Structure of the complex formed by 1,2,5,6-tetracyanocyclooctatetraene and M g + · has to be sketched where dotted lines is used to show the interaction between lone pairs and M g + · . Concept Introduction: Huckel’s rule states that based on the number of pi electrons planar, monocyclic, and conjugated polyene compounds can be classified as aromatic or anti-aromatic. a) The number of π electrons in a cyclic conjugated system is 4 n where n is an integer, then it is antiaromatic. b) The number of π electrons in a cyclic conjugated system is ( 4 n + 2 ) where n is an integer, then it is aromatic.

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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 17, Problem 64IP

(a)

Interpretation Introduction

Interpretation: Structure of the complex formed by 1,2,5,6-tetracyanocyclooctatetraene and Mg+· has to be sketched where dotted lines is used to show the interaction between lone pairs and Mg+·.

Concept Introduction:

Huckel’s rule states that based on the number of pi electrons planar, monocyclic, and conjugated polyene compounds can be classified as aromatic or anti-aromatic.

a) The number of π electrons in a cyclic conjugated system is 4n where n is an integer, then it is antiaromatic.

b) The number of π electrons in a cyclic conjugated system is (4n+2) where n is an integer, then it is aromatic.

(b)

Interpretation Introduction

Interpretation: Reason for why 1,2,4,5-tetracyanobenzene does not make a complex with Mg+· has to be explained.

Concept Introduction:

Huckel’s rule states that based on the number of pi electrons planar, monocyclic, and conjugated polyene compounds can be classified as aromatic or anti-aromatic.

a) The number of π electrons in a cyclic conjugated system is 4n where n is an integer, then it is antiaromatic.

b) The number of π electrons in a cyclic conjugated system is (4n+2) where n is an integer, then it is aromatic.

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Answer 2

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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 17, Problem 64IP

(a)

Interpretation Introduction

Interpretation: Structure of the complex formed by 1,2,5,6-tetracyanocyclooctatetraene and Mg+· has to be sketched where dotted lines is used to show the interaction between lone pairs and Mg+·.

Concept Introduction:

Huckel’s rule states that based on the number of pi electrons planar, monocyclic, and conjugated polyene compounds can be classified as aromatic or anti-aromatic.

a) The number of π electrons in a cyclic conjugated system is 4n where n is an integer, then it is antiaromatic.

b) The number of π electrons in a cyclic conjugated system is (4n+2) where n is an integer, then it is aromatic.

(b)

Interpretation Introduction

Interpretation: Reason for why 1,2,4,5-tetracyanobenzene does not make a complex with Mg+· has to be explained.

Concept Introduction:

Huckel’s rule states that based on the number of pi electrons planar, monocyclic, and conjugated polyene compounds can be classified as aromatic or anti-aromatic.

a) The number of π electrons in a cyclic conjugated system is 4n where n is an integer, then it is antiaromatic.

b) The number of π electrons in a cyclic conjugated system is (4n+2) where n is an integer, then it is aromatic.

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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 17, Problem 64IP

(a)

Interpretation Introduction

Interpretation: Structure of the complex formed by 1,2,5,6-tetracyanocyclooctatetraene and Mg+· has to be sketched where dotted lines is used to show the interaction between lone pairs and Mg+·.

Concept Introduction:

Huckel’s rule states that based on the number of pi electrons planar, monocyclic, and conjugated polyene compounds can be classified as aromatic or anti-aromatic.

a) The number of π electrons in a cyclic conjugated system is 4n where n is an integer, then it is antiaromatic.

b) The number of π electrons in a cyclic conjugated system is (4n+2) where n is an integer, then it is aromatic.

(b)

Interpretation Introduction

Interpretation: Reason for why 1,2,4,5-tetracyanobenzene does not make a complex with Mg+· has to be explained.

Concept Introduction:

Huckel’s rule states that based on the number of pi electrons planar, monocyclic, and conjugated polyene compounds can be classified as aromatic or anti-aromatic.

a) The number of π electrons in a cyclic conjugated system is 4n where n is an integer, then it is antiaromatic.

b) The number of π electrons in a cyclic conjugated system is (4n+2) where n is an integer, then it is aromatic.

Expert Solution & Answer

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Check out a sample textbook solution

See solution

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 17, Problem 64IP

(a)

Interpretation Introduction