(a) Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic. Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4 n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule. According to the Huckel’s rule the number of π electrons in the molecule must be equal to ( 4 n + 2 ) .

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Answer 1

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Definition Definition Rule that estimates whether a given organic planar ring structure will show an aromatic property. A cyclic ring molecule is said to follow Hückel’s rule if the л-electrons count in a molecule is [4n+2], where n stands for a positive numerical value. It is also called the [4n+2] rule. Hückel's rule, sometimes referred to as the aromaticity rule, is one but not the only criteria to judge a molecule for aromaticity.

Chapter 15, Problem 21P

Interpretation Introduction

(a)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(b)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(c)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

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Answer 2

Question

Definition Definition Rule that estimates whether a given organic planar ring structure will show an aromatic property. A cyclic ring molecule is said to follow Hückel’s rule if the л-electrons count in a molecule is [4n+2], where n stands for a positive numerical value. It is also called the [4n+2] rule. Hückel's rule, sometimes referred to as the aromaticity rule, is one but not the only criteria to judge a molecule for aromaticity.

Chapter 15, Problem 21P

Interpretation Introduction

(a)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(b)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(c)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

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Answer 3

Question

Definition Definition Rule that estimates whether a given organic planar ring structure will show an aromatic property. A cyclic ring molecule is said to follow Hückel’s rule if the л-electrons count in a molecule is [4n+2], where n stands for a positive numerical value. It is also called the [4n+2] rule. Hückel's rule, sometimes referred to as the aromaticity rule, is one but not the only criteria to judge a molecule for aromaticity.

Chapter 15, Problem 21P

Interpretation Introduction

(a)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(b)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(c)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

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Answer 4

Question

Definition Definition Rule that estimates whether a given organic planar ring structure will show an aromatic property. A cyclic ring molecule is said to follow Hückel’s rule if the л-electrons count in a molecule is [4n+2], where n stands for a positive numerical value. It is also called the [4n+2] rule. Hückel's rule, sometimes referred to as the aromaticity rule, is one but not the only criteria to judge a molecule for aromaticity.

Chapter 15, Problem 21P

Interpretation Introduction

(a)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(b)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(c)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

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Answer 5

Chapter 15, Problem 21P

Interpretation Introduction

(a)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(b)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Interpretation Introduction

(c)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Answer 6

Chapter 15, Problem 21P

Interpretation Introduction

(a)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Answer 7

Chapter 15, Problem 21P

Interpretation Introduction

(a)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Answer 8

Interpretation Introduction

(b)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Answer 9

Interpretation Introduction

(b)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Answer 10

Interpretation Introduction

(c)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Answer 11

Interpretation Introduction

(c)

Interpretation: The given compound is to be classified as aromatic, antiaromatic or not aromatic.

Concept introduction: A molecule must be cyclic, planar, completely conjugated and should follow Huckel’s rule to be classified as aromatic. For an antiaromatic molecule, the molecule must be cyclic, planar, completely conjugated and have 4n π electrons. For a non-aromatic molecule, the molecule lacks the one of the requirements to be aromatic or anti aromatic molecule.

According to the Huckel’s rule the number of π electrons in the molecule must be equal to (4n+2).

Answer 12

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Answer 13

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Answer 14

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Answer 15

Ch. 15.2 - Prob. 1P Ch. 15.2 - Problem 17.2 What orbitals are used to form the...Ch. 15.3 - Prob. 4P Ch. 15.3 - Problem-17.5 What is the structure of propofol,...Ch. 15.6 - Prob. 7P Ch. 15.8 - Prob. 8P Ch. 15.8 - Prob. 11P Ch. 15.8 - Prob. 12P Ch. 15.8 - Problem 17.16 Rank the following compounds in...Ch. 15.8 - Problem 17.17 Draw the seven resonance structures...

Solution Summary: The author explains that a molecule must be cyclic, planar, completely conjugated and follow Huckel's rule to be classified as aromatic.

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