Using benzene and any other necessary amines how to synthesize sulfathiazole is to be shown. Concept introduction: The steps involved in the synthesis of sulfathiazole from benzene are i) Nitration of benzene ii) Reduction of nitrobenzene iii) Acetylation of the amino group iv) Chlorosulfonation of the anilide v) Treatment with 2-aminothiazole vi) Hydrolysis of the anilide to an amine. To Show: How to synthesize sulfathiazole starting from benzene and using any other necessary amines. Answer: The synthesis of sulfathiazole starting from benzene and using any other necessary amines is given below. Explanation: Nitration of benzene with Conc. HNO 3 and Conc. H 2 SO 4 yields nitrobenzene which on reduction with H 2 /Pt in ethanol gives aniline. Acetylation of aniline with acetic anhydride produces acetanilide. Chlorosulfonation of acetanilide leads to the formation of a p-chlorosulfonate as anilide group is orthp and para directing. Treatment of chlorosulfonate with 2-aminothiazole yields N-acetylsulfothiazole. Hydrolysis of N-acetylsulfothiazole yields sulfathiazole. Conclusion: The synthesis of sulfathiazole starting from benzene and using 2-aminothiazole is given below.

Question

None

Answer 1

Question

Chapter 24.8, Problem 16P

Interpretation Introduction

Interpretation:

Using benzene and any other necessary amines how to synthesize sulfathiazole is to be shown.

Concept introduction:

The steps involved in the synthesis of sulfathiazole from benzene are i) Nitration of benzene ii) Reduction of nitrobenzene iii) Acetylation of the amino group iv) Chlorosulfonation of the anilide v) Treatment with 2-aminothiazole vi) Hydrolysis of the anilide to an amine.

To Show:

How to synthesize sulfathiazole starting from benzene and using any other necessary amines.

Answer:

The synthesis of sulfathiazole starting from benzene and using any other necessary amines is given below.

Explanation:

Nitration of benzene with Conc. HNO₃ and Conc. H₂SO₄ yields nitrobenzene which on reduction with H₂/Pt in ethanol gives aniline. Acetylation of aniline with acetic anhydride produces acetanilide. Chlorosulfonation of acetanilide leads to the formation of a p-chlorosulfonate as anilide group is orthp and para directing. Treatment of chlorosulfonate with 2-aminothiazole yields N-acetylsulfothiazole. Hydrolysis of N-acetylsulfothiazole yields sulfathiazole.

Conclusion:

The synthesis of sulfathiazole starting from benzene and using 2-aminothiazole is given below.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

None

1. If the following molecule underwent a radical bromination (just add one bromine) - draw the product and then draw an energy diagram to explain why you drew the product you showed. Br₂ light ?

Please correct Answer and don't use Hand rating

Answer 2

Question

Chapter 24.8, Problem 16P

Interpretation Introduction

Interpretation:

Using benzene and any other necessary amines how to synthesize sulfathiazole is to be shown.

Concept introduction:

The steps involved in the synthesis of sulfathiazole from benzene are i) Nitration of benzene ii) Reduction of nitrobenzene iii) Acetylation of the amino group iv) Chlorosulfonation of the anilide v) Treatment with 2-aminothiazole vi) Hydrolysis of the anilide to an amine.

To Show:

How to synthesize sulfathiazole starting from benzene and using any other necessary amines.

Answer:

The synthesis of sulfathiazole starting from benzene and using any other necessary amines is given below.

Explanation:

Nitration of benzene with Conc. HNO₃ and Conc. H₂SO₄ yields nitrobenzene which on reduction with H₂/Pt in ethanol gives aniline. Acetylation of aniline with acetic anhydride produces acetanilide. Chlorosulfonation of acetanilide leads to the formation of a p-chlorosulfonate as anilide group is orthp and para directing. Treatment of chlorosulfonate with 2-aminothiazole yields N-acetylsulfothiazole. Hydrolysis of N-acetylsulfothiazole yields sulfathiazole.

