(a) Interpretation: The products formed by the treatment of benzoic anhydride [ ( C 6 H 5 CO ) 2 O ] with H 2 O are to be drawn. Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

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Answer 1

Question

Chapter 20.8, Problem 13P

Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

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Answer 2

Question

Chapter 20.8, Problem 13P

Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

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Answer 3

Question

Chapter 20.8, Problem 13P

Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

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Answer 4

Question

Chapter 20.8, Problem 13P

Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

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Answer 5

Chapter 20.8, Problem 13P

Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 6

Chapter 20.8, Problem 13P

Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 7

Chapter 20.8, Problem 13P

Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 8

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 9

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 10

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 11

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 12

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 13

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Answer 14

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Answer 15

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Answer 16

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Answer 17

Ch. 20.1 - Prob. 1P Ch. 20.2 - Draw the three possible resonance structures for...Ch. 20.2 - Prob. 3P Ch. 20.3 - Give an IUPAC or common name for each compound. a....Ch. 20.3 - Problem 22.5 Draw the structure corresponding to...Ch. 20.4 - Problem 22.6 Explain why the boiling point of is...Ch. 20.7 - Prob. 11P Ch. 20.7 - Prob. 12P Ch. 20.8 - Prob. 13P Ch. 20.9 - Problem 22.16 Draw the products of each reaction. ...

Solution Summary: The author explains that the products formed by the treatment of benzoic anhydride are drawn.

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