Q48.Which one of the following gives the most stable Diazonium salt ? JEE Main 2021 (01 Sep Shift 2) JEE Main Previous Year Paper (1) (2) (3) (4)
What This Question Tests
This question assesses the knowledge of factors influencing the stability of aromatic diazonium salts, primarily the role of electron-donating and electron-withdrawing groups on the aromatic ring through resonance and inductive effects.
Concepts Tested
📚 NCERT Sections This Tests
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.
7.16 — Explain How Does The –Oh Group Attached To A Carbon Of Benzene Ring
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7.16 Explain how does the –OH group attached to a carbon of benzene ring activate it towards electrophilic substitution?
9.7 — Write Short Notes On The Following:
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9.7 Write short notes on the following: (i) Carbylamine reaction (ii) Diazotisation (iii) Hofmann’s bromamide reaction (iv) Coupling reaction (v) Ammonolysis (vi) Acetylation (vii) Gabriel phthalimide synthesis.
📋 Question Details
- Chapter
- Nitrogen Compounds
- Topic
- Stability of Diazonium salts
- Year
- 2021
- Shift
- 01 Sep Shift 2
- Q Number
- Q48
- Type
- MCQ
- NCERT Ref
- Class 12 Chemistry Ch 13: Nitrogen Compounds
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