Organic Chemistry
Organic Chemistry
3rd Edition
ISBN: 9781119316152
Author: Klein, David R.
Publisher: WILEY
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Chapter 2.9, Problem 17ATS

(a)

Interpretation Introduction

Interpretation:

Curved arrows needed to convert the resonance structure 2a into 2b have to be drawn.

Concept Introduction:

The unshared electrons are called lone pair.

A negative charge means two lone pairs means and a positive charge means one lone pair

Curved arrows are necessary in drawing the resonance structure.

Curved arrows has a head indicating that the electrons are coming and tail indicating that the electrons are going.

The two rules in drawing the resonance structure is,

  • Breaking of single bond is not allowed.
  • Never exceed an octet for second row elements.

When a single Lewis structure does not represent a structure adequately, the true structure is the intermediate between the two or more structure referred to as resonance structure.

(b)

Interpretation Introduction

Interpretation:

Curved arrows needed to convert the resonance structure 2a into 2c have to be drawn.

Concept Introduction:

The unshared electrons are called lone pair.

A negative charge means two lone pairs means and a positive charge means one lone pair

Curved arrows are necessary in drawing the resonance structure.

Curved arrows has a head indicating that the electrons are coming and tail indicating that the electrons are going.

The two rules in drawing the resonance structure is,

  • Breaking of single bond is not allowed.
  • Never exceed an octet for second row elements.

When a single Lewis structure does not represent a structure adequately, the true structure is the intermediate between the two or more structure referred to as resonance structure.

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Chapter 2 Solutions

Organic Chemistry

Ch. 2.5 - Prob. 4LTSCh. 2.5 - Prob. 8PTSCh. 2.5 - The rich and varied flavors of toasted bread,...Ch. 2.5 - Prob. 5LTSCh. 2.5 - Prob. 10PTSCh. 2.5 - Prob. 11ATSCh. 2.8 - Prob. 6LTSCh. 2.8 - Prob. 12PTSCh. 2.8 - Prob. 13PTSCh. 2.8 - Prob. 14ATSCh. 2.9 - Prob. 7LTSCh. 2.9 - Prob. 15PTSCh. 2.9 - Prob. 16PTSCh. 2.9 - The cation 1 has been shown to lose a proton (H+)...Ch. 2.10 - Prob. 18CCCh. 2.10 - Prob. 19CCCh. 2.10 - Prob. 20CCCh. 2.10 - Prob. 21CCCh. 2.10 - Prob. 22CCCh. 2.10 - Prob. 23CCCh. 2.10 - Prob. 24CCCh. 2.10 - Prob. 25CCCh. 2.11 - Prob. 8LTSCh. 2.11 - Prob. 26PTSCh. 2.11 - Prob. 27ATSCh. 2.11 - Prob. 28ATSCh. 2.12 - Prob. 9LTSCh. 2.12 - Prob. 29PTSCh. 2.12 - The dragmacidin class of natural products has been...Ch. 2.13 - Prob. 10LTSCh. 2.13 - Prob. 31PTSCh. 2.13 - Prob. 32ATSCh. 2.13 - Prob. 33ATSCh. 2 - Prob. 34PPCh. 2 - Prob. 35PPCh. 2 - Prob. 36PPCh. 2 - Prob. 37PPCh. 2 - Prob. 38PPCh. 2 - Prob. 39PPCh. 2 - Prob. 40PPCh. 2 - Prob. 41PPCh. 2 - Prob. 42PPCh. 2 - Prob. 43PPCh. 2 - Prob. 44PPCh. 2 - Amino acids are biological compounds with the...Ch. 2 - Prob. 46PPCh. 2 - Prob. 47PPCh. 2 - Prob. 48PPCh. 2 - Prob. 49PPCh. 2 - Prob. 50PPCh. 2 - Prob. 51PPCh. 2 - Prob. 52PPCh. 2 - Prob. 53PPCh. 2 - Prob. 54PPCh. 2 - Prob. 55PPCh. 2 - Prob. 56PPCh. 2 - Prob. 57PPCh. 2 - Prob. 58PPCh. 2 - Prob. 59PPCh. 2 - Prob. 60PPCh. 2 - Prob. 61PPCh. 2 - Prob. 62PPCh. 2 - Enamines, compounds with an amino group attached...Ch. 2 - Prob. 64IPCh. 2 - Ramelteon is a hypnotic agent used in the...Ch. 2 - Prob. 66IPCh. 2 - Prob. 67IPCh. 2 - Prob. 68IPCh. 2 - The natural products 3 and 4 have similar core...Ch. 2 - Prob. 70IPCh. 2 - Prob. 71IPCh. 2 - Prob. 72IPCh. 2 - Prob. 73IPCh. 2 - Prob. 74IPCh. 2 - Prob. 75IPCh. 2 - Coumarin and its derivatives exhibit a broad array...Ch. 2 - Prob. 77IPCh. 2 - Prob. 78IPCh. 2 - Prob. 79IPCh. 2 - Prob. 80IPCh. 2 - Prob. 81CPCh. 2 - Prob. 82CPCh. 2 - Prob. 83CPCh. 2 - Prob. 84CP
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