The product obtained in skraup synthesis by replacing aniline with para-ethylaniline has to be given. Concept Introduction: Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Question

Want to see the full answer?

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 19, Problem 38P

(a)

Interpretation Introduction

Interpretation:

The product obtained in skraup synthesis by replacing aniline with para-ethylaniline has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(b)

Interpretation Introduction

Interpretation: The product obtained in skraup synthesis by replacing glycerol with 3-hexen-2-one has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(c)

Interpretation Introduction

Interpretation: The reactants required for the preparation of 2,7-diethyl-3-methylquinoline in skraup synthesis should be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Speaking of composite materials, indicate the correct option:(A). Composite materials can only be: metal-polymer or polymer-polymer.(B). Composite materials can be made up of particles, but not fibers or sheets.(C). When the reinforcing particles are uniformly distributed in a composite material, there may be a greater tendency for it to have isotropic properties.(D). None of the above is correct.

If we are talking about viscoelastic modulus or viscoelastic relaxation modulus in polymers, indicate the correct option.(A). It reports the variation of elastic behavior as a function of time.(B). It is only useful for defining its glass transition temperature.(C). It only allows us to define the polymer degradation temperature.(D). Neither option is correct.

When natural light falls perpendicularly on a material A, it has a reflectivity of 0.813%. Indicate the value of the refractive index.

Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 19, Problem 38P

(a)

Interpretation Introduction

Interpretation:

The product obtained in skraup synthesis by replacing aniline with para-ethylaniline has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(b)

Interpretation Introduction

Interpretation: The product obtained in skraup synthesis by replacing glycerol with 3-hexen-2-one has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(c)

Interpretation Introduction

Interpretation: The reactants required for the preparation of 2,7-diethyl-3-methylquinoline in skraup synthesis should be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 19, Problem 38P

(a)

Interpretation Introduction

Interpretation:

The product obtained in skraup synthesis by replacing aniline with para-ethylaniline has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(b)

Interpretation Introduction

Interpretation: The product obtained in skraup synthesis by replacing glycerol with 3-hexen-2-one has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(c)

Interpretation Introduction

Interpretation: The reactants required for the preparation of 2,7-diethyl-3-methylquinoline in skraup synthesis should be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 19, Problem 38P

(a)

Interpretation Introduction

Interpretation:

The product obtained in skraup synthesis by replacing aniline with para-ethylaniline has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(b)

Interpretation Introduction

Interpretation: The product obtained in skraup synthesis by replacing glycerol with 3-hexen-2-one has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(c)

Interpretation Introduction

Interpretation: The reactants required for the preparation of 2,7-diethyl-3-methylquinoline in skraup synthesis should be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 19, Problem 38P

(a)

Interpretation Introduction

Interpretation:

The product obtained in skraup synthesis by replacing aniline with para-ethylaniline has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(b)

Interpretation Introduction

Interpretation: The product obtained in skraup synthesis by replacing glycerol with 3-hexen-2-one has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

(c)

Interpretation Introduction

Interpretation: The reactants required for the preparation of 2,7-diethyl-3-methylquinoline in skraup synthesis should be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Answer 6

Chapter 19, Problem 38P

(a)

Interpretation Introduction

Interpretation:

The product obtained in skraup synthesis by replacing aniline with para-ethylaniline has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Answer 7

Chapter 19, Problem 38P

(a)

Interpretation Introduction

Interpretation:

The product obtained in skraup synthesis by replacing aniline with para-ethylaniline has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Answer 8

(b)

Interpretation Introduction

Interpretation: The product obtained in skraup synthesis by replacing glycerol with 3-hexen-2-one has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Answer 9

(b)

Interpretation Introduction

Interpretation: The product obtained in skraup synthesis by replacing glycerol with 3-hexen-2-one has to be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Answer 10

(c)

Interpretation Introduction

Interpretation: The reactants required for the preparation of 2,7-diethyl-3-methylquinoline in skraup synthesis should be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Answer 11

(c)

Interpretation Introduction

Interpretation: The reactants required for the preparation of 2,7-diethyl-3-methylquinoline in skraup synthesis should be given.

Concept Introduction:

Skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in the formation of cyclic ring which on reduction gives quinoline.

Answer 12

Expert Solution & Answer

Answer 13

Expert Solution & Answer

Answer 14

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 15

Ch. 19.1 - Name the following:Ch. 19.2 - Prob. 3P Ch. 19.2 - Prob. 4P Ch. 19.3 - Draw the product of each of the following...Ch. 19.5 - Prob. 6P Ch. 19.5 - Explain why cyclopentadiene (pKa = 15) is more...Ch. 19.5 - When pyrrole is added to a dilute solution of...Ch. 19.6 - Prob. 10P Ch. 19.6 - How to the mechanisms of the following reactions...Ch. 19.6 - Prob. 12P

Solution Summary: The author explains that skraup synthesis is the reaction of aniline with an alpha-beta unsaturated carbonyl compound and proceeds through the formation of carbocation and results in cyclic ring

Concept explainers

Want to see the full answer?

Chapter 19 Solutions