Consider the following reactions:C_6H_5N_2Cl | vedclass

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(A) $1$. The reaction of benzenediazonium chloride $(C_6H_5N_2Cl)$ with water at $283 \ K$ yields phenol $(X)$.$2$. Phenol $(X)$ reacts with concentra

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Picric acid ($2,4,6-$Trinitrophenol),$2,4,6-$Tribromophenol

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(A) $1$. The reaction of benzenediazonium chloride $(C_6H_5N_2Cl)$ with water at $283 \ K$ yields phenol $(X)$.$2$. Phenol $(X)$ reacts with concentrated $HNO_3$ to undergo electrophilic aromatic substitution,resulting in the formation of $2,4,6-$trinitrophenol,also known as picric acid $(Y)$.$3$. Phenol $(X)$ reacts with bromine water $(Br_2/H_2O)$ to undergo rapid electrophilic substitution at all available ortho and para positions,yielding $2,4,6-$tribromophenol $(Z)$.

Consider the following reactions:
$C_6H_5N_2Cl$ $\xrightarrow{H_2O, 283 \ K} X$ $\xrightarrow{Conc. \ HNO_3} Y$
$X \xrightarrow{Br_2/H_2O} Z$
$Y$ and $Z$ respectively are:

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Consider the following reactions:$C_6H_5N_2Cl$ $\xrightarrow{H_2O, 283 \ K} X$ $\xrightarrow{Conc. \ HNO_3} Y$$X \xrightarrow{Br_2/H_2O} Z$$Y$ and $Z$ respectively are: