ORG CHEM CONNECT CARD
ORG CHEM CONNECT CARD
6th Edition
ISBN: 9781264860746
Author: SMITH
Publisher: MCG
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Chapter 13, Problem 40P
Interpretation Introduction

(a)

Interpretation: The resonance structures of given radical are to be drawn.

Concept introduction: The delocalization of lone pair or free electrons from one place to another is known as resonance. The stability of compound depends upon the number of resonating structures. More the resonating structures of compound more will its stability.

Interpretation Introduction

(b)

Interpretation: The resonance structures of given radical are to be drawn.

Concept introduction: The delocalization of lone pair or free electrons from one place to another is known as resonance. The stability of compound depends upon the number of resonating structures. More the resonating structures of compound more will its stability.

Interpretation Introduction

(c)

Interpretation: The resonance structures of given radical are to be drawn.

Concept introduction: The delocalization of lone pair or free electrons from one place to another is known as resonance. The stability of compound depends upon the number of resonating structures. More the resonating structures of compound more will its stability.

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Students have asked these similar questions
Label each compound as aromatic, antiaromatic, or not aromatic. Assume all completely conjugated rings are planar. Å a. b. C. d.
a.Draw all reasonable resonance structures for pyrrole, and explain why pyrrole is less resonance stabilized than benzene. b.Draw all reasonable resonance structures for furan, and explain why furan is less resonance stabilized than pyrrole.
Draw a second resonance structure for each carbocation. Then draw the hybrid.
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