The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds. Concept introduction: Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”. When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other. The Trans isomers have high symmetry and are more stable than cis isomers.

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Answer 1

Question

Chapter 4, Problem 4.70AP

a.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

b.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

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Answer 2

Question

Chapter 4, Problem 4.70AP

a.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

b.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

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Answer 3

Question

Chapter 4, Problem 4.70AP

a.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

b.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

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Answer 4

Question

Chapter 4, Problem 4.70AP

a.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

b.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

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Answer 5

Chapter 4, Problem 4.70AP

a.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

b.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

Answer 6

Chapter 4, Problem 4.70AP

a.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

Answer 7

Chapter 4, Problem 4.70AP

a.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

Answer 8

b.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

Answer 9

b.

Summary Introduction

To determine:

The structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

Concept introduction:

Cis-trans isomers come under the geometric isomerism and are a form of stereoisomerism. The prefix “cis” means “on the same side” and the prefix “trans” means “on opposite sides”.

When the heteroatom is cis then one heteroatom is at axial position and the other one is at equatorial position. When the heteroatom is trans, then both substituents are at equatorial position but are on the opposite sides of the ring with respect to each other.

The Trans isomers have high symmetry and are more stable than cis isomers.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 4 - Prob. 4.1PP Ch. 4 - Prob. 4.2PP Ch. 4 - Prob. 4.3PP Ch. 4 - Draw a skeletal structure for ethane, C2H6. Do you...Ch. 4 - Prob. 4.5PP Ch. 4 - Prob. 4.6PP Ch. 4 - Draw a Lewis structure for each of the following...Ch. 4 - Draw a Lewis structure for each of the following...Ch. 4 - Prob. 4.9PP Ch. 4 - Prob. 4.10PP

Solution Summary: The author explains the structure of both the cis and trans stereoisomers for the given compound using wedge-and-dash bonds.

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