The number of disubstituted products of benzene is

  • A
    $2$
  • B
    $3$
  • C
    $4$
  • D
    $5$

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Similar Questions

Match the following reactions given in Column-$I$ with their respective names in Column-$II$:
Column-$I$ Column-$II$
$(i)$ $\text{Benzene} + \text{Conc. } HNO_3 + \text{Conc. } H_2SO_4 \rightarrow \text{Nitrobenzene}$ $(A)$ $\text{Halogenation}$
$(ii)$ $\text{Benzene} + Cl_2 \xrightarrow{\text{Anhy. } AlCl_3} \text{Chlorobenzene}$ $(B)$ $\text{Nitration}$
$(iii)$ $\text{Benzene} + CH_3Cl \xrightarrow{\text{Anhy. } AlCl_3} \text{Toluene}$ $(C)$ $\text{Friedel-Crafts acylation}$
$(iv)$ $\text{Benzene} + CH_3COCl \xrightarrow{\text{Anhy. } AlCl_3} \text{Acetophenone}$ $(D)$ $\text{Friedel-Crafts alkylation}$

Given below are two statements $:$
Statement $(I) :$ On nitration of $m-$xylene with $HNO_3, H_2SO_4$ followed by oxidation,$4-$nitrobenzene$-1, 3-$dicarboxylic acid is obtained as the major product.
Statement $(II) :$ $-CH_3$ group is $o/p-$directing while $-NO_2$ group is $m-$directing group.
In the light of the above statements,choose the correct answer from the options given below $:$

How would you convert the following compounds into benzene?
$(i)$ Ethyne
$(ii)$ Ethene
$(iii)$ Hexane

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Which among the following pairs of the structures will give different products on ozonolysis? (Consider the double bonds in the structures are rigid and not delocalized.)

Which of the following undergoes sulphonation at the fastest rate?

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