The compounds having delocalized electrons have to be predicted. Concept Introduction: Resonance Contributor: The appropriate structure with the delocalized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure. Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds. Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.

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Answer 1

Question

Chapter 7, Problem 31P

Interpretation Introduction

Interpretation:

The compounds having delocalized electrons have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the delocalized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.

Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.

Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.

Expert Solution & Answer

Explanation of Solution

Reason for correct options:

Essential Organic Chemistry (3rd Edition), Chapter 7, Problem 31P

The above compounds all have delocalized electrons, which undergo electron movement.

The resonance structures can be drawn as shown above.

Hence, the correct options are A, B, C, E, J, K and L.

Reason for in-correct options:

The remaining compounds do not contain delocalized electrons since the conjugated system is absent.

Hence, the in-correct options are D, F, G, H, I, J, and K.

Conclusion

The compounds containing delocalized electrons were predicted.

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Answer 2

Question

Chapter 7, Problem 31P

Interpretation Introduction

Interpretation:

The compounds having delocalized electrons have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the delocalized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.

Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.

Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.

Expert Solution & Answer

Explanation of Solution

Reason for correct options:

Essential Organic Chemistry (3rd Edition), Chapter 7, Problem 31P

The above compounds all have delocalized electrons, which undergo electron movement.

The resonance structures can be drawn as shown above.

Hence, the correct options are A, B, C, E, J, K and L.

Reason for in-correct options:

The remaining compounds do not contain delocalized electrons since the conjugated system is absent.

Hence, the in-correct options are D, F, G, H, I, J, and K.

Conclusion

The compounds containing delocalized electrons were predicted.

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Answer 3

Question

Chapter 7, Problem 31P

Interpretation Introduction

Interpretation:

The compounds having delocalized electrons have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the delocalized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.

Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.

Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.

Expert Solution & Answer

Explanation of Solution

Reason for correct options:

Essential Organic Chemistry (3rd Edition), Chapter 7, Problem 31P

The above compounds all have delocalized electrons, which undergo electron movement.

The resonance structures can be drawn as shown above.

Hence, the correct options are A, B, C, E, J, K and L.

Reason for in-correct options:

The remaining compounds do not contain delocalized electrons since the conjugated system is absent.

Hence, the in-correct options are D, F, G, H, I, J, and K.

Conclusion

The compounds containing delocalized electrons were predicted.

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Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!

Answer 4

Question

Chapter 7, Problem 31P

Interpretation Introduction

Interpretation:

The compounds having delocalized electrons have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the delocalized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.

Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.

Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.

Expert Solution & Answer

Explanation of Solution

Reason for correct options:

Essential Organic Chemistry (3rd Edition), Chapter 7, Problem 31P

The above compounds all have delocalized electrons, which undergo electron movement.

The resonance structures can be drawn as shown above.

Hence, the correct options are A, B, C, E, J, K and L.

Reason for in-correct options:

The remaining compounds do not contain delocalized electrons since the conjugated system is absent.

Hence, the in-correct options are D, F, G, H, I, J, and K.

Conclusion

The compounds containing delocalized electrons were predicted.

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Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!

Answer 5

Chapter 7, Problem 31P

Interpretation Introduction

Interpretation:

The compounds having delocalized electrons have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the delocalized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.

Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.

Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.

Expert Solution & Answer

Explanation of Solution

Reason for correct options:

Essential Organic Chemistry (3rd Edition), Chapter 7, Problem 31P

The above compounds all have delocalized electrons, which undergo electron movement.

The resonance structures can be drawn as shown above.

Hence, the correct options are A, B, C, E, J, K and L.

Reason for in-correct options:

The remaining compounds do not contain delocalized electrons since the conjugated system is absent.

Hence, the in-correct options are D, F, G, H, I, J, and K.

Conclusion

The compounds containing delocalized electrons were predicted.

Answer 6

Chapter 7, Problem 31P

Interpretation Introduction

Interpretation:

The compounds having delocalized electrons have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the delocalized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.

Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.

Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.

Expert Solution & Answer

Explanation of Solution

Reason for correct options:

Essential Organic Chemistry (3rd Edition), Chapter 7, Problem 31P

The above compounds all have delocalized electrons, which undergo electron movement.

The resonance structures can be drawn as shown above.

Hence, the correct options are A, B, C, E, J, K and L.

Reason for in-correct options:

The remaining compounds do not contain delocalized electrons since the conjugated system is absent.

Hence, the in-correct options are D, F, G, H, I, J, and K.

Conclusion

The compounds containing delocalized electrons were predicted.

Answer 7

Chapter 7, Problem 31P

Interpretation Introduction

Interpretation:

The compounds having delocalized electrons have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the delocalized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.

Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.

Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.

Answer 8

Expert Solution & Answer

Explanation of Solution

Reason for correct options:

Essential Organic Chemistry (3rd Edition), Chapter 7, Problem 31P

The above compounds all have delocalized electrons, which undergo electron movement.

The resonance structures can be drawn as shown above.

Hence, the correct options are A, B, C, E, J, K and L.

Reason for in-correct options:

The remaining compounds do not contain delocalized electrons since the conjugated system is absent.

Hence, the in-correct options are D, F, G, H, I, J, and K.

Answer 9

Expert Solution & Answer

Answer 10

Expert Solution & Answer

Answer 11

Conclusion

The compounds containing delocalized electrons were predicted.

Answer 12

Ch. 7.4 - Prob. 1P Ch. 7.5 - Prob. 3P Ch. 7.6 - a. Predict the relative bond lengths of the three...Ch. 7.6 - Prob. 5P Ch. 7.6 - Prob. 6P Ch. 7.7 - Prob. 7P Ch. 7.7 - Prob. 8P Ch. 7.7 - Prob. 9P Ch. 7.7 - Prob. 10P Ch. 7.8 - Which member of each pair is the stronger acid? a....

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