The products of the given reaction have to be predicted. Concept Introduction: Resonance Contributor: The appropriate structure with the localized 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 8, Problem 57P

Interpretation Introduction

Interpretation:

The products of the given reaction have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the localized 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

Answer to Problem 57P

Correct Answer:

The compounds A, B, C, E, F, L, M, N, and O have delocalized electrons.

Explanation of Solution

Reason for correct options:

Organic Chemistry, Chapter 8, Problem 57P

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, F, L, M, N, and O.

Reason for in-correct options:

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

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

Conclusion

The compounds containing delocalized electrons were predicted.

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3. Consider the compounds below and determine if they are aromatic, antiaromatic, or non-aromatic. In case of aromatic or anti-aromatic, please indicate number of I electrons in the respective systems. (Hint: 1. Not all lone pair electrons were explicitly drawn and you should be able to tell that the bonding electrons and lone pair electrons should reside in which hybridized atomic orbital 2. You should consider ring strain- flexibility and steric repulsion that facilitates adoption of aromaticity or avoidance of anti- aromaticity) H H N N: NH2 N Aromaticity (Circle) Aromatic Aromatic Aromatic Aromatic Aromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic nonaromatic nonaromatic nonaromatic nonaromatic nonaromatic aromatic TT electrons Me H Me Aromaticity (Circle) Aromatic Aromatic Aromatic Aromatic Aromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic nonaromatic nonaromatic nonaromatic nonaromatic nonaromatic aromatic πT electrons H HH…

A chemistry graduate student is studying the rate of this reaction: 2 HI (g) →H2(g) +12(g) She fills a reaction vessel with HI and measures its concentration as the reaction proceeds: time (minutes) [IH] 0 0.800M 1.0 0.301 M 2.0 0.185 M 3.0 0.134M 4.0 0.105 M Use this data to answer the following questions. Write the rate law for this reaction. rate = 0 Calculate the value of the rate constant k. k = Round your answer to 2 significant digits. Also be sure your answer has the correct unit symbol.

Answer 2

Question

Chapter 8, Problem 57P

Interpretation Introduction

Interpretation:

The products of the given reaction have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the localized 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

Answer to Problem 57P

Correct Answer:

The compounds A, B, C, E, F, L, M, N, and O have delocalized electrons.

Explanation of Solution

Reason for correct options:

Organic Chemistry, Chapter 8, Problem 57P

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, F, L, M, N, and O.

Reason for in-correct options:

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

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

Conclusion

The compounds containing delocalized electrons were predicted.

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Answer 3

Question

Chapter 8, Problem 57P

Interpretation Introduction

Interpretation:

The products of the given reaction have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the localized 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

Answer to Problem 57P

Correct Answer:

The compounds A, B, C, E, F, L, M, N, and O have delocalized electrons.

Explanation of Solution

Reason for correct options:

Organic Chemistry, Chapter 8, Problem 57P

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, F, L, M, N, and O.

Reason for in-correct options:

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

Hence, the in-correct options are D, 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 8, Problem 57P

Interpretation Introduction

Interpretation:

The products of the given reaction have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the localized 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

Answer to Problem 57P

Correct Answer:

The compounds A, B, C, E, F, L, M, N, and O have delocalized electrons.

Explanation of Solution

Reason for correct options:

Organic Chemistry, Chapter 8, Problem 57P

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, F, L, M, N, and O.

Reason for in-correct options:

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

Hence, the in-correct options are D, 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 8, Problem 57P

Interpretation Introduction

Interpretation:

The products of the given reaction have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the localized 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

Answer to Problem 57P

Correct Answer:

The compounds A, B, C, E, F, L, M, N, and O have delocalized electrons.

Explanation of Solution

Reason for correct options:

Organic Chemistry, Chapter 8, Problem 57P

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, F, L, M, N, and O.

Reason for in-correct options:

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

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

Conclusion

The compounds containing delocalized electrons were predicted.

Answer 6

Chapter 8, Problem 57P

Interpretation Introduction

Interpretation:

The products of the given reaction have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the localized 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

Answer to Problem 57P

Correct Answer:

The compounds A, B, C, E, F, L, M, N, and O have delocalized electrons.

Explanation of Solution

Reason for correct options:

Organic Chemistry, Chapter 8, Problem 57P

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, F, L, M, N, and O.

Reason for in-correct options:

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

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

Conclusion

The compounds containing delocalized electrons were predicted.

Answer 7

Chapter 8, Problem 57P

Interpretation Introduction

Interpretation:

The products of the given reaction have to be predicted.

Concept Introduction:

Resonance Contributor: The appropriate structure with the localized 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

Answer to Problem 57P

Correct Answer:

The compounds A, B, C, E, F, L, M, N, and O have delocalized electrons.

Answer 9

Expert Solution & Answer

Answer 10

Expert Solution & Answer

Answer 11

Explanation of Solution

Reason for correct options:

Organic Chemistry, Chapter 8, Problem 57P

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, F, L, M, N, and O.

Reason for in-correct options:

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

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

Answer 12

Conclusion

The compounds containing delocalized electrons were predicted.

Answer 13

Ch. 8.1 - Prob. 1P Ch. 8.1 - Prob. 2P Ch. 8.4 - Prob. 3P Ch. 8.5 - Prob. 5P Ch. 8.6 - a. Predict the relative bond lengths of the three...Ch. 8.6 - Prob. 7P Ch. 8.6 - Prob. 8P Ch. 8.8 - Prob. 9P Ch. 8.9 - Prob. 10P Ch. 8.9 - Prob. 12P

Concept explainers

Answer to Problem 57P

Explanation of Solution

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Chapter 8 Solutions