ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
2nd Edition
ISBN: 9780393664034
Author: KARTY
Publisher: NORTON
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Chapter 5, Problem 5.53P
Interpretation Introduction

(a)

Interpretation:

Whether the compounds in the given pair have the same or different boiling points is to be determined.

Concept introduction:

Isomers are the pair of compounds that have the same formula.

Constitutional isomers are the isomers having the same molecular formula but different connectivity. Constitutional isomers must have different physical and chemical properties.

The configurational isomers are not interconvertible by rotating around a single bond.

Enantiomers are configurational isomers having the same connectivity but cannot be interconvertible by rotation around a single bond. The mirror images of enantiomers are non-superimposable. Since enantiomers have the same connectivity of atoms, they should behave identically.

Diastereomers are configurational isomers having same connectivity but are not mirror images of each other. Diastereomers show different physical and chemical properties. Cis-trans isomers are diastereomers.

The boiling point of isomers comes under physical property.

Expert Solution
Check Mark

Answer to Problem 5.53P

The given pair of isomers have different boiling points as they are diastereomers of each other.

Explanation of Solution

The given pair of compounds is

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5, Chapter 5, Problem 5.53P , additional homework tip  1 ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5, Chapter 5, Problem 5.53P , additional homework tip  2

Both the molecules in the given pair have the same molecular formula; they also have the same connectivity. Thus, they are configurational isomers. The given pair of molecules is cis-trans isomers. So, these compounds are diastereomers of each other. Diastereomers show different physical and chemical properties. Thus, the compounds in the given pair should have different boiling points.

Conclusion

The given pair of isomers have different boiling point as they are diastereomers of each other.

Interpretation Introduction

(b)

Interpretation:

Whether the compounds in the given pair have the same or different boiling points is to be determined.

Concept introduction:

Isomers are the pair of compounds that have the same formula.

Constitutional isomers are the isomers having the same molecular formula but different connectivity. Constitutional isomers must have different physical and chemical properties.

The configurational isomers are not interconvertible by rotating around a single bond.

Enantiomers are configurational isomers having the same connectivity but cannot be interconvertible by rotation around a single bond. The mirror images of enantiomers are non-superimposable. Since enantiomers have the same connectivity of atoms, they should behave identically.

Diastereomers are configurational isomers that have the same connectivity but are not mirror images of each other. Diastereomers have different physical and chemical properties. Cis-trans isomers are diastereomers of each other.

The boiling point of isomers comes under physical property.

Expert Solution
Check Mark

Answer to Problem 5.53P

The given pair of isomers have different boiling points as they are constitutional isomers of each other.

Explanation of Solution

The given pair of compounds is

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5, Chapter 5, Problem 5.53P , additional homework tip  3

Both the molecules in the given pair have the same molecular formula, so they are isomers.

However, they do not have same connectivity of atoms. In both the compounds, there are two OH groups attached on the cyclohexane.

In the first compound, the OH groups are attached on C1 and C3 carbon atoms. In the second compound, the OH groups are attached on C1 and C4 carbon atoms. This indicates that both the isomers do not have the same connectivity of atoms. Thus, the given pair of compounds are constitutional isomers of each other. Constitutional isomers have different physical and chemical properties. Thus, the compounds in the given pair should have different boiling points.

Conclusion

The given pair of isomers have different boiling points as they are constitutional isomers of each other.

Interpretation Introduction

(c)

Interpretation:

Whether the compounds in the given pair have the same or different boiling points is to be determined.

Concept introduction:

Isomers are the pair of compounds that have the same formula.

Constitutional isomers are the isomers having the same molecular formula but different connectivity. Constitutional isomers must have different physical and chemical properties.

The configurational isomers are not interconvertible by rotating around a single bond.

Enantiomers are configurational isomers having the same connectivity but cannot be interconvertible by rotation around a single bond. The mirror images of enantiomers are non-superimposable. Since enantiomers have the same connectivity of atoms, they should behave identically.

