Product and optical activity given following reaction has to be predicted. Concept Introduction: Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds . Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions. Benzene is an electron rich Aromatic compound . It undergoes aromatic electrophilic substitution reaction. The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance. Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule. Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another. Friedel - Crafts Alkylation : This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

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Answer 1

Question

Chapter 18, Problem 76IP

(a)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

(b)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

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Answer 2

Question

Chapter 18, Problem 76IP

(a)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

(b)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

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Answer 3

Question

Chapter 18, Problem 76IP

(a)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

(b)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

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Answer 4

Question

Chapter 18, Problem 76IP

(a)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

(b)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

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Answer 5

Chapter 18, Problem 76IP

(a)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

(b)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Answer 6

Chapter 18, Problem 76IP

(a)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Answer 7

Chapter 18, Problem 76IP

(a)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Answer 8

(b)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Answer 9

(b)

Interpretation Introduction

Interpretation:

Product and optical activity given following reaction has to be predicted.

Concept Introduction:

Electrophiles are electron deficient species. In Electrophilic substitution reaction a group or atom in a compound is replaced by electrophile. This kind of reaction occurs predominantly in aromatic compounds. Electrophilic substitution reactions of aromatic compounds are known as aromatic electrophilic substitution reactions.

Benzene is an electron rich Aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Enantiomers are chiral molecules to be mirror imagery of one another. In addition, the molecules are non-super imposable on one a new. This resource that the molecules cannot be placed on tops of one a further and give the similar molecule.

Diastereomers are stereoisomer’s that are not mirror images of one another and are non-super imposable on one another.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 18.2 - Prob. 1CC Ch. 18.3 - Prob. 2CC Ch. 18.3 - Prob. 3CC Ch. 18.4 - Prob. 4CC Ch. 18.5 - Prob. 5CC Ch. 18.5 - Prob. 6CC Ch. 18.5 - Prob. 7CC Ch. 18.6 - Prob. 8CC Ch. 18.6 - Prob. 9CC Ch. 18.6 - Prob. 10CC

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Chapter 18 Solutions