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Practice Ch 22 Ans

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CHAPTER 22—REACTIONS OF BENZENE AND ITS DERIVATIVES MULTIPLE CHOICE 1. What is the major organic product obtained from the following reaction? a. 1 b. 2 c. 3 d. 4 ANS: B 2. What is the major organic product obtained from the following reaction? a. 1 b. 2 c. 3 d. 4 ANS: B 3. What is the major organic product obtained from the following reaction? 1
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Page 1: Practice Ch 22 Ans

CHAPTER 22—REACTIONS OF BENZENE AND ITS DERIVATIVES

MULTIPLE CHOICE

1. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: B

2. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: B

3. What is the major organic product obtained from the following reaction?

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Page 2: Practice Ch 22 Ans

a. 1b. 2c. 3d. 4

ANS: D

4. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: B

5. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: B

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Page 3: Practice Ch 22 Ans

6. What is the electrophile in the reaction of benzene with a mixture of nitric acid and sulfuric acid?a. HONOb. NO+

c. NO2+

d. benzene

ANS: B

7. What is the electrophile in the reaction of benzene with acetyl chloride, CH3COCl, and AlCl3?a. CH3CO+

b. CH3+

c. CH3CO2

d. benzene

ANS: A

8. What is the electrophile in the reaction of benzene with tert-butyl chloride and AlCl3?a. CH3

+

b. Cl+

c. (CH3)C+

d. benzene

ANS: C

9. What is the role of AlCl3 in Friedel Crafts acylations using acid chlorides?a. Lewis acidb. electrophilec. based. nucleophile

ANS: A

10. What is the role of FeBr3 in electrophilic aromatic bromination of benzene using Br2?a. nucleophileb. electrophilec. Lewis acidd. base

ANS: C

11. Which of the following undergoes the most rapid nitration upon treatment with HNO3/H2SO4?a. tolueneb. benzenec. bromobenzened. nitrobenzene

ANS: A

12. Which of the following undergoes the most rapid bromination upon treatment with Br2/FeBr3?a. benzeneb. nitrobenzenec. bromobenzened. anisole

ANS: D

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Page 4: Practice Ch 22 Ans

13. Which of the following undergoes the most rapid sulfonation upon treatment with fuming sulfuric acid?a. benzeneb. benzoic acidc. benzonitriled. nitrobenzene

ANS: A

14. Which of the following undergoes the most rapid acylation upon treatment with acetyl chloride and AlCl3?a. benzeneb. toluenec. chlorobenzened. 1,4-dichlorobenzene

ANS: B

15. Which of the following sets of substituents are all ortho/para directing in electrophilic aromatic substitution reactions?a. Cl, CH3, CNb. Br, OH, COCH3

c. Cl, OH, CH3

d. CN, NO2, COCH3

ANS: C

16. Which of the following sets of substituents are all ortho/para directing in electrophilic aromatic substitution reactions?a. Br, CH3, NO2

b. CH3, NH2, Brc. Cl, OCH3, COCH3

d. NO2, COCH3, COOH

ANS: B

17. Which of the following sets of substituents are all meta directing in electrophilic aromatic substitution reactions?a. CN, NO2, COCH3

b. CH3, OCH3, COCH3

c. Cl, NH2, CH3

d. CH3, NH3, OCH3

ANS: A

18. Which of the following sets of substituents are all meta directing in electrophilic aromatic substitution reactions?a. CH3, OH, Brb. Cl, NH2, CNc. COCH3, NO2, COOHd. NH2, COCH3, OH

ANS: C

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Page 5: Practice Ch 22 Ans

19. Which of the following sets of substituents are all activating groups in electrophilic aromatic substitution reactions?a. CH3, OCH3, COCH3

b. Cl, CN, NO2

c. Cl, NH2, CH3

d. CH3, NH2, OCH3

ANS: D

20. Which of the following sets of substituents are all activating groups in electrophilic aromatic substitution reactions?a. Br, NH2, CH3

b. CH3, NH2, OCH3

c. OH, COCH3, CH3,d. Br, CN, NO2

ANS: B

21. Which of the following sets of substituents are all deactivating groups in electrophilic aromatic substitution reactions?a. Cl, CN, NO2

b. Cl, NH2, CH3

c. CH3, OCH3, COCH3

d. CH3, NH2, OCH3

ANS: A

22. Which of the following sets of substituents are all deactivating groups in electrophilic aromatic substitution reactions?a. Cl, OH, CH2CH3

