Which of the following reactions involves the formation of a carbene intermediate?

  • A
    Reimer-Tiemann reaction
  • B
    Carbylamine reaction
  • C
    Hoffmann bromamide reaction
  • D
    Both $A$ and $B$

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Which of the following compounds does not form phenol or phenoxide upon reaction under standard laboratory conditions?

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Match each of the compounds given in Column $I$ with the reaction$(s)$ that they can undergo,given in Column $II$.
| Column $I$ | Column $II$ |
| :--- | :--- |
| $(A)$ $3-$bromobenzofuran derivative | $(p)$ Nucleophilic substitution |
| $(B)$ Benzyl alcohol | $(q)$ Elimination |
| $(C)$ Salicylaldehyde | $(r)$ Nucleophilic addition |
| $(D)$ $1-$bromo$-2-$nitrobenzene | $(s)$ Esterification with acetic anhydride |
| | $(t)$ Dehydrogenation |

Scheme $1$ and $2$ describe the conversion of $P$ to $Q$ and $R$ to $S$,respectively. Scheme $3$ describes the synthesis of $T$ from $Q$ and $S$. The total number of $Br$ atoms in a molecule of $T$ is. . . . . . . .

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