Mechanism should be drawn for all the given elimination reactions. Concept introduction: Mechanism: mechanism describes the reaction path and process. In reaction mechanism, curved arrows are used to show the electron transfer from one group to another. Curved arrow direction should be from lone pair electrons to electron deficient species such as carbocation etc. Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base. Elimination of compound in presence of bulky base leads to less substituted alkene , in presence of strong base (not bulky) leads to more substituted alkene.

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Answer 1

Question

Chapter 8.11, Problem 38CC

Interpretation Introduction

Interpretation:

Mechanism should be drawn for all the given elimination reactions.

Concept introduction:

Mechanism: mechanism describes the reaction path and process. In reaction mechanism, curved arrows are used to show the electron transfer from one group to another.

Curved arrow direction should be from lone pair electrons to electron deficient species such as carbocation etc.

Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base.

Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

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3. Name this ether correctly. H₁C H3C CH3 CH3 4. Show the best way to make the ether in #3 by a Williamson Ether Synthesis. Start from an alcohol or phenol. 5. Draw the structure of an example of a sulfide.

Answer 2

Question

Chapter 8.11, Problem 38CC

Interpretation Introduction

Interpretation:

Mechanism should be drawn for all the given elimination reactions.

Concept introduction:

Mechanism: mechanism describes the reaction path and process. In reaction mechanism, curved arrows are used to show the electron transfer from one group to another.

Curved arrow direction should be from lone pair electrons to electron deficient species such as carbocation etc.

Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base.

Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

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Answer 3

Question

Chapter 8.11, Problem 38CC

Interpretation Introduction

Interpretation:

Mechanism should be drawn for all the given elimination reactions.

Concept introduction:

Mechanism: mechanism describes the reaction path and process. In reaction mechanism, curved arrows are used to show the electron transfer from one group to another.

Curved arrow direction should be from lone pair electrons to electron deficient species such as carbocation etc.

Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base.

Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

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Answer 4

Question

Chapter 8.11, Problem 38CC

Interpretation Introduction

Interpretation:

Mechanism should be drawn for all the given elimination reactions.

Concept introduction:

Mechanism: mechanism describes the reaction path and process. In reaction mechanism, curved arrows are used to show the electron transfer from one group to another.

Curved arrow direction should be from lone pair electrons to electron deficient species such as carbocation etc.

Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base.

Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

Expert Solution & Answer

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Answer 5

Chapter 8.11, Problem 38CC

Interpretation Introduction

Interpretation:

Mechanism should be drawn for all the given elimination reactions.

Concept introduction:

Mechanism: mechanism describes the reaction path and process. In reaction mechanism, curved arrows are used to show the electron transfer from one group to another.

Curved arrow direction should be from lone pair electrons to electron deficient species such as carbocation etc.

Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base.

Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

Answer 6

Chapter 8.11, Problem 38CC

Interpretation Introduction

Interpretation:

Mechanism should be drawn for all the given elimination reactions.

Concept introduction:

Mechanism: mechanism describes the reaction path and process. In reaction mechanism, curved arrows are used to show the electron transfer from one group to another.

Curved arrow direction should be from lone pair electrons to electron deficient species such as carbocation etc.

Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base.

Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

Answer 7

Chapter 8.11, Problem 38CC

Interpretation Introduction

Interpretation:

Mechanism should be drawn for all the given elimination reactions.

Concept introduction:

Mechanism: mechanism describes the reaction path and process. In reaction mechanism, curved arrows are used to show the electron transfer from one group to another.

Curved arrow direction should be from lone pair electrons to electron deficient species such as carbocation etc.

Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base.

Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 8.3 - Prob. 1LTS Ch. 8.3 - Prob. 1PTS Ch. 8.3 - Prob. 2ATS Ch. 8.3 - Prob. 3ATS Ch. 8.3 - Prob. 4CC Ch. 8.4 - Prob. 2LTS Ch. 8.4 - Prob. 5PTS Ch. 8.4 - Prob. 6ATS Ch. 8.5 - Prob. 3LTS Ch. 8.5 - Prob. 7PTS

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