The bonds to the hydrogen atoms on the inside of the [18]annulene ring are to be drawn. Whether a significant ring strain will be present in [18]annulene is to be determined. Concept introduction: An annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds. This means each ring carbon is bonded to only one hydrogen atom. Some of these hydrogen atoms are so oriented that they project inside the ring. If the ring is small or very large, the electron clouds of some of these internal hydrogen atoms tend to interfere with each other, producing a steric strain.

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Answer 1

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Chapter 14, Problem 14.9YT

Interpretation Introduction

Interpretation:

The bonds to the hydrogen atoms on the inside of the [18]annulene ring are to be drawn. Whether a significant ring strain will be present in [18]annulene is to be determined.

Concept introduction:

An annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds. This means each ring carbon is bonded to only one hydrogen atom. Some of these hydrogen atoms are so oriented that they project inside the ring. If the ring is small or very large, the electron clouds of some of these internal hydrogen atoms tend to interfere with each other, producing a steric strain.

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Answer 2

Question

Chapter 14, Problem 14.9YT

Interpretation Introduction

Interpretation:

The bonds to the hydrogen atoms on the inside of the [18]annulene ring are to be drawn. Whether a significant ring strain will be present in [18]annulene is to be determined.

Concept introduction:

An annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds. This means each ring carbon is bonded to only one hydrogen atom. Some of these hydrogen atoms are so oriented that they project inside the ring. If the ring is small or very large, the electron clouds of some of these internal hydrogen atoms tend to interfere with each other, producing a steric strain.

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Answer 3

Question

Chapter 14, Problem 14.9YT

Interpretation Introduction

Interpretation:

The bonds to the hydrogen atoms on the inside of the [18]annulene ring are to be drawn. Whether a significant ring strain will be present in [18]annulene is to be determined.

Concept introduction:

An annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds. This means each ring carbon is bonded to only one hydrogen atom. Some of these hydrogen atoms are so oriented that they project inside the ring. If the ring is small or very large, the electron clouds of some of these internal hydrogen atoms tend to interfere with each other, producing a steric strain.

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Answer 4

Question

Chapter 14, Problem 14.9YT

Interpretation Introduction

Interpretation:

The bonds to the hydrogen atoms on the inside of the [18]annulene ring are to be drawn. Whether a significant ring strain will be present in [18]annulene is to be determined.

Concept introduction:

An annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds. This means each ring carbon is bonded to only one hydrogen atom. Some of these hydrogen atoms are so oriented that they project inside the ring. If the ring is small or very large, the electron clouds of some of these internal hydrogen atoms tend to interfere with each other, producing a steric strain.

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Answer 5

Chapter 14, Problem 14.9YT

Interpretation Introduction

Interpretation:

The bonds to the hydrogen atoms on the inside of the [18]annulene ring are to be drawn. Whether a significant ring strain will be present in [18]annulene is to be determined.

Concept introduction:

An annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds. This means each ring carbon is bonded to only one hydrogen atom. Some of these hydrogen atoms are so oriented that they project inside the ring. If the ring is small or very large, the electron clouds of some of these internal hydrogen atoms tend to interfere with each other, producing a steric strain.

Answer 6

Chapter 14, Problem 14.9YT

Interpretation Introduction

Interpretation:

The bonds to the hydrogen atoms on the inside of the [18]annulene ring are to be drawn. Whether a significant ring strain will be present in [18]annulene is to be determined.

Concept introduction:

An annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds. This means each ring carbon is bonded to only one hydrogen atom. Some of these hydrogen atoms are so oriented that they project inside the ring. If the ring is small or very large, the electron clouds of some of these internal hydrogen atoms tend to interfere with each other, producing a steric strain.

Answer 7

Chapter 14, Problem 14.9YT

Interpretation Introduction

Interpretation:

The bonds to the hydrogen atoms on the inside of the [18]annulene ring are to be drawn. Whether a significant ring strain will be present in [18]annulene is to be determined.

Concept introduction:

An annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds. This means each ring carbon is bonded to only one hydrogen atom. Some of these hydrogen atoms are so oriented that they project inside the ring. If the ring is small or very large, the electron clouds of some of these internal hydrogen atoms tend to interfere with each other, producing a steric strain.

Answer 8

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Answer 11

Ch. 14 - Prob. 14.1P Ch. 14 - Prob. 14.2P Ch. 14 - Prob. 14.3P Ch. 14 - Prob. 14.4P Ch. 14 - Prob. 14.5P Ch. 14 - Prob. 14.6P Ch. 14 - Prob. 14.7P Ch. 14 - Prob. 14.8P Ch. 14 - Prob. 14.9P Ch. 14 - Prob. 14.10P

Solution Summary: The author explains that [18]annulene is a monocyclic hydrocarbon with the maximum possible number of alternating single and double bonds.

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Chapter 14 Solutions