Given below are two statements:
Statement I:
The acidic strength of monosubstituted nitrophenol is higher than phenol because of electron withdrawing nitro group.
Statement II:
o-nitrophenol, m-nitrophenol and p-nitrophenol will have 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:
Given below are two statements:
Statement I:
The acidic strength of monosubstituted nitrophenol is higher than phenol because of electron withdrawing nitro group.
Statement II:
o-nitrophenol, m-nitrophenol and p-nitrophenol will have 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:
Option 1 -
Both Statement I and Statement II are correct.
Option 2 -
Both Statement I and Statement II are incorrect.
Option 3 -
Statement I is correct but Statement II is incorrect.
Option 4 -
Statement I is incorrect but Statement II is correct
Similar Questions for you
From BF3 to BI3 Lewis acidic strength increases
F2 is the strongest oxidising agent
HClO4 is the most acidic compound.
Proteins on hydrolysis gives α-amino acid because α-amino acids are building block of proteins. It is also fact that amino acids contain both –NH2 and –COOH group.
Taking an Exam? Selecting a College?
Get authentic answers from experts, students and alumni that you won't find anywhere else
Sign Up on ShikshaOn Shiksha, get access to
- 65k Colleges
- 1.2k Exams
- 688k Reviews
- 1800k Answers