Diastereomers are configurational isomers that have the same connectivity but are not mirror images of each other. Diastereomers have different physical and chemical properties. Cis-trans isomers are diastereomers of each other.

The boiling point of isomers comes under physical property.

In a Fischer projection, exchanging two groups on an asymmetric carbon atoms gives the opposite stereochemical configuration.

Expert Solution
Check Mark

Answer to Problem 5.53P

The given pair of isomers should have different boiling points as they are diastereomers of each other.

Explanation of Solution

The given pair of compounds is

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5, Chapter 5, Problem 5.53P , additional homework tip  4

Both the molecules in the given pair have the same molecular formula. They also have the same connectivity. Thus, they are configurational isomers.

Each molecule has three chiral centers at C2, C3, and C4 carbon atoms. Note that in the second compound, the two groups on C3 chiral carbon have been exchanged. This suggests that the stereochemical configurations at C3 carbon atoms in both the compounds are opposite to each other. Remaining stereo centers have the same stereochemical configuration, suggesting that the two compounds are diastereomers of each other. Diastereomers have different physical and chemical properties. Thus, the compounds in the given pair should have different boiling points.

Conclusion

The given pair of isomers have different boiling points as they are diastereomers of each other.

Interpretation Introduction

(d)

Interpretation:

Whether the compounds in the given pair have the same or different boiling points is to be determined.

Concept introduction:

Isomers are the pair of compounds that have the same formula.

Constitutional isomers are the isomers having the same molecular formula but different connectivity. Constitutional isomers must have different physical and chemical properties.

The configurational isomers are not interconvertible by rotating around a single bond.

Enantiomers are configurational isomers having the same connectivity but cannot be interconvertible by rotation around a single bond. The mirror images of enantiomers are non-superimposable. Since enantiomers have the same connectivity of atoms, they should behave identically.

Diastereomers are configurational isomers that have the same connectivity but are not mirror images of each other. Diastereomers have different physical and chemical properties. Cis-trans isomers are diastereomers of each other. Cyclic alkanes exhibit cis-trans isomerism.

The boiling point of isomers comes under physical property.

Expert Solution
Check Mark

Answer to Problem 5.53P

The given pair of isomers should have different boiling points as they are diastereomers of each other.

Explanation of Solution

The given pair of compounds is

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5, Chapter 5, Problem 5.53P , additional homework tip  5

In both the compounds, the OH groups are attached on C1 and C3 carbon atoms. In the first molecule, the two OH groups are on the same side of the ring and hence are cis to each other. In the second molecule, the two OH groups are on the opposite side of the ring and hence are trans to each other. Cis-trans isomers are diastereomers of each other. Diastereomers have different physical and chemical properties. Thus, the compounds in the given pair should have different boiling points.

Conclusion

The given pair of isomers have different boiling points as they are diastereomers of each other.

Interpretation Introduction

(e)

Interpretation:

Whether the compounds in the given pair have the same or different boiling points is to be determined.

Concept introduction:

Isomers are the pair of compounds that have the same formula.

Constitutional isomers are the isomers having the same molecular formula but different connectivity. Constitutional isomers must have different physical and chemical properties.

The configurational isomers are not interconvertible by rotating around a single bond.

Enantiomers are configurational isomers having the same connectivity but cannot be interconvertible by rotation around a single bond. The mirror images of enantiomers are non-superimposable. Since enantiomers have the same connectivity of atoms, they should behave identically.

The boiling point of isomers comes under physical property.

Expert Solution
Check Mark

Answer to Problem 5.53P

The given pair of isomers should have the same boiling point as they are enantiomers of each other.

Explanation of Solution

The given pair of compounds is

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5, Chapter 5, Problem 5.53P , additional homework tip  6

In both the compounds, the OH group is attached on the same carbon atom. In both the compounds, the carbon atom having the OH group attached is the chiral center.

The stereochemical configuration at the chiral center in the first molecule is S as the top-three priority groups are arranged in a counterclockwise manner, and the fourth-priority group is on a dash bond.

