Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+)
Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+)
3rd Edition
ISBN: 9780137533268
Author: Paula Bruice
Publisher: PEARSON+
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Chapter 4.7, Problem 22P

(a)

Interpretation Introduction

Interpretation:

The representation of the given structure has to be identified as identical compounds or pair of enantiomers.

Concept introduction:

The pair of Enantiomers has different configurations.

Enantiomers are named by following Cahn-Ingold-Prelog system, in which R or S letter is used to differentiate between enantiomers.

According to Cahn-Ingold-Prelog system,

The group attached to asymmetric center should be ranked based on the atomic number of atom which directly connected to asymmetric center.  The higher the atomic number of atom, higher the priority.  If there is tie, then consider the next atoms attached to the connected atom and so on.

Check the direction of arrow drawn in the direction of decreasing priority.  If the arrow points clockwise direction, then the compound has R configuration.  If the arrow points counterclockwise direction, then the compound has S configuration.  If the group with lowest priority is not bonded by a hatched wedge, then interchange this group (lowest priority) by group bonded to hatched wedge and draw the arrow in priority order but the configuration is assigned as just reverse.

(b)

Interpretation Introduction

Interpretation:

The representation of the given structure has to be identified as identical compounds or pair of enantiomers.

Concept introduction:

The pair of Enantiomers has different configurations.

Enantiomers are named by following Cahn-Ingold-Prelog system, in which R or S letter is used to differentiate between enantiomers.

According to Cahn-Ingold-Prelog system,

The group attached to asymmetric center should be ranked based on the atomic number of atom which directly connected to asymmetric center.  The higher the atomic number of atom, higher the priority.  If there is tie, then consider the next atoms attached to the connected atom and so on.

Check the direction of arrow drawn in the direction of decreasing priority.  If the arrow points clockwise direction, then the compound has R configuration.  If the arrow points counterclockwise direction, then the compound has S configuration.  If the group with lowest priority is not bonded by a hatched wedge, then interchange this group (lowest priority) by group bonded to hatched wedge and draw the arrow in priority order but the configuration is assigned as just reverse.

(c)

Interpretation Introduction

Interpretation:

The representation of the given structure has to be identified as identical compounds or pair of enantiomers.

Concept introduction:

The pair of Enantiomers has different configurations.

Enantiomers are named by following Cahn-Ingold-Prelog system, in which R or S letter is used to differentiate between enantiomers.

According to Cahn-Ingold-Prelog system,

The group attached to asymmetric center should be ranked based on the atomic number of atom which directly connected to asymmetric center.  The higher the atomic number of atom, higher the priority.  If there is tie, then consider the next atoms attached to the connected atom and so on.

Check the direction of arrow drawn in the direction of decreasing priority.  If the arrow points clockwise direction, then the compound has R configuration.  If the arrow points counterclockwise direction, then the compound has S configuration.  If the group with lowest priority is not bonded by a hatched wedge, then interchange this group (lowest priority) by group bonded to hatched wedge and draw the arrow in priority order but the configuration is assigned as just reverse.

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Students have asked these similar questions
are these structures enantiomers, diastereomers, identical or other?
What is the relationship between the following pair of structures? H₂C H H CI CH3 They are diastereomers They are enantiomers They are identical H CH₂ H₂C The are constitutional isomers H
OH OH Br Br OH JOH OH OH OH ado Br Br OH all letters that apply all letters that apply all letters that apply A enantiomers B diasteromers C different conformations of the same molecule D identical comformations of the same molecule E constitutional isomers F stereoisomers G different molecules H both are chiral I neither is chiral

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Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+)

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