a) Interpretation: Fischer projections of the following molecules are to be given. The S enantiomer of 2-bromobutane. Concept introduction: In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page. For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned. To show: Fischer projections of the following molecules. The S enantiomer of 2-bromobutane.

Question

Consider the following gas chromatographs of Compound A, Compound B, and a mixture of Compounds A and B. Inject A B mixture Area= 9 Area = 5 Area = 3 Area Inject . མི། Inject J2 What is the percentage of Compound B in the the mixture?

Answer 1

Question

Chapter 25.SE, Problem 42AP

Interpretation Introduction

a)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 2-bromobutane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The S enantiomer of 2-bromobutane.

Interpretation Introduction

b)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of alanine.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of alanine.

Interpretation Introduction

c)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of 2-hydroxypropionic acid.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of 2-hydroxypropionic acid.

Interpretation Introduction

d)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 3-methylhexane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.
For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.
To show:

The S enantiomer of 3-methylhexane.

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Consider the following gas chromatographs of Compound A, Compound B, and a mixture of Compounds A and B. Inject A B mixture Area= 9 Area = 5 Area = 3 Area Inject . མི། Inject J2 What is the percentage of Compound B in the the mixture?

Rank these according to stability. CH3 H3C CH3 1 CH3 H3C 1 most stable, 3 least stable O 1 most stable, 2 least stable 2 most stable, 1 least stable O2 most stable, 3 least stable O3 most stable, 2 least stable O3 most stable, 1 least stable CH3 2 CH3 CH3 H₂C CH3 3 CH3 CH

Consider this IR and NMR: INFRARED SPECTRUM TRANSMITTANCE 0.8- 0.6 0.4 0.2 3000 10 9 8 00 HSP-00-541 7 CO 6 2000 Wavenumber (cm-1) сл 5 ppm 4 M Which compound gave rise to these spectra? N 1000 1 0

Answer 2

Question

Chapter 25.SE, Problem 42AP

Interpretation Introduction

a)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 2-bromobutane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The S enantiomer of 2-bromobutane.

Interpretation Introduction

b)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of alanine.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of alanine.

Interpretation Introduction

c)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of 2-hydroxypropionic acid.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of 2-hydroxypropionic acid.

Interpretation Introduction

d)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 3-methylhexane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.
For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.
To show:

The S enantiomer of 3-methylhexane.

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Answer 3

Question

Chapter 25.SE, Problem 42AP

Interpretation Introduction

a)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 2-bromobutane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The S enantiomer of 2-bromobutane.

Interpretation Introduction

b)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of alanine.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of alanine.

Interpretation Introduction

c)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of 2-hydroxypropionic acid.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of 2-hydroxypropionic acid.

Interpretation Introduction

d)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 3-methylhexane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.
For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.
To show:

The S enantiomer of 3-methylhexane.

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Answer 4

Question

Chapter 25.SE, Problem 42AP

Interpretation Introduction

a)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 2-bromobutane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The S enantiomer of 2-bromobutane.

Interpretation Introduction

b)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of alanine.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of alanine.

Interpretation Introduction

c)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of 2-hydroxypropionic acid.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of 2-hydroxypropionic acid.

Interpretation Introduction

d)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 3-methylhexane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.
For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.
To show:

The S enantiomer of 3-methylhexane.

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Answer 5

Chapter 25.SE, Problem 42AP

Interpretation Introduction

a)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 2-bromobutane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The S enantiomer of 2-bromobutane.

Interpretation Introduction

b)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of alanine.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of alanine.

Interpretation Introduction

c)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of 2-hydroxypropionic acid.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of 2-hydroxypropionic acid.

Interpretation Introduction

d)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 3-methylhexane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.
For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.
To show:

The S enantiomer of 3-methylhexane.

Answer 6

Chapter 25.SE, Problem 42AP

Interpretation Introduction

a)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 2-bromobutane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The S enantiomer of 2-bromobutane.

Answer 7

Chapter 25.SE, Problem 42AP

Interpretation Introduction

a)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 2-bromobutane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The S enantiomer of 2-bromobutane.

Answer 8

Interpretation Introduction

b)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of alanine.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of alanine.

Answer 9

Interpretation Introduction

b)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of alanine.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of alanine.

Answer 10

Interpretation Introduction

c)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of 2-hydroxypropionic acid.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of 2-hydroxypropionic acid.

Answer 11

Interpretation Introduction

c)

Interpretation:

Fischer projections of the following molecules are to be given.

The R enantiomer of 2-hydroxypropionic acid.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.

For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.

To show:

Fischer projections of the following molecules.

The R enantiomer of 2-hydroxypropionic acid.

Answer 12

Interpretation Introduction

d)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 3-methylhexane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.
For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.
To show:

The S enantiomer of 3-methylhexane.

Answer 13

Interpretation Introduction

d)

Interpretation:

Fischer projections of the following molecules are to be given.

The S enantiomer of 3-methylhexane.

Concept introduction:

In Fischer projection formula, a tetrahedral carbon is represented by two crossed lines. The horizontal line represents bonds coming out of the page and vertical lines represent bonds moving in to the page.
For assigning R or S configuration, the four groups attached to the chiral center are arranged in the order of priority by applying sequence rules. The molecule is then oriented in such a way that the group of lowest priority points away from the viewer. If the arrangement of highest priority to second highest priority to third highest priority is clockwise then R configuration is assigned. If the arrangement of highest priority to second highest priority to third highest priority is counterclockwise then S configuration is assigned.
To show:

The S enantiomer of 3-methylhexane.

Answer 14

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Ch. 25.1 - Prob. 1P Ch. 25.2 - Prob. 2P Ch. 25.2 - Prob. 3P Ch. 25.2 - Prob. 4P Ch. 25.2 - Prob. 5P Ch. 25.3 - Prob. 6P Ch. 25.3 - Prob. 7P Ch. 25.4 - Prob. 8P Ch. 25.4 - Prob. 9P Ch. 25.4 - Prob. 10P

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Chapter 25 Solutions