Which of the following species would not be involved in the Hoffmann rearrangement shown below?

  • A
    $N$-bromocyclohexanecarboxamide
  • B
    Cyclohexyl isocyanate
  • C
    Nitrene intermediate
  • D
    All of the above are involved in the reaction.

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Three isomers $A$,$B$,and $C$ (molecular formula $C_8H_{11}N$) give the following results:
$A$ and $C$ $\xrightarrow{\text{Diazotization}}$ $P + Q$ $\xrightarrow[(ii) \text{ oxidation } (KMnO_4 + H^{+})]{(i) \text{ Hydrolysis}}$ $R$ (product of $A$) and $S$ (product of $C$)
Identify $A$,$B$,and $C$ from the given options.

Match the reactions given in Column-$I$ with the statements given in Column-$II$.
Column-$I$ Column-$II$
$A$. Ammonolysis $1$. Amine with lesser number of carbon atoms
$B$. Gabriel phthalimide synthesis $2$. Detection test for primary amine
$C$. Hoffmann Bromamide reaction $3$. Reaction of phthalimide with $KOH$ and $R-X$
$D$. Carbylamine reaction $4$. Reaction of alkyl-halides with $NH_3$

$A$ nitrogen-containing organic compound gave an oily liquid on heating with bromine and potassium hydroxide solution. On shaking the product with acetic anhydride,an antipyretic drug was obtained. The reactions indicate that the starting compound is

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Write the chemical reactions for the following conversions:
$1.$ Aniline to Picric acid
$2.$ Ethanal to Butan$-2-$ol

$90 \ g$ of ethylamine on reaction with methyl chloride produces a tertiary amine as the exclusive product. The amount of methyl chloride required is:
$[\text{Given atomic masses in amu}: H=1, C=12, N=14, Cl=35.5]$ (in $g$)

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