When phenol is treated with $PCl_5$,the yield of chlorobenzene is generally poor because of the formation of
- ABenzoyl chloride
- B$p-chlorophenol$
- C$o-chlorophenol$
- DTriphenyl phosphate
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Similar Questions
Which of the following is $\underline{\text{NOT}}$ a dihydric phenol?
What is the common name of $Benzene-1,3-diol$?
Match the reaction in Column-$I$ with the product in Column-$II$.
Column-$I$ (Reaction) Column-$II$ (Product) $(A)$ Dinitration of $4$-methylphenol $(i)$ $2$-nitro-$4$-methylphenol + $2$-nitro-$5$-methylphenol $(B)$ Mononitration of phenyl ethanoate $(ii)$ $2,4$-dinitro-$5$-methylphenol $(C)$ Dinitration of $3$-methylphenol $(iii)$ $4$-nitrophenyl ethanoate $(D)$ Mononitration of $3$-methylphenol $(iv)$ $2,6$-dinitro-$4$-methylphenol
| Column-$I$ (Reaction) | Column-$II$ (Product) |
|---|---|
| $(A)$ Dinitration of $4$-methylphenol | $(i)$ $2$-nitro-$4$-methylphenol + $2$-nitro-$5$-methylphenol |
| $(B)$ Mononitration of phenyl ethanoate | $(ii)$ $2,4$-dinitro-$5$-methylphenol |
| $(C)$ Dinitration of $3$-methylphenol | $(iii)$ $4$-nitrophenyl ethanoate |
| $(D)$ Mononitration of $3$-methylphenol | $(iv)$ $2,6$-dinitro-$4$-methylphenol |
Medium
View SolutionIn Kolbe's reaction,instead of phenol,the phenoxide ion is treated with carbon dioxide. Why?
Medium
View SolutionIdentify the product $A$ obtained in the following reaction.
$\text{Phenol} + \text{Conc. Nitric acid} \xrightarrow{\text{conc. } H_2SO_4} A$
$\text{Phenol} + \text{Conc. Nitric acid} \xrightarrow{\text{conc. } H_2SO_4} A$
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