The enantiomers of Plavix are to be drawn and the enantiomer of Plavix with the S configuration is to be identified. Concept introduction: The stereochemistry of the compound is determined by prioritizing the groups attached to its stereogenic center. The groups are prioritized on the basis of atomic number of their atoms. The group that contain atom with higher atomic number is given higher priority. Complete the circle in decreasing order of priority from 1 → 2 → 3 . The configuration of the compound is R and S when circle rotates in clockwise and anticlockwise direction.

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Answer 1

Question

Chapter 5.6, Problem 17P

Interpretation Introduction

Interpretation: The enantiomers of Plavix are to be drawn and the enantiomer of Plavix with the S configuration is to be identified.

Concept introduction: The stereochemistry of the compound is determined by prioritizing the groups attached to its stereogenic center. The groups are prioritized on the basis of atomic number of their atoms. The group that contain atom with higher atomic number is given higher priority. Complete the circle in decreasing order of priority from 1→2→3. The configuration of the compound is R and S when circle rotates in clockwise and anticlockwise direction.

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Answer 2

Question

Chapter 5.6, Problem 17P

Interpretation Introduction

Interpretation: The enantiomers of Plavix are to be drawn and the enantiomer of Plavix with the S configuration is to be identified.

Concept introduction: The stereochemistry of the compound is determined by prioritizing the groups attached to its stereogenic center. The groups are prioritized on the basis of atomic number of their atoms. The group that contain atom with higher atomic number is given higher priority. Complete the circle in decreasing order of priority from 1→2→3. The configuration of the compound is R and S when circle rotates in clockwise and anticlockwise direction.

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Answer 3

Question

Chapter 5.6, Problem 17P

Interpretation Introduction

Interpretation: The enantiomers of Plavix are to be drawn and the enantiomer of Plavix with the S configuration is to be identified.

Concept introduction: The stereochemistry of the compound is determined by prioritizing the groups attached to its stereogenic center. The groups are prioritized on the basis of atomic number of their atoms. The group that contain atom with higher atomic number is given higher priority. Complete the circle in decreasing order of priority from 1→2→3. The configuration of the compound is R and S when circle rotates in clockwise and anticlockwise direction.

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Answer 4

Question

Chapter 5.6, Problem 17P

Interpretation Introduction

Interpretation: The enantiomers of Plavix are to be drawn and the enantiomer of Plavix with the S configuration is to be identified.

Concept introduction: The stereochemistry of the compound is determined by prioritizing the groups attached to its stereogenic center. The groups are prioritized on the basis of atomic number of their atoms. The group that contain atom with higher atomic number is given higher priority. Complete the circle in decreasing order of priority from 1→2→3. The configuration of the compound is R and S when circle rotates in clockwise and anticlockwise direction.

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Answer 5

Chapter 5.6, Problem 17P

Interpretation Introduction

Interpretation: The enantiomers of Plavix are to be drawn and the enantiomer of Plavix with the S configuration is to be identified.

Concept introduction: The stereochemistry of the compound is determined by prioritizing the groups attached to its stereogenic center. The groups are prioritized on the basis of atomic number of their atoms. The group that contain atom with higher atomic number is given higher priority. Complete the circle in decreasing order of priority from 1→2→3. The configuration of the compound is R and S when circle rotates in clockwise and anticlockwise direction.

Answer 6

Chapter 5.6, Problem 17P

Interpretation Introduction

Interpretation: The enantiomers of Plavix are to be drawn and the enantiomer of Plavix with the S configuration is to be identified.

Concept introduction: The stereochemistry of the compound is determined by prioritizing the groups attached to its stereogenic center. The groups are prioritized on the basis of atomic number of their atoms. The group that contain atom with higher atomic number is given higher priority. Complete the circle in decreasing order of priority from 1→2→3. The configuration of the compound is R and S when circle rotates in clockwise and anticlockwise direction.

Answer 7

Chapter 5.6, Problem 17P

Interpretation Introduction

Interpretation: The enantiomers of Plavix are to be drawn and the enantiomer of Plavix with the S configuration is to be identified.

Concept introduction: The stereochemistry of the compound is determined by prioritizing the groups attached to its stereogenic center. The groups are prioritized on the basis of atomic number of their atoms. The group that contain atom with higher atomic number is given higher priority. Complete the circle in decreasing order of priority from 1→2→3. The configuration of the compound is R and S when circle rotates in clockwise and anticlockwise direction.

Answer 8

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Answer 11

Ch. 5.1 - Prob. 1P Ch. 5.2 - Prob. 2P Ch. 5.3 - Draw the mirror image of each compound. Label each...Ch. 5.3 - Prob. 4P Ch. 5.3 - A molecule is achiral if it has a plane of...Ch. 5.6 - Prob. 17P Ch. 5.6 - Prob. 18P Ch. 5.7 - Prob. 19P Ch. 5.7 - Prob. 20P Ch. 5.7 - Problem 5.18 Compounds E and F are two isomers of...

Solution Summary: The author explains the stereochemistry of Plavix by prioritizing the groups attached to its stereogenic center. The chiral center of clopidogrel is shown in Figure 1.

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