$A$ compound $X$ formed after heating coke with lime reacts with water to give $Y$,which on passing over red-hot iron at $873 \ K$ produces $Z$. The compound $Z$ is

  • A
    Benzene
  • B
    Hexane
  • C
    Cyclohexane
  • D
    Hexene

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The following compound has four aromatic rings marked as $A$,$B$,$C$ and $D$. Rank them in terms of increasing reactivity towards electrophilic aromatic substitution?

Out of benzene,$m$-dinitrobenzene and toluene,which will undergo nitration most easily and why?

Identify the number of aromatic compounds from the following structures:
$(I)$ Cyclopentadiene
$(II)$ Cyclooctatetraene
$(III)$ Borazine $(B_3N_3H_6)$
$(IV)$ $1,4-$diboracyclohexa$-2,5-$diene

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The cyclopentadienyl anion is:

The electrophile,$E^{+}$,attacks the benzene ring to generate the intermediate $\sigma$-complex. Which $\sigma$-complex is of lowest energy?

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