Which of the following compounds will give a tribromo derivative upon reaction with bromine water?

  • A
    $m$-cresol
  • B
    Benzyl alcohol
  • C
    $o$-cresol
  • D
    $p$-cresol

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Similar Questions

Match List-$I$ with List-$II$ :
List-$I$ List-$II$
$A$. $H_{3}C-CH(OH)-CH_{3}$ $I$. $(i)$ oleum; (ii) $NaOH, \Delta$; (iii) $H^{+}$
$B$. $CH_{3}COOH \rightarrow CH_{3}CH_{2}OH$ $II$. $(i)$ $O_{2}$; (ii) $H_{2}O/H^{+}$
$C$. $CH_{3}CH_{2}OH \rightarrow H_{3}C-CH(OH)-CH_{3}$ $III$. $(i)$ $CH_{3}OH, H^{+}$; (ii) $H_{2}$, Catalyst
$D$. Benzene $\rightarrow$ Phenol $IV$. $(i)$ conc. $H_{2}SO_{4}, \Delta$; (ii) $H^{+}/H_{2}O$

Choose the correct answer from the options given below :

Esterification of the acid $P$ with the alcohol $Q$ will give:

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Oxalic acid + $A \rightarrow$ Glycerol monooxalate. If $A \xrightarrow{conc.\,H_2SO_4} B$,then $B$ is:

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Choose the correct option by putting $T$ for the true statement and $F$ for the false statement.
$(i)$ Phenol is more acidic as compared to ethanol.
$(ii)$ Melting point of $o$-nitrophenol is lesser than $p$-nitrophenol.
$(iii)$ Neutralization of phenol is done with $NaHCO_3$.
$(iv)$ Nucleophilic substitution reaction is taking place in the aromatic ring of phenol.

Product $(D)$ in the above reaction is:

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