The resonance contributing structure of the thymine is to be drawn. The evidence that supports the statement that the thymine follows the Hückel’s rule is to be explained. Concept introduction: A molecule that is cyclic, planar, completely conjugated and follows Huckel’s rule is classified as an aromatic compound. Aromatic compounds follow Huckel’s rule of ( 4 n + 2 ) π electrons. A ring that contains six or ten π electrons acts as an aromatic ring. The stability of a compound depends upon the number of resonating structures.

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Answer 1

Question

Chapter 20.12, Problem 19P

Interpretation Introduction

Interpretation:

The resonance contributing structure of the thymine is to be drawn. The evidence that supports the statement that the thymine follows the Hückel’s rule is to be explained.

Concept introduction:

A molecule that is cyclic, planar, completely conjugated and follows Huckel’s rule is classified as an aromatic compound.

Aromatic compounds follow Huckel’s rule of (4n+2)π electrons.

A ring that contains six or ten π electrons acts as an aromatic ring.

The stability of a compound depends upon the number of resonating structures.

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Answer 2

Question

Chapter 20.12, Problem 19P

Interpretation Introduction

Interpretation:

The resonance contributing structure of the thymine is to be drawn. The evidence that supports the statement that the thymine follows the Hückel’s rule is to be explained.

Concept introduction:

A molecule that is cyclic, planar, completely conjugated and follows Huckel’s rule is classified as an aromatic compound.

Aromatic compounds follow Huckel’s rule of (4n+2)π electrons.

A ring that contains six or ten π electrons acts as an aromatic ring.

The stability of a compound depends upon the number of resonating structures.

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Answer 3

Question

Chapter 20.12, Problem 19P

Interpretation Introduction

Interpretation:

The resonance contributing structure of the thymine is to be drawn. The evidence that supports the statement that the thymine follows the Hückel’s rule is to be explained.

Concept introduction:

A molecule that is cyclic, planar, completely conjugated and follows Huckel’s rule is classified as an aromatic compound.

Aromatic compounds follow Huckel’s rule of (4n+2)π electrons.

A ring that contains six or ten π electrons acts as an aromatic ring.

The stability of a compound depends upon the number of resonating structures.

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Answer 4

Question

Chapter 20.12, Problem 19P

Interpretation Introduction

Interpretation:

The resonance contributing structure of the thymine is to be drawn. The evidence that supports the statement that the thymine follows the Hückel’s rule is to be explained.

Concept introduction:

A molecule that is cyclic, planar, completely conjugated and follows Huckel’s rule is classified as an aromatic compound.

Aromatic compounds follow Huckel’s rule of (4n+2)π electrons.

A ring that contains six or ten π electrons acts as an aromatic ring.

The stability of a compound depends upon the number of resonating structures.

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Answer 5

Chapter 20.12, Problem 19P

Interpretation Introduction

Interpretation:

The resonance contributing structure of the thymine is to be drawn. The evidence that supports the statement that the thymine follows the Hückel’s rule is to be explained.

Concept introduction:

A molecule that is cyclic, planar, completely conjugated and follows Huckel’s rule is classified as an aromatic compound.

Aromatic compounds follow Huckel’s rule of (4n+2)π electrons.

A ring that contains six or ten π electrons acts as an aromatic ring.

The stability of a compound depends upon the number of resonating structures.

Answer 6

Chapter 20.12, Problem 19P

Interpretation Introduction

Interpretation:

The resonance contributing structure of the thymine is to be drawn. The evidence that supports the statement that the thymine follows the Hückel’s rule is to be explained.

Concept introduction:

A molecule that is cyclic, planar, completely conjugated and follows Huckel’s rule is classified as an aromatic compound.

Aromatic compounds follow Huckel’s rule of (4n+2)π electrons.

A ring that contains six or ten π electrons acts as an aromatic ring.

The stability of a compound depends upon the number of resonating structures.

Answer 7

Chapter 20.12, Problem 19P

Interpretation Introduction

Interpretation:

The resonance contributing structure of the thymine is to be drawn. The evidence that supports the statement that the thymine follows the Hückel’s rule is to be explained.

Concept introduction:

A molecule that is cyclic, planar, completely conjugated and follows Huckel’s rule is classified as an aromatic compound.

Aromatic compounds follow Huckel’s rule of (4n+2)π electrons.

A ring that contains six or ten π electrons acts as an aromatic ring.

The stability of a compound depends upon the number of resonating structures.

Answer 8

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Answer 9

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Answer 11

Ch. 20.1 - Prob. 1P Ch. 20.2 - Prob. 2P Ch. 20.3 - Prob. 3P Ch. 20.4 - Prob. 4P Ch. 20.5 - Prob. 5P Ch. 20.8 - Prob. 6P Ch. 20.8 - Prob. 7P Ch. 20.8 - Prob. 8P Ch. 20.9 - Prob. 9P Ch. 20.9 - Prob. 10P

Solution Summary: The author explains that the pyrimidine thymine follows Huckel's rule of (4n+2) electrons.

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