b. CH3, Br, COCH3

c. CH3, NH2, OHd. COCH3, NO2, Br

ANS: D

23. Which of the following substituents is ortho/para directing and deactivating in electrophilic aromatic substitution reactions?a. OHb. Clc. CH3

d. NO2

ANS: B

24. Which of the following substituents is ortho/para directing and deactivating in electrophilic aromatic substitution reactions?a. COCH3

b. NH3

c. Brd. CH2CH3

ANS: C

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Page 6: Practice Ch 22 Ans

25. Which of the following reactions or reaction sequences will not give isopropylbenzene as the major product?a. treatment of benzene with isopropyl alcohol and HFb. treatment of benzene with 1-chloropropane and AlCl3

c. treatment of benzene with propanoyl chloride and AlCl3; followed by reaction with Zn(Hg) and HCl

d. treatment of benzene with 1-propene and HF

ANS: C

26. Which of the following reactions or sequences will provide 1-propylbenzene as the major product?a. treatment of benzene with isopropyl alcohol and HFb. treatment of benzene with propanoyl chloride and AlCl3; followed by reaction with

Zn(Hg) and HClc. treatment of benzene with 1-chloropropane and AlCl3

d. treatment of benzene with 1-propene and HF

ANS: B

27. Which of the following are valid resonance structures of the electophile involved in Friedel-Crafts acylation of benzene upon treatment with CH3COCl and AlCl3?

a. 1b. 2c. 3d. 4

ANS: A

28. Which of the following is the structure of the complex of Br2 with FeBr3 involved in the electrophilic bromination of benzene?

a. 1b. 2c. 3d. 4

ANS: D

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Page 7: Practice Ch 22 Ans

29. Which of the following sets of reagents does not result in alkylation of benzene?a. tert-butyl chloride + AlCl3

b. tert-butyl alcohol + H3PO4

c. methylpropene + HFd. methylpropane + H2SO4

ANS: D

30. Why does nitrobenzene fail to undergo Fieldel-Crafts alkylation with tert-butyl chloride and AlCl3?a. nitrobenzene reacts with AlCl3

b. nitrobenzene is a poor nucleophilec. the nitro group is a strong electron donating groupd. the tert-butyl cation is a poor electrophile

ANS: B

31. Why does anisole undergo bromination with Br2 in the absence of FeBr3 whereas bromination of benzene requires the presence of FeBr3?a. anisole is a better nucleophile than benzeneb. the methoxy group of anisole is an inductive electron withdrawing substituentc. Br2 is a good nucleophiled. the reaction is accelerated by light

ANS: A

32. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: B

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Page 8: Practice Ch 22 Ans

33. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: C

34. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: A

35. What is the major organic product obtained from the following reaction?

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Page 9: Practice Ch 22 Ans

a. 1b. 2c. 3d. 4

ANS: B

36. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: B

37. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: D

9

Page 10: Practice Ch 22 Ans

38. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: D

39. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: D

10

Page 11: Practice Ch 22 Ans

40. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: B

41. What is the major organic product obtained from the following reaction?

a. 1b. 2c. 3d. 4

ANS: D

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Page 12: Practice Ch 22 Ans

42. What is the major organic product obtained from the following sequence of reactions?

a. 1b. 2c. 3d. 4

ANS: A

43. What is the major organic product obtained from the following sequence of reactions?

a. 1b. 2c. 3d. 4

ANS: C

12

Page 13: Practice Ch 22 Ans

44. What is the major organic product obtained from the following sequence of reactions?

a. 1b. 2c. 3d. 4

ANS: A

45. What is the major organic product obtained from the following sequence of reactions?

a. 1b. 2c. 3d. 4

ANS: C

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Page 14: Practice Ch 22 Ans

46. What is the major organic product obtained from the following sequence of reactions?

a. 1b. 2c. 3d. 4

ANS: D

47. What is the major organic product obtained from the following sequence of reactions?

a. 1b. 2c. 3d. 4

ANS: A

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Page 15: Practice Ch 22 Ans

48. Which of the following cannot be prepared from benzene in two synthetic steps?

a. 1b. 2c. 3d. 4

ANS: D

49. Which of the following cannot be prepared from benzene in two synthetic steps?

a. 1b. 2c. 3d. 4

ANS: A

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Page 16: Practice Ch 22 Ans

50. Which of the following is the reactive intermediate in the nucleophilic substitution of 4-bromo-1-nitrobenzene with sodium hydroxide?

