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

For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. ? NH2 MgBr Will the first product that forms in this reaction create a new CC bond? ○ Yes ○ No MgBr ? Will the first product that forms in this reaction create a new CC bond? O Yes O No Click and drag to start drawing a structure. :☐ G x c olo Ar HE

Predicting As the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C - C bond as its major product: H₂N O H 1. ? 2. H3O+ If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. 0 If the major products of this reaction won't have a new CC bond, just check the box under the drawing area and leave it blank. فا Explanation Check Click and drag to start drawing a structure.

Highlight the chirality (or stereogenic) center(s) in the given compound. A compound may have one or more stereogenic centers. OH OH OH OH OH OH

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