Conclusion:

The synthesis of sulfathiazole starting from benzene and using 2-aminothiazole is given below.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 3

Question

Chapter 24.8, Problem 16P

Interpretation Introduction

Interpretation:

Using benzene and any other necessary amines how to synthesize sulfathiazole is to be shown.

Concept introduction:

The steps involved in the synthesis of sulfathiazole from benzene are i) Nitration of benzene ii) Reduction of nitrobenzene iii) Acetylation of the amino group iv) Chlorosulfonation of the anilide v) Treatment with 2-aminothiazole vi) Hydrolysis of the anilide to an amine.

To Show:

How to synthesize sulfathiazole starting from benzene and using any other necessary amines.

Answer:

The synthesis of sulfathiazole starting from benzene and using any other necessary amines is given below.

Explanation:

Nitration of benzene with Conc. HNO₃ and Conc. H₂SO₄ yields nitrobenzene which on reduction with H₂/Pt in ethanol gives aniline. Acetylation of aniline with acetic anhydride produces acetanilide. Chlorosulfonation of acetanilide leads to the formation of a p-chlorosulfonate as anilide group is orthp and para directing. Treatment of chlorosulfonate with 2-aminothiazole yields N-acetylsulfothiazole. Hydrolysis of N-acetylsulfothiazole yields sulfathiazole.

Conclusion:

The synthesis of sulfathiazole starting from benzene and using 2-aminothiazole is given below.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 4

Question

Chapter 24.8, Problem 16P

Interpretation Introduction

Interpretation:

Using benzene and any other necessary amines how to synthesize sulfathiazole is to be shown.

Concept introduction:

The steps involved in the synthesis of sulfathiazole from benzene are i) Nitration of benzene ii) Reduction of nitrobenzene iii) Acetylation of the amino group iv) Chlorosulfonation of the anilide v) Treatment with 2-aminothiazole vi) Hydrolysis of the anilide to an amine.

To Show:

How to synthesize sulfathiazole starting from benzene and using any other necessary amines.

Answer:

The synthesis of sulfathiazole starting from benzene and using any other necessary amines is given below.

Explanation:

Nitration of benzene with Conc. HNO₃ and Conc. H₂SO₄ yields nitrobenzene which on reduction with H₂/Pt in ethanol gives aniline. Acetylation of aniline with acetic anhydride produces acetanilide. Chlorosulfonation of acetanilide leads to the formation of a p-chlorosulfonate as anilide group is orthp and para directing. Treatment of chlorosulfonate with 2-aminothiazole yields N-acetylsulfothiazole. Hydrolysis of N-acetylsulfothiazole yields sulfathiazole.

Conclusion:

The synthesis of sulfathiazole starting from benzene and using 2-aminothiazole is given below.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 5

Chapter 24.8, Problem 16P

Interpretation Introduction

Interpretation:

Using benzene and any other necessary amines how to synthesize sulfathiazole is to be shown.

Concept introduction:

The steps involved in the synthesis of sulfathiazole from benzene are i) Nitration of benzene ii) Reduction of nitrobenzene iii) Acetylation of the amino group iv) Chlorosulfonation of the anilide v) Treatment with 2-aminothiazole vi) Hydrolysis of the anilide to an amine.

To Show:

How to synthesize sulfathiazole starting from benzene and using any other necessary amines.

Answer:

The synthesis of sulfathiazole starting from benzene and using any other necessary amines is given below.

Explanation:

Nitration of benzene with Conc. HNO₃ and Conc. H₂SO₄ yields nitrobenzene which on reduction with H₂/Pt in ethanol gives aniline. Acetylation of aniline with acetic anhydride produces acetanilide. Chlorosulfonation of acetanilide leads to the formation of a p-chlorosulfonate as anilide group is orthp and para directing. Treatment of chlorosulfonate with 2-aminothiazole yields N-acetylsulfothiazole. Hydrolysis of N-acetylsulfothiazole yields sulfathiazole.