a. 1b. 2c. 3d. 4

ANS: A

51. Which of the following is the reactive intermediate in the nucleophilic substitution of 4-bromo-1-toluene with sodium amide?

a. 1b. 2c. 3d. 4

ANS: D

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Page 17: Practice Ch 22 Ans

52. Which of the following is the reactive intermediate formed in the electrophilic bromination of toluene with Br2, FeBr3?

a. 1b. 2c. 3d. 4

ANS: C

53. Which of the following is the reactive intermediate formed in the electrophilic nitration of nitrobenzene with HNO3 and H2SO4?

a. 1b. 2c. 3d. 4

ANS: B

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Page 18: Practice Ch 22 Ans

54. Which of the following is the reactive intermediate formed in the electrophilic Friedel-Crafts acylation of toluene with CH3COCl and AlCl3?

a. 1b. 2c. 3d. 4

ANS: D

55. Which of the following compounds undergoes the most rapid nucleophilic substitution with hydroxide ion?

a. 1b. 2c. 3d. 4

ANS: D

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Page 19: Practice Ch 22 Ans

56. Which of the following compounds undergoes the most rapid nucleophilic substitution with hydroxide ion?

a. 1b. 2c. 3d. 4

ANS: C

57. Which of the following chlorobenzenes produces a single isomer upon treatment with NaNH2?

a. 1b. 2c. 3d. 4

ANS: D

58. Which of the following chlorobenzenes does not undergo nucleophilic aromatic substitution upon treatment with NaNH2?

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Page 20: Practice Ch 22 Ans

a. 1b. 2c. 3d. 4

ANS: A

59. Which mechanism accounts for the reaction of 4-bromo-1-nitrobenzene with sodium hydroxide to form 4-nitrophenol?a. Bimolecular nucleophilic substitution (SN2)b. Nucleophilic aromatic substitution by elimination-additionc. Nucleophilic aromatic substitution by addition-eliminationd. Electrophilic aromatic substitution

ANS: C

60. Which mechanism accounts for the reaction of chlorobenzene with acetyl chloride and AlCl3 to form 4-chloroacetophenone?a. Bimolecular nucleophilic substitution (SN2)b. Nucleophilic aromatic substitution by elimination-additionc. Nucleophilic aromatic substitution by addition-eliminationd. Electrophilic aromatic substitution

ANS: D

61. Which mechanism accounts for the reaction of benzyl chloride with sodium cyanide to form cyanomethylbenzene (phenylacetonitrile, PhCH2CN)?a. Bimolecular nucleophilic substitution (SN2)b. Nucleophilic aromatic substitution by elimination-additionc. Nucleophilic aromatic substitution by addition-eliminationd. Electrophilic aromatic substitution

ANS: A

62. Which mechanism accounts for the reaction of 4-bromotoluene with sodium amide to form a mixture of 3- and 4-aminotoluene?a. Bimolecular nucleophilic substitution (SN2)b. Nucleophilic aromatic substitution by elimination-additionc. Nucleophilic aromatic substitution by addition-eliminationd. Electrophilic aromatic substitution

ANS: B

63. What type of intermediate is formed in the reaction between chlorobenzene and tert-butyl chloride and AlCl3 to give 4-chloro-1-tert-butylbenzene?a. Meisenheimer complexb. benzynec. cyclohexadienyl cationd. benzyl radical

ANS: C

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Page 21: Practice Ch 22 Ans

64. What type of intermediate is formed in the reaction between bromobenzene and sodium amide to give aniline?a. Meisenheimer complexb. benzynec. cyclohexadienyl cationd. benzyl radical

ANS: B

65. What type of intermediate is formed in upon irradiation of a mixture of toluene and chlorine to give benzyl chloride?a. Meisenheimer complexb. benzynec. cyclohexadienyl cationd. benzyl radical

ANS: D

68. Which of the following is not true about benzynes?a. They are planarb. They are formed upon dehydrohalogenation of aryl halidesc. They are aromaticd. They are intermediates in nucleophilic aromatic substitution reaction which take place by

an addition-elimination mechanism

ANS: D

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Page 22: Practice Ch 22 Ans

69. Predict the product of the following reaction:

A)

