Given below are two statements:
Statement $I$: The acidic strength of monosubstituted nitrophenol is higher than phenol because of the electron-withdrawing nitro group.
Statement $II$: $o$-nitrophenol,$m$-nitrophenol,and $p$-nitrophenol will have the same acidic strength as they have one nitro group attached to the phenolic ring.
In the light of the above statements,choose the most appropriate answer from the options given below:

  • A
    Both Statement $I$ and Statement $II$ are incorrect.
  • B
    Statement $I$ is correct but Statement $II$ is incorrect.
  • C
    Statement $I$ is incorrect but Statement $II$ is correct.
  • D
    Both Statement $I$ and Statement $II$ are correct.

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Similar Questions

The following reaction sequence is given:
Phenol $\xrightarrow{NaOH} X$ $\xrightarrow[(ii) H^+]{(i) CO_2} Y$ $\xrightarrow{(CH_3CO)_2O/H^+} Z + CH_3COOH$
The correct statements about $Z$ from the following are:
$I$. It is $o$-hydroxybenzoic acid.
$II$. It is a non-narcotic analgesic.
$III$. It acts as antipyretic.
$IV$. It acts as antihistamine.

Salicylic acid is prepared from phenol by:

Match the following reactions of phenol with their products:

Picric acid is

Assertion : Resorcinol turns $FeCl_3$ solution purple.
Reason : Resorcinol has a phenolic group.

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