The more basic amine compound has to be found for the given pairs of compounds Concept Introduction : If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character. To find: Decide the more basic amine compound in the given pairs of compounds (a) Get a compound where lone pairs on nitrogen atoms are delocalized

Question

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Answer 1

Question

Chapter 22.3, Problem 6CC

(a)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (a)

Get a compound where lone pairs on nitrogen atoms are delocalized

(b)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (b)

Get a compound where lone pairs on nitrogen atoms are delocalized

(c)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (c)

Get a compound where lone pairs on nitrogen atoms are delocalized

(d)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (d)

Get a compound where lone pairs on nitrogen atoms are delocalized

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Answer 2

Question

Chapter 22.3, Problem 6CC

(a)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (a)

Get a compound where lone pairs on nitrogen atoms are delocalized

(b)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (b)

Get a compound where lone pairs on nitrogen atoms are delocalized

(c)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (c)

Get a compound where lone pairs on nitrogen atoms are delocalized

(d)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (d)

Get a compound where lone pairs on nitrogen atoms are delocalized

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 22.3, Problem 6CC

(a)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (a)

Get a compound where lone pairs on nitrogen atoms are delocalized

(b)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (b)

Get a compound where lone pairs on nitrogen atoms are delocalized

(c)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (c)

Get a compound where lone pairs on nitrogen atoms are delocalized

(d)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (d)

Get a compound where lone pairs on nitrogen atoms are delocalized

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 22.3, Problem 6CC

(a)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (a)

Get a compound where lone pairs on nitrogen atoms are delocalized

(b)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (b)

Get a compound where lone pairs on nitrogen atoms are delocalized

(c)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (c)

Get a compound where lone pairs on nitrogen atoms are delocalized

(d)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (d)

Get a compound where lone pairs on nitrogen atoms are delocalized

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 22.3, Problem 6CC

(a)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (a)

Get a compound where lone pairs on nitrogen atoms are delocalized

(b)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (b)

Get a compound where lone pairs on nitrogen atoms are delocalized

(c)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (c)

Get a compound where lone pairs on nitrogen atoms are delocalized

(d)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (d)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 6

Chapter 22.3, Problem 6CC

(a)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (a)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 7

Chapter 22.3, Problem 6CC

(a)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (a)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 8

(b)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (b)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 9

(b)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (b)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 10

(c)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (c)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 11

(c)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (c)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 12

(d)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (d)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 13

(d)

Interpretation Introduction

Interpretation: The more basic amine compound has to be found for the given pairs of compounds

Concept Introduction:

If the lone pair of electrons on nitrogen atom in amine compound is delocalized, that compound is resonance stabilized. It is also involved in aromatic stabilization. As a result, a number of resonance structures are drawn for the delocalization of electrons in the structures. So, the compound has less basic character. If the lone pair of electrons on nitrogen atom in amine compound is localized, that compound doesn’t involve in resonance stabilization. So, that compound has more basic character.

To find: Decide the more basic amine compound in the given pairs of compounds (d)

Get a compound where lone pairs on nitrogen atoms are delocalized

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

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Check out a sample textbook solution

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Answer 17

Ch. 22.2 - Prob. 1LTS Ch. 22.2 - Prob. 1PTS Ch. 22.2 - Prob. 2PTS Ch. 22.3 - Prob. 4CC Ch. 22.3 - Prob. 5CC Ch. 22.3 - Prob. 6CC Ch. 22.3 - Prob. 7CC Ch. 22.3 - Prob. 8CC Ch. 22.3 - Prob. 9CC Ch. 22.4 - Prob. 10CC

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Chapter 22 Solutions