B)

C)

D)

E) none of these

ANS: A

22

E

E

E

E

E

Page 23: Practice Ch 22 Ans

70 What major product would you expect from the following reaction?

A)

B)

C)

D)

E)

A

ANS: A

23

OH

? HNO3 H2SO4

OH

NO2

OH

O2N

NO2OH

OH

NO2

OH

NO2

Page 24: Practice Ch 22 Ans

71. Predict the major organic product of the following reaction.

A)

B)

C)

D)

E)

24

O

CH3O

NO2

NO2

Br2 / FeBr3?

O

CH3O

NO2

NO2

Br

O

CH3O

NO2

NO2

Br

O

CH3O

NO2

NO2

Br

CH3O

NO2

NO2

OHBr

Page 25: Practice Ch 22 Ans

ANS: A

PROBLEM

1. What is the major organic product obtained from the following reaction?

ANS:

2. What is the major organic product obtained from the following reaction?

ANS:

25

O

CH3O

NO2

NO2

Br

Page 26: Practice Ch 22 Ans

3. What is the major organic product obtained from the following reaction?

ANS:

4. What is the major organic product obtained from the following reaction?

ANS:

5. What is the major organic product obtained from the following reaction?

26

Page 27: Practice Ch 22 Ans

ANS:

27

Page 28: Practice Ch 22 Ans

6. What is the major organic product obtained from the following reaction?

ANS:

7. What is the major organic product obtained from the following sequence of reactions (if a reaction is

likely to give you a mixture of ortho and para disubstituted compounds you should assume that they can be separated; continue the synthesis with either one)?

ANS:

8. What is the major organic product obtained from the following reaction (if a reaction is likely to give

you a mixture of ortho and para disubstituted compounds you should assume that they can be separated; continue the synthesis with either one)?

28

Page 29: Practice Ch 22 Ans

29

Page 30: Practice Ch 22 Ans

ANS:

9. What is the major organic product obtained from the following sequence of reactions (if a reaction is likely to give you a mixture of ortho and para disubstituted compounds you should assume that they can be separated; continue the synthesis with either one)?

ANS:

10. What is the major organic product obtained from the following reaction (assume that mixtures of ortho

and para disubstituted compounds can be separated; continue the synthesis with either one)?

ANS:

or ortho isomer

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Page 31: Practice Ch 22 Ans

11. What is the major organic product obtained from the following reaction (assume that mixtures of ortho and para disubstituted compounds can be separated; continue the synthesis with either one)?

ANS:

12. Provide the structure (a single resonance contributor) of the key intermediate in the electrophilic

aromatic nitration of chlorobenzene.

ANS:

13. Provide the structure (a single resonance contributor) of the key intermediate in the electrophilic

aromatic chlorinatio of nitroobenzene.

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Page 32: Practice Ch 22 Ans

ANS:

14. Provide the structure (a single resonance contributor) of the key intermediate in the following reaction.

ANS:

15. Provide the structure (a single resonance contributor) of the key intermediate in the following reaction.

ANS:

16) Provide a series of synthetic steps by which 2-bromo-4-nitrobenzoic acid can be prepared

32

Page 33: Practice Ch 22 Ans

from toluene.Answer: 1. HNO3, H2SO42. Br2, FeBr33. KMnO4, OH-, Δ4. H+Diff: 3

17) Provide a series of synthetic steps by which 3-bromoethylbenzene can be prepared from benzene.Answer: 1. CH3COCl, AlCl32. Br2, FeBr33. Zn(Hg), HClDiff: 3

18) Provide a series of synthetic steps by which 4-t-butylbenzoic acid can be prepared from toluene.Answer: 1. (CH3)3CCl, AlCl32. KMnO4, OH-, Δ3. H+Diff: 3

19) Provide a series of synthetic steps by which p-nitrobutylbenzene can be prepared from benzene.Answer: 1. CH3CH2CH2COCl, AlCl32. Zn(Hg), HCl3. HNO3, H2SO4Diff: 3

20) Provide a series of synthetic steps by which 4-phenylheptan-4-ol can be prepared from benzene.Answer: 1. Br2, FeBr32. Mg, ether3. CH3CH2CH2COCH2CH2CH34. H3O+

Diff: 3

33


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