For the below compound, Fischer projection formula has to be drawn. Concept introduction: Fischer projections: In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.

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Answer 1

Question

Chapter 12, Problem 12.99AP

a.

Interpretation Introduction

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Fischer projections:

In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.

b.

Interpretation Introduction

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.

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When an unknown amine reacts with an unknown acid chloride, an amide with a molecular mass of 163 g/mol (M* = 163 m/z) is formed. In the infrared spectrum, important absorptions appear at 1661, 750 and 690 cm. The 13C NMR and DEPT spectra are provided. Draw the structure of the product as the resonance contributor lacking any formal charges. 13C NMR DEPT 90 200 160 120 80 40 0 200 160 120 80 40 0 DEPT 135 T 200 160 120 80 40 0 Draw the unknown amide. Select Dow Templates More Frage

Answer 2

Question

Chapter 12, Problem 12.99AP

a.

Interpretation Introduction

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Fischer projections:

In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.

b.

Interpretation Introduction

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.

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Answer 3

Question

Chapter 12, Problem 12.99AP

a.

Interpretation Introduction

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Fischer projections:

In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.

b.

Interpretation Introduction

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.

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Answer 4

Question

Chapter 12, Problem 12.99AP

a.

Interpretation Introduction

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Fischer projections:

In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.

b.

Interpretation Introduction

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.

Expert Solution & Answer

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Answer 5

Chapter 12, Problem 12.99AP

a.

Interpretation Introduction

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Fischer projections:

In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.

b.

Interpretation Introduction

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.

Answer 6

Chapter 12, Problem 12.99AP

a.

Interpretation Introduction

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Fischer projections:

In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.

Answer 7

Chapter 12, Problem 12.99AP

a.

Interpretation Introduction

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Fischer projections:

In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.

Answer 8

b.

Interpretation Introduction

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.

Answer 9

b.

Interpretation Introduction

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 12.1 - a. Label the hydroxyl groups, thiols, halogens,...Ch. 12.1 - Draw out each compound to clearly show what groups...Ch. 12.2 - Classify each alcohol as 1, 2, or 3.Ch. 12.2 - Classify each hydroxyl group in sorbitol as 1, 2,...Ch. 12.2 - Which compound in each pair has the higher boiling...Ch. 12.2 - Label each compound as water soluble or water...Ch. 12.2 - Give the IUPAC name for each compound.Ch. 12.2 - Give the structure corresponding to each name. a....Ch. 12.3 - Name each ether. a. CH3OCH2CH2CH2CH3 b....Ch. 12.3 - Prob. 12.10P

Solution Summary: The author explains that the chirality center of the organic compounds is drawn using the following convention.

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.

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Chapter 12 Solutions

Solution Summary: The author explains that the chirality center of the organic compounds is drawn using the following convention.

Interpretation: For the below compound, Fischer projection formula has to be drawn. Concept introduction: Refer to part ‘a.’.

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Chapter 12 Solutions

Interpretation:

For the below compound, Fischer projection formula has to be drawn.

Concept introduction:

Refer to part ‘a.’.