The stereochemical configuration at the chiral center in the second molecule is R as the top-three priority groups are arranged in a counterclockwise manner, but the fourth-priority group is on a wedge bond.

Thus, the stereochemical configuration at the chiral centers for two molecules is opposite. This indicates that the two compounds must be enantiomers of each other. Enantiomers have precisely the same physical and chemical properties. Hence the two compounds in the given pair have the same boiling points.

Conclusion

The given pair of isomers should have the same boiling point as they are enantiomers of each other.

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Chapter 5 Solutions

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5

Ch. 5 - Prob. 5.11PCh. 5 - Prob. 5.12PCh. 5 - Prob. 5.13PCh. 5 - Prob. 5.14PCh. 5 - Prob. 5.15PCh. 5 - Prob. 5.16PCh. 5 - Prob. 5.17PCh. 5 - Prob. 5.18PCh. 5 - Prob. 5.19PCh. 5 - Prob. 5.20PCh. 5 - Prob. 5.21PCh. 5 - Prob. 5.22PCh. 5 - Prob. 5.23PCh. 5 - Prob. 5.24PCh. 5 - Prob. 5.25PCh. 5 - Prob. 5.26PCh. 5 - Prob. 5.27PCh. 5 - Prob. 5.28PCh. 5 - Prob. 5.29PCh. 5 - Prob. 5.30PCh. 5 - Prob. 5.31PCh. 5 - Prob. 5.32PCh. 5 - Prob. 5.33PCh. 5 - Prob. 5.34PCh. 5 - Prob. 5.35PCh. 5 - Prob. 5.36PCh. 5 - Prob. 5.37PCh. 5 - Prob. 5.38PCh. 5 - Prob. 5.39PCh. 5 - Prob. 5.40PCh. 5 - Prob. 5.41PCh. 5 - Prob. 5.42PCh. 5 - Prob. 5.43PCh. 5 - Prob. 5.44PCh. 5 - Prob. 5.45PCh. 5 - Prob. 5.46PCh. 5 - Prob. 5.47PCh. 5 - Prob. 5.48PCh. 5 - Prob. 5.49PCh. 5 - Prob. 5.50PCh. 5 - Prob. 5.51PCh. 5 - Prob. 5.52PCh. 5 - Prob. 5.53PCh. 5 - Prob. 5.54PCh. 5 - Prob. 5.55PCh. 5 - Prob. 5.56PCh. 5 - Prob. 5.57PCh. 5 - Prob. 5.58PCh. 5 - Prob. 5.59PCh. 5 - Prob. 5.60PCh. 5 - Prob. 5.61PCh. 5 - Prob. 5.62PCh. 5 - Prob. 5.63PCh. 5 - Prob. 5.64PCh. 5 - Prob. 5.65PCh. 5 - Prob. 5.66PCh. 5 - Prob. 5.67PCh. 5 - Prob. 5.68PCh. 5 - Prob. 5.69PCh. 5 - Prob. 5.70PCh. 5 - Prob. 5.71PCh. 5 - Prob. 5.72PCh. 5 - Prob. 5.73PCh. 5 - Prob. 5.74PCh. 5 - Prob. 5.75PCh. 5 - Prob. 5.76PCh. 5 - Prob. 5.77PCh. 5 - Prob. 5.78PCh. 5 - Prob. 5.79PCh. 5 - Prob. 5.1YTCh. 5 - Prob. 5.2YTCh. 5 - Prob. 5.3YTCh. 5 - Prob. 5.4YTCh. 5 - Prob. 5.5YTCh. 5 - Prob. 5.6YTCh. 5 - Prob. 5.7YTCh. 5 - Prob. 5.8YTCh. 5 - Prob. 5.9YTCh. 5 - Prob. 5.10YTCh. 5 - Prob. 5.11YTCh. 5 - Prob. 5.12YTCh. 5 - Prob. 5.13YTCh. 5 - Prob. 5.14YTCh. 5 - Prob. 5.15YTCh. 5 - Prob. 5.16YTCh. 5 - Prob. 5.17YT
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