Q37.In the following reaction, the reason why meta-nitro product also formed is: (1) Formation of anilinium ion (2) -NH2 group is highly meta-directive (3) -NO2 substitution always takes place at meta- (4) low temperature position
What This Question Tests
This question explains the formation of meta-nitroaniline during the nitration of aniline, attributing it to the protonation of the amino group in acidic medium to form the meta-directing anilinium ion.
Concepts Tested
📚 NCERT Sections This Tests
9.8 — Accomplish The Following Conversions:
Chemistry Class 12 · Chapter 9
9.8 Accomplish the following conversions: (i) Nitrobenzene to benzoic acid (ii) Benzene to m-bromophenol (iii) Benzoic acid to aniline (iv) Aniline to 2,4,6-tribromofluorobenzene (v) Benzyl chloride to 2-phenylethanamine (vi) Chlorobenzene to p-chloroaniline (vii) Aniline to p-bromoaniline (viii) Benzamide to toluene (ix) Aniline to benzyl alcohol.
7.16 — Explain How Does The –Oh Group Attached To A Carbon Of Benzene Ring
Chemistry Class 12 · Chapter 7
7.16 Explain how does the –OH group attached to a carbon of benzene ring activate it towards electrophilic substitution?
7.8 — Ortho And Para Nitrophenols Are More Acidic Than Phenol. Draw The
Chemistry Class 12 · Chapter 7
7.8 Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.
📋 Question Details
- Chapter
- Nitrogen Compounds
- Topic
- Nitration of Aniline
- Year
- 2021
- Shift
- 24 Feb Shift 1
- Q Number
- Q37
- Type
- MCQ
- NCERT Ref
- Class 12 Chemistry Ch 13: Amines
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