Organic Chemistry: Structure and Function
Organic Chemistry: Structure and Function
8th Edition
ISBN: 9781319079451
Author: K. Peter C. Vollhardt, Neil E. Schore
Publisher: W. H. Freeman
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Chapter 5, Problem 37P

(a)

Interpretation Introduction

Interpretation:Each stereocenter in the indicated cyclohexane should be labeled as either R or S.

  Organic Chemistry: Structure and Function, Chapter 5, Problem 37P , additional homework tip  1

Concept introduction:In order to assign absolute configuration of R and S, Cahn − Ingold − Prelog rules are used and the first step is to assign the priority order on the basis of atomic number. The one with highest atomic number gest highest priority and is designated as a and so on.

The Fischer projection is written along with the priorities assigned and groups are interchanged between adjacent places so as to obtain lowest priority group at the bottom or lowest priority.

If the groups now are arranged are read from highest towards least in clockwise fashion the R is assigned to the stereocenter, if the rotation is anticlockwise the S is assigned at the configuration.

(b)

Interpretation Introduction

Interpretation:Each stereocenter in the indicated cyclohexane should be labeled as either R or S.

  Organic Chemistry: Structure and Function, Chapter 5, Problem 37P , additional homework tip  2

Concept introduction:In order to assign absolute configuration of R and S, Cahn − Ingold − Prelog rules are used and the first step is to assign the priority order on the basis of atomic number. The one with highest atomic number gest highest priority and is designated as a and so on.

The Fischer projection is written along with the priorities assigned and groups are interchanged between adjacent places so as to obtain lowest priority group at the bottom or lowest priority.

If the groups now are arranged are read from highest towards least in clockwise fashion the R is assigned to the stereocenter, if the rotation is anticlockwise the S is assigned at the configuration.

(c)

Interpretation Introduction

Interpretation:Each stereocenter in the indicated cyclohexane should be labeled as either R or S.

  Organic Chemistry: Structure and Function, Chapter 5, Problem 37P , additional homework tip  3

Concept introduction:In order to assign absolute configuration of R and S, Cahn − Ingold − Prelog rules are used and the first step is to assign the priority order on the basis of atomic number. The one with highest atomic number gest highest priority and is designated as a and so on.

The Fischer projection is written along with the priorities assigned and groups are interchanged between adjacent places so as to obtain lowest priority group at the bottom or lowest priority.

If the groups now are arranged are read from highest towards least in clockwise fashion the R is assigned to the stereocenter, if the rotation is anticlockwise the S is assigned at the configuration.

(d)

Interpretation Introduction

Interpretation:Each stereocenter in the indicated cyclohexane should be labeled as either R or S.

  Organic Chemistry: Structure and Function, Chapter 5, Problem 37P , additional homework tip  4

Concept introduction:In order to assign absolute configuration of R and S, Cahn − Ingold − Prelog rules are used and the first step is to assign the priority order on the basis of atomic number. The one with highest atomic number gest highest priority and is designated as a and so on.

The Fischer projection is written along with the priorities assigned and groups are interchanged between adjacent places so as to obtain lowest priority group at the bottom or lowest priority.

If the groups now are arranged are read from highest towards least in clockwise fashion the R is assigned to the stereocenter, if the rotation is anticlockwise the S is assigned at the configuration.

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Define each stereocenter as either (R) or (S). If the molecule does not have a stereocenter select "achiral". CH3 CI H CI CI CH3 H3C H3C., H 'CH3 Br H, Br Br Br
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