The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis. Concept Introduction : A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following Williamson ether synthesis in which sodium alkoxide and alkyl halide are used for bimolecular nucleophilic substitution reaction.

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Answer 1

Question

Chapter 7.11, Problem 36PTS

(a)

Interpretation Introduction

Interpretation:

The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following Williamson ether synthesis in which sodium alkoxide and alkyl halide are used for bimolecular nucleophilic substitution reaction.

(b)

Interpretation Introduction

Interpretation:

The transformation of the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for the synthesis of a target molecule. Williamson ether synthesis follows the SN2 pathway in which sodium alkoxide and alkyl halide are used.

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b) Certain cyclic compounds are known to be conformationally similar to carbohydrates, although they are not themselves carbohydrates. One example is Compound C shown below, which could be imagined as adopting four possible conformations. In reality, however, only one of these is particularly stable. Circle the conformation you expect to be the most stable, and provide an explanation to justify your choice. For your explanation to be both convincing and correct, it must contain not only words, but also "cartoon" orbital drawings contrasting the four structures. Compound C Possible conformations (circle one): Дет

Lab Data The distance entered is out of the expected range. Check your calculations and conversion factors. Verify your distance. Will the gas cloud be closer to the cotton ball with HCI or NH3? Did you report your data to the correct number of significant figures? - X Experimental Set-up HCI-NH3 NH3-HCI Longer Tube Time elapsed (min) 5 (exact) 5 (exact) Distance between cotton balls (cm) 24.30 24.40 Distance to cloud (cm) 9.70 14.16 Distance traveled by HCI (cm) 9.70 9.80 Distance traveled by NH3 (cm) 14.60 14.50 Diffusion rate of HCI (cm/hr) 116 118 Diffusion rate of NH3 (cm/hr) 175.2 175.2 How to measure distance and calculate rate

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Answer 2

Question

Chapter 7.11, Problem 36PTS

(a)

Interpretation Introduction

Interpretation:

The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following Williamson ether synthesis in which sodium alkoxide and alkyl halide are used for bimolecular nucleophilic substitution reaction.

(b)

Interpretation Introduction

Interpretation:

The transformation of the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for the synthesis of a target molecule. Williamson ether synthesis follows the SN2 pathway in which sodium alkoxide and alkyl halide are used.

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Answer 3

Question

Chapter 7.11, Problem 36PTS

(a)

Interpretation Introduction

Interpretation:

The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following Williamson ether synthesis in which sodium alkoxide and alkyl halide are used for bimolecular nucleophilic substitution reaction.

(b)

Interpretation Introduction

Interpretation:

The transformation of the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for the synthesis of a target molecule. Williamson ether synthesis follows the SN2 pathway in which sodium alkoxide and alkyl halide are used.

Expert Solution & Answer

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Answer 4

Question

Chapter 7.11, Problem 36PTS

(a)

Interpretation Introduction

Interpretation:

The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following Williamson ether synthesis in which sodium alkoxide and alkyl halide are used for bimolecular nucleophilic substitution reaction.

(b)

Interpretation Introduction

Interpretation:

The transformation of the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for the synthesis of a target molecule. Williamson ether synthesis follows the SN2 pathway in which sodium alkoxide and alkyl halide are used.

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Answer 5

Chapter 7.11, Problem 36PTS

(a)

Interpretation Introduction

Interpretation:

The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following Williamson ether synthesis in which sodium alkoxide and alkyl halide are used for bimolecular nucleophilic substitution reaction.

(b)

Interpretation Introduction

Interpretation:

The transformation of the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for the synthesis of a target molecule. Williamson ether synthesis follows the SN2 pathway in which sodium alkoxide and alkyl halide are used.

Answer 6

Chapter 7.11, Problem 36PTS

(a)

Interpretation Introduction

Interpretation:

The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following Williamson ether synthesis in which sodium alkoxide and alkyl halide are used for bimolecular nucleophilic substitution reaction.

Answer 7

Chapter 7.11, Problem 36PTS

(a)

Interpretation Introduction

Interpretation:

The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following Williamson ether synthesis in which sodium alkoxide and alkyl halide are used for bimolecular nucleophilic substitution reaction.

Answer 8

(b)

Interpretation Introduction

Interpretation:

The transformation of the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for the synthesis of a target molecule. Williamson ether synthesis follows the SN2 pathway in which sodium alkoxide and alkyl halide are used.

Answer 9

(b)

Interpretation Introduction

Interpretation:

The transformation of the target molecule must be shown along with Retrosynthetic analysis.

Concept Introduction :

A Retrosynthetic analysis helps to find out the suitable starting material for the synthesis of a target molecule. Williamson ether synthesis follows the SN2 pathway in which sodium alkoxide and alkyl halide are used.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 7.2 - Prob. 1CC Ch. 7.3 - Prob. 2CC Ch. 7.3 - Prob. 1LTS Ch. 7.3 - Prob. 3PTS Ch. 7.3 - Prob. 4ATS Ch. 7.3 - Prob. 2LTS Ch. 7.3 - Prob. 5PTS Ch. 7.3 - Prob. 6ATS Ch. 7.3 - Prob. 7CC Ch. 7.4 - Prob. 8CC

Solution Summary: The author explains that a retrosynthetic analysis helps to find out the suitable starting material for the synthesis of the target molecule.

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