Conclusion:

The synthesis of sulfathiazole starting from benzene and using 2-aminothiazole is given below.

Answer 6

Chapter 24.8, Problem 16P

Interpretation Introduction

Interpretation:

Using benzene and any other necessary amines how to synthesize sulfathiazole is to be shown.

Concept introduction:

The steps involved in the synthesis of sulfathiazole from benzene are i) Nitration of benzene ii) Reduction of nitrobenzene iii) Acetylation of the amino group iv) Chlorosulfonation of the anilide v) Treatment with 2-aminothiazole vi) Hydrolysis of the anilide to an amine.

To Show:

How to synthesize sulfathiazole starting from benzene and using any other necessary amines.

Answer:

The synthesis of sulfathiazole starting from benzene and using any other necessary amines is given below.

Explanation:

Nitration of benzene with Conc. HNO₃ and Conc. H₂SO₄ yields nitrobenzene which on reduction with H₂/Pt in ethanol gives aniline. Acetylation of aniline with acetic anhydride produces acetanilide. Chlorosulfonation of acetanilide leads to the formation of a p-chlorosulfonate as anilide group is orthp and para directing. Treatment of chlorosulfonate with 2-aminothiazole yields N-acetylsulfothiazole. Hydrolysis of N-acetylsulfothiazole yields sulfathiazole.

Conclusion:

The synthesis of sulfathiazole starting from benzene and using 2-aminothiazole is given below.

Answer 7

Chapter 24.8, Problem 16P

Interpretation Introduction

Interpretation:

Using benzene and any other necessary amines how to synthesize sulfathiazole is to be shown.

Concept introduction:

The steps involved in the synthesis of sulfathiazole from benzene are i) Nitration of benzene ii) Reduction of nitrobenzene iii) Acetylation of the amino group iv) Chlorosulfonation of the anilide v) Treatment with 2-aminothiazole vi) Hydrolysis of the anilide to an amine.

To Show:

How to synthesize sulfathiazole starting from benzene and using any other necessary amines.

Answer:

The synthesis of sulfathiazole starting from benzene and using any other necessary amines is given below.

Explanation:

Nitration of benzene with Conc. HNO₃ and Conc. H₂SO₄ yields nitrobenzene which on reduction with H₂/Pt in ethanol gives aniline. Acetylation of aniline with acetic anhydride produces acetanilide. Chlorosulfonation of acetanilide leads to the formation of a p-chlorosulfonate as anilide group is orthp and para directing. Treatment of chlorosulfonate with 2-aminothiazole yields N-acetylsulfothiazole. Hydrolysis of N-acetylsulfothiazole yields sulfathiazole.

Conclusion:

The synthesis of sulfathiazole starting from benzene and using 2-aminothiazole is given below.

Answer 8

Expert Solution & Answer

Answer 9

Expert Solution & Answer

Answer 10

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 11

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 12

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 13

Trending nowThis is a popular solution!

Answer 14

Trending nowThis is a popular solution!

Answer 15

Trending nowThis is a popular solution!

Answer 16

Trending now

Answer 17

This is a popular solution!

Answer 18

See solution

Check out sample textbook solution

Answer 19

Ch. 24.1 - Name the following compounds:Ch. 24.1 - Prob. 2P Ch. 24.1 - Prob. 3P Ch. 24.3 - Prob. 4P Ch. 24.3 - The benzylammonium ion (C6H5CH2NH3+) has pKa =...Ch. 24.4 - Prob. 6P Ch. 24.5 - Prob. 7P Ch. 24.6 - Prob. 8P Ch. 24.6 - Prob. 9P Ch. 24.6 - Show two methods for the synthesis of dopamine, a...

Solution Summary: The author describes the steps involved in the synthesis of sulfathiazole from benzene and using any other necessary amines.

Chapter 24 Solutions