(a) Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated. Concept introduction: The strong nucleophiles that open epoxide ring are − OH, − OR , − CN, − SR, HC ≡ C − , and NH 3 . The reaction takes place through an S N 2 mechanism. The mechanism of overall reaction involves two steps.

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Answer 1

Question

Chapter 9.16, Problem 33P

Interpretation Introduction

(a)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Interpretation Introduction

(b)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

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a. Write the product For each of the Following reactions H 6-836-6 레 +H₂ N A H A-C-C=C-C-CH + 2 Na +2 NH3 - H H b. Write the reaction Mechanism For. reaction each

Answer 2

Question

Chapter 9.16, Problem 33P

Interpretation Introduction

(a)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Interpretation Introduction

(b)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

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Answer 3

Question

Chapter 9.16, Problem 33P

Interpretation Introduction

(a)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Interpretation Introduction

(b)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

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Answer 4

Question

Chapter 9.16, Problem 33P

Interpretation Introduction

(a)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Interpretation Introduction

(b)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

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Answer 5

Chapter 9.16, Problem 33P

Interpretation Introduction

(a)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Interpretation Introduction

(b)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Answer 6

Chapter 9.16, Problem 33P

Interpretation Introduction

(a)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Answer 7

Chapter 9.16, Problem 33P

Interpretation Introduction

(a)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Answer 8

Interpretation Introduction

(b)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Answer 9

Interpretation Introduction

(b)

Interpretation: The product of given reaction is to be drawn and the stereochemistry at any stereogenic center is to be indicated.

Concept introduction: The strong nucleophiles that open epoxide ring are −OH, −OR, −CN, −SR, HC≡C−, and NH3. The reaction takes place through an SN2 mechanism. The mechanism of overall reaction involves two steps.

Answer 10

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Answer 11

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Answer 13

Ch. 9.1 - Problem 9.1 Label each ether and alcohol in...Ch. 9.3 - Give the IUPAC name for each compound.Ch. 9.3 - Problem 9.3 Give the structure corresponding to...Ch. 9.3 - Name each of the following ethers.Ch. 9.3 - Name each epoxide. a. (two ways) b. c. (two...Ch. 9.6 - Problem 9.8 Draw the organic product of each...Ch. 9.6 - Prob. 9P Ch. 9.6 - Problem 9.10 Draw the products of each reaction. ...Ch. 9.8 - Problem 9.11 Draw the products formed when each...Ch. 9.8 - Prob. 12P

Solution Summary: The author explains that the product of given reaction is drawn and the stereochemistry at any stereogenic center is indicated.

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