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ChemistryMediumAssertion Reasoning2024 · 05 Apr Shift 1

Q41.Given below are two statements: Statement I : Nitration of benzene involves the following step - Statement II : Use of Lewis base promotes the electrophilic substitution of benzene. In the light of the above statements, choose the most appropriate answer from the options given below : JEE Main 2024 (05 Apr Shift 1) JEE Main Previous Year Paper (1) Statement I is correct but Statement II is incorrect(2) Statement I is incorrect but Statement II is correct (3) Both Statement I and Statement II are correct (4) Both Statement I and Statement II are incorrect

What This Question Tests

This question tests the understanding of the mechanism of electrophilic aromatic substitution, specifically nitration, and the general role of Lewis acids/bases in such reactions. Statement I correctly describes the formation of a sigma complex (carbocation intermediate), while Statement II incorrectly assigns a promoting role to Lewis bases in EAS reactions.

Concepts Tested

Electrophilic Aromatic Substitution mechanismNitration of benzeneRole of Lewis acids and bases

📚 NCERT Sections This Tests

7.16Explain How Does The –Oh Group Attached To A Carbon Of Benzene Ring

Chemistry Class 12 · Chapter 7

75% match

7.16 Explain how does the –OH group attached to a carbon of benzene ring activate it towards electrophilic substitution?

9.8Accomplish The Following Conversions:

Chemistry Class 12 · Chapter 9

75% match

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.

8.17Complete Each Synthesis By Giving Missing Starting Material, Reagent Or Products

Chemistry Class 12 · Chapter 8

74% match

8.17 Complete each synthesis by giving missing starting material, reagent or products