The [ 10 ] annulene given in section 14.7 B is not aromatic . The factor that makes the given 10 π − electron system aromatic is to identified. Concept introduction: Annulenes belong to the class of monocyclic compounds and are represented by the structure containing alternating single and double bonds. For an annulene to be aromatic, the molecule should have ( 4 n + 2 ) π electrons and a planer carbon skeleton.

Question

Want to see the full answer?

Answer 1

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 14, Problem 25P

Interpretation Introduction

Interpretation:

The [10] annulene given in section 14.7 B is not aromatic. The factor that makes the given 10 π−electron system aromatic is to identified.

Concept introduction:

Annulenes belong to the class of monocyclic compounds and are represented by the structure containing alternating single and double bonds.

For an annulene to be aromatic, the molecule should have (4n+2)π electrons and a planer carbon skeleton.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Why is benzene less reactive toward electrophiles than an alkene, even though it has more π electrons than an alkene (six versus two)?

Please explain Frost Circles for aromatic systems and how they can be used to explain the stability of aromatic systems and the instability of anti-aromatic systems.

Show the procedure for Naming Aromatic Rings as Substituents ?

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 14, Problem 25P

Interpretation Introduction

Interpretation:

The [10] annulene given in section 14.7 B is not aromatic. The factor that makes the given 10 π−electron system aromatic is to identified.

Concept introduction:

Annulenes belong to the class of monocyclic compounds and are represented by the structure containing alternating single and double bonds.

For an annulene to be aromatic, the molecule should have (4n+2)π electrons and a planer carbon skeleton.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

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 14, Problem 25P

Interpretation Introduction

Interpretation:

The [10] annulene given in section 14.7 B is not aromatic. The factor that makes the given 10 π−electron system aromatic is to identified.

Concept introduction:

Annulenes belong to the class of monocyclic compounds and are represented by the structure containing alternating single and double bonds.

For an annulene to be aromatic, the molecule should have (4n+2)π electrons and a planer carbon skeleton.

Expert Solution & Answer

Want to see the full answer?

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 14, Problem 25P

Interpretation Introduction