The more stable compound out of indole and isoindole is to be identified and the reason for it is to be explained. Concept introduction: For a species to be aromatic , the number of π electrons in conjugated, planar, monocyclic species must be equal to 4 n + 2 , where n is an integer. This is called Huckel’s rule. The species which satisfies the rules for aromaticity is considered to be more stable than the species which does not satisfy these rules.

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 12.21, Problem 29P

Interpretation Introduction

Interpretation:

The more stable compound out of indole and isoindole is to be identified and the reason for it is to be explained.

Concept introduction:

For a species to be aromatic, the number of π electrons in conjugated, planar, monocyclic species must be equal to 4n+2, where n is an integer. This is called Huckel’s rule.

The species which satisfies the rules for aromaticity is considered to be more stable than the species which does not satisfy these rules.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Explain the following giving a reason in each case Why is an alkylamine more basic than ammonia? Why do primary amines have higher boiling points than the tertiary amines?

Explain why m-nitroaniline is a stronger base than p-nitroaniline.

In the 1880's, Acetanilide, sold under the name Antifebrin, was widely used as a pain reliever and fever reducer. However, it had many adverse side effects, including cyanosis as a result of methemoglobinemia. The toxic side effects were the result of a small portion of acetanilide being hydrolyzed to aniline. Acetanilide was discontinued and replaced with phenacetin. Later studies show that both acetanilide and phenacetin are metabolized to acetaminophen. This metabolite, which we know as Tylenol, is responsible for the analgesic and antipyretic properties. Part 1: Show a detailed arrow pushing mechanism of the acid catalyzed hydrolysis of acetanilide to aniline Part 2: Propose a synthesis of Acetaminophen from phenol NH NH NH Phenacetin inophen Acetanilide Attach File Browse Local Files Browse Content Collection

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 12.21, Problem 29P

Interpretation Introduction

Interpretation:

The more stable compound out of indole and isoindole is to be identified and the reason for it is to be explained.

Concept introduction:

For a species to be aromatic, the number of π electrons in conjugated, planar, monocyclic species must be equal to 4n+2, where n is an integer. This is called Huckel’s rule.

The species which satisfies the rules for aromaticity is considered to be more stable than the species which does not satisfy these rules.

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 12.21, Problem 29P

Interpretation Introduction

Interpretation:

The more stable compound out of indole and isoindole is to be identified and the reason for it is to be explained.

Concept introduction:

For a species to be aromatic, the number of π electrons in conjugated, planar, monocyclic species must be equal to 4n+2, where n is an integer. This is called Huckel’s rule.

The species which satisfies the rules for aromaticity is considered to be more stable than the species which does not satisfy these rules.

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 12.21, Problem 29P

Interpretation Introduction