Interpretation For the given compounds their conjugate base should be explained and it should be checked they are aromatic or not Concept introduction: Conjugate base is formed by the deprotonation of the parent acid The conditions for aromatic compound are, 1. It should be planar 2. It must obey the Huckel’s rule The requirement of an odd number of electron pair is called Huckel’s rule . A compound can only be aromatic if the number of π electron in the ring is 2, 6,10,14,18 and so on. This series of number can be expressed mathematically as 4n+2 , where n should be an integer and the compound is aromatic. 3. Continuous conjugated π system(all carbon should be in sp 2 hybridized state) A five membered ring will be aromatic if it contains six π electrons. In order to have six π electrons, one of the carbon atoms must possess two electrons. It should be a carbanion If any compound which doesn’t satisfy one of the above condition then the compound is not aromatic

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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 17, Problem 47PP

Interpretation Introduction

Interpretation For the given compounds their conjugate base should be explained and it should be checked they are aromatic or not

Concept introduction:

Conjugate base is formed by the deprotonation of the parent acid

The conditions for aromatic compound are,

1. It should be planar

2. It must obey the Huckel’s rule

The requirement of an odd number of electron pair is called Huckel’s rule. A compound can only be aromatic if the number of π electron in the ring is 2, 6,10,14,18 and so on. This series of number can be expressed mathematically as 4n+2 , where n should be an integer and the compound is aromatic.

3. Continuous conjugated π system(all carbon should be in sp2 hybridized state)

A five membered ring will be aromatic if it contains six π electrons. In order to have six π electrons, one of the carbon atoms must possess two electrons. It should be a carbanion

If any compound which doesn’t satisfy one of the above condition then the compound is not 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 47PP

Interpretation Introduction

Interpretation For the given compounds their conjugate base should be explained and it should be checked they are aromatic or not

Concept introduction:

Conjugate base is formed by the deprotonation of the parent acid

The conditions for aromatic compound are,

1. It should be planar

2. It must obey the Huckel’s rule

The requirement of an odd number of electron pair is called Huckel’s rule. A compound can only be aromatic if the number of π electron in the ring is 2, 6,10,14,18 and so on. This series of number can be expressed mathematically as 4n+2 , where n should be an integer and the compound is aromatic.

3. Continuous conjugated π system(all carbon should be in sp2 hybridized state)

A five membered ring will be aromatic if it contains six π electrons. In order to have six π electrons, one of the carbon atoms must possess two electrons. It should be a carbanion

If any compound which doesn’t satisfy one of the above condition then the compound is not aromatic

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Check out a sample textbook solution

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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 47PP

Interpretation Introduction

Interpretation For the given compounds their conjugate base should be explained and it should be checked they are aromatic or not

Concept introduction:

Conjugate base is formed by the deprotonation of the parent acid

The conditions for aromatic compound are,

1. It should be planar

2. It must obey the Huckel’s rule

The requirement of an odd number of electron pair is called Huckel’s rule. A compound can only be aromatic if the number of π electron in the ring is 2, 6,10,14,18 and so on. This series of number can be expressed mathematically as 4n+2 , where n should be an integer and the compound is aromatic.

3. Continuous conjugated π system(all carbon should be in sp2 hybridized state)

A five membered ring will be aromatic if it contains six π electrons. In order to have six π electrons, one of the carbon atoms must possess two electrons. It should be a carbanion

If any compound which doesn’t satisfy one of the above condition then the compound is not 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 47PP

Interpretation Introduction