for the following compounds:
$I$: Toluene $(C_6H_5CH_3)$
$II$: Benzene $(C_6H_6)$
$III$: Anisole $(C_6H_5OCH_3)$
$IV$: Trifluoromethylbenzene $(C_6H_5CF_3)$

Among the following,reaction$(s)$ which give$(s)$ tert-butylbenzene as the major product is(are):

Product $(A)$ is

What are $X$ and $Y$ in the following reactions?

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