The structure of the product will be:

  • A
    p-Nitroaniline
  • B
    p-Aminoazobenzene
  • C
    p-Hydroxyazobenzene
  • D
    $4$,$4$'-Dihydroxyazobenzene

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Similar Questions

Identify $C$ in the following reaction sequence:
$Cyclohexanone$ $\xrightarrow[\text{Alkaline medium}]{HCN} A$ $\xrightarrow{LiAlH_4} B$ $\xrightarrow{NaNO_2/HCl} C$

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The end product $(C)$ is

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Match List-$I$ with List-$II$.
List-$I$ (Mixture of Compounds) List-$II$ (Reagent used to distinguish)
$A$. Diethyl amine + Ethyl amine $I$. Bromine water
$B$. Acetaldehyde + Acetone $II$. $CHCl_3 + KOH, \Delta$
$C$. Ethanol + Phenol $III$. Neutral $FeCl_3$
$D$. Benzoic acid + Cinnamic acid $IV$. Ammonical silver nitrate

The product $(A)$ of the given reaction is:

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Give a plausible explanation for each of the following:
$(i)$ Why are amines less acidic than alcohols of comparable molecular masses?
$(ii)$ Why do primary amines have higher boiling points than tertiary amines?
$(iii)$ Why are aliphatic amines stronger bases than aromatic amines?

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