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.

Explore More

Similar Questions

The order of reactivity of phenol $(I)$,nitrobenzene $(II)$,and benzene $(III)$ towards nitration is:

Which of the following compounds reacts with ethylmagnesium bromide and also decolourizes bromine water solution?

When carbolic acid is heated with concentrated nitric acid in the presence of concentrated sulphuric acid,it forms:

The products $X$ and $Y$ which are formed in the following sequence of reactions are respectively:
$\text{Phenol}$ $\xrightarrow{dil \ HNO_3} X$ $\xrightarrow{1. Zn/HCl, \Delta \atop 2.(CH_3CO)_2O (1 \ equiv)} Y$

Which among the following is a dihydric phenol?

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo