ORGANIC CHEMISTRY (LL)-PACKAGE
ORGANIC CHEMISTRY (LL)-PACKAGE
8th Edition
ISBN: 9781319316389
Author: VOLLHARDT
Publisher: MAC HIGHER
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Chapter 2, Problem 41P

(a)

Interpretation Introduction

Interpretation: Curved arrows to depict electron movement for the reaction between bromoethane and OH should be shown

Concept introduction: The fundamental electrostatics suggests that electrons have more affinity for electron deficient sites in an organic compound. or positive charge. The curved arrow is appropriate mechanism to depict electron movement that occurs from electron rich species to electron deficient species.

The nucleophile is species with unshared lone pair or negative charge that makes it seek out positive center with a reaction. Likewise, electrophile seeks for electron rich center as it is positively charged center of substrate.

(b)

Interpretation Introduction

Interpretation: Curved arrows to depict electron movement for the reaction between propanal and nitrogen of ammonia should be shown.

Concept introduction: The fundamental electrostatics suggests that electrons have more affinity for electron deficient sites in an organic compound. or positive charge. The curved arrow is appropriate mechanism to depict electron movement that occurs from electron rich species to electron deