It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate. Concept Introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation. Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide . The alkylation is a S N 2 reaction. The alkylation works best with a primary alkyl halide. Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

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Answer 1

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Chapter 18.8, Problem 17P

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept Introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(b)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

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this is an inorganic chemistry question please answer accordindly!! its just one question with parts till (g) JUST ONE QUESTION with its parts spread out in the form of different images attached 2 IMAGES ATTACHED PLEASE SEE ALL, please answer EACH part till the end and dont just provide wordy explanations wherever asked for structures or diagrams, please DRAW DRAW them on a paper and post clearly!! answer the full question with all details EACH PART CLEARLY please thanks!! im reposting this please solve all parts and drawit not just word explanations!!

Answer 2

Question

Chapter 18.8, Problem 17P

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept Introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(b)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

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Answer 3

Question

Chapter 18.8, Problem 17P

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept Introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(b)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

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Answer 4

Question

Chapter 18.8, Problem 17P

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept Introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(b)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

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Answer 5

Chapter 18.8, Problem 17P

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept Introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(b)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

Answer 6

Chapter 18.8, Problem 17P

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept Introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

Answer 7

Chapter 18.8, Problem 17P

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept Introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

Answer 8

(b)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

Answer 9

(b)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

Answer 10

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

Answer 11

(a)

Interpretation Introduction

Interpretation: It should be described that how the given compound is prepared from cyclohexanone using an enamine intermediate.

Concept introduction: To increase the carbon chain, substituting an alkyl group on alpha carbon of a carbonyl group is called alkylation.

Alkylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate alkyl halide. The alkylation is a SN2 reaction. The alkylation works best with a primary alkyl halide.

Acylation is carried out by reaction of a ketone with a secondary amine in the presence of an acid to form an enamine and then adding an appropriate acyl halide. The acylation is an addition reaction.

Answer 12

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Ch. 18.1 - Prob. 1P Ch. 18.1 - Prob. 2P Ch. 18.1 - Prob. 3P Ch. 18.1 - Prob. 4P Ch. 18.1 - PROBLEM 5♦ List the compounds in each of the...Ch. 18.2 - Explain why 92% of 2,4-pemtanedione exists as the...Ch. 18.3 - Draw the enol tautomers for each of the following...Ch. 18.3 - Prob. 8P Ch. 18.4 - Prob. 9P Ch. 18.4 - Prob. 10P

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