“Diphenyl methane achieve co-planarity in the highest energy conformation” – it should be explained Concept introduction: For a compound that bears two aromatic rings separated by one carbon atom, the single bond experiences free rotation at room temperature Free rotation of the single bond enables the molecule to adopt different conformations When two rings are co-planar, there is a significant steric interaction between two of the aromatic hydrogen atoms. Steric interaction can be reduce by adopting a conformation in which the two rings are not coplanar

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Answer 1

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Chapter 18, Problem 45PP

Interpretation Introduction

Interpretation: “Diphenyl methane achieve co-planarity in the highest energy conformation” – it should be explained

Concept introduction:

For a compound that bears two aromatic rings separated by one carbon atom, the single bond experiences free rotation at room temperature

Free rotation of the single bond enables the molecule to adopt different conformations

When two rings are co-planar, there is a significant steric interaction between two of the aromatic hydrogen atoms.

Steric interaction can be reduce by adopting a conformation in which the two rings are not coplanar

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Answer 2

Question

Chapter 18, Problem 45PP

Interpretation Introduction

Interpretation: “Diphenyl methane achieve co-planarity in the highest energy conformation” – it should be explained

Concept introduction:

For a compound that bears two aromatic rings separated by one carbon atom, the single bond experiences free rotation at room temperature

Free rotation of the single bond enables the molecule to adopt different conformations

When two rings are co-planar, there is a significant steric interaction between two of the aromatic hydrogen atoms.

Steric interaction can be reduce by adopting a conformation in which the two rings are not coplanar

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 18, Problem 45PP

Interpretation Introduction

Interpretation: “Diphenyl methane achieve co-planarity in the highest energy conformation” – it should be explained

Concept introduction:

For a compound that bears two aromatic rings separated by one carbon atom, the single bond experiences free rotation at room temperature

Free rotation of the single bond enables the molecule to adopt different conformations

When two rings are co-planar, there is a significant steric interaction between two of the aromatic hydrogen atoms.

Steric interaction can be reduce by adopting a conformation in which the two rings are not coplanar

Expert Solution & Answer

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Check out a sample textbook solution

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Answer 4

Question

Chapter 18, Problem 45PP

Interpretation Introduction

Interpretation: “Diphenyl methane achieve co-planarity in the highest energy conformation” – it should be explained

Concept introduction:

For a compound that bears two aromatic rings separated by one carbon atom, the single bond experiences free rotation at room temperature

Free rotation of the single bond enables the molecule to adopt different conformations

When two rings are co-planar, there is a significant steric interaction between two of the aromatic hydrogen atoms.

Steric interaction can be reduce by adopting a conformation in which the two rings are not coplanar

Expert Solution & Answer

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Answer 5

Chapter 18, Problem 45PP

Interpretation Introduction

Interpretation: “Diphenyl methane achieve co-planarity in the highest energy conformation” – it should be explained

Concept introduction:

For a compound that bears two aromatic rings separated by one carbon atom, the single bond experiences free rotation at room temperature

Free rotation of the single bond enables the molecule to adopt different conformations

When two rings are co-planar, there is a significant steric interaction between two of the aromatic hydrogen atoms.

Steric interaction can be reduce by adopting a conformation in which the two rings are not coplanar

Answer 6

Chapter 18, Problem 45PP

Interpretation Introduction

Interpretation: “Diphenyl methane achieve co-planarity in the highest energy conformation” – it should be explained

Concept introduction:

For a compound that bears two aromatic rings separated by one carbon atom, the single bond experiences free rotation at room temperature

Free rotation of the single bond enables the molecule to adopt different conformations

When two rings are co-planar, there is a significant steric interaction between two of the aromatic hydrogen atoms.

Steric interaction can be reduce by adopting a conformation in which the two rings are not coplanar

Answer 7

Chapter 18, Problem 45PP

Interpretation Introduction

Interpretation: “Diphenyl methane achieve co-planarity in the highest energy conformation” – it should be explained

Concept introduction:

For a compound that bears two aromatic rings separated by one carbon atom, the single bond experiences free rotation at room temperature

Free rotation of the single bond enables the molecule to adopt different conformations

When two rings are co-planar, there is a significant steric interaction between two of the aromatic hydrogen atoms.

Steric interaction can be reduce by adopting a conformation in which the two rings are not coplanar

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 18.2 - Prob. 1LTS Ch. 18.2 - Prob. 1PTS Ch. 18.2 - Prob. 2ATS Ch. 18.2 - Prob. 3ATS Ch. 18.2 - Prob. 4ATS Ch. 18.2 - Prob. 5ATS Ch. 18.4 - Prob. 6CC Ch. 18.4 - Prob. 8CC Ch. 18.4 - Prob. 9CC Ch. 18.5 - Prob. 10CC

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Chapter 18 Solutions