To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant. Concept introduction: So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions. For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group. Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

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Answer 1

Question

Chapter 16, Problem 75P

a.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

b.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

c.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

d.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

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PLEASE ANSWER BOTH i) and ii) !!!!

E17E.2(a) The following mechanism has been proposed for the decomposition of ozone in the atmosphere: 03 → 0₂+0 k₁ O₁₂+0 → 03 K →> 2 k₁ Show that if the third step is rate limiting, then the rate law for the decomposition of O3 is second-order in O3 and of order −1 in O̟.

10.

Answer 2

Question

Chapter 16, Problem 75P

a.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

b.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

c.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

d.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

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Answer 3

Question

Chapter 16, Problem 75P

a.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

b.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

c.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

d.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

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Answer 4

Question

Chapter 16, Problem 75P

a.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

b.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

c.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

d.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

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Answer 5

Chapter 16, Problem 75P

a.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

b.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

c.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

d.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 6

Chapter 16, Problem 75P

a.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 7

Chapter 16, Problem 75P

a.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 8

b.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 9

b.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 10

c.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 11

c.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 12

d.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 13

d.

Interpretation Introduction

Interpretation:

To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.

For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.

Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

Answer 14

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Answer 15

Expert Solution & Answer

Answer 16

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Answer 17

Ch. 16.1 - Give two names for each of the following:Ch. 16.1 - Prob. 2P Ch. 16.1 - Name the following:Ch. 16.2 - Prob. 4P Ch. 16.4 - What products are formed when the following...Ch. 16.4 - We saw on the previous page that...Ch. 16.4 - a. How many stereoisomers are obtained from the...Ch. 16.4 - Prob. 9P Ch. 16.4 - Write the mechanism for the reaction of acetyl...Ch. 16.4 - Prob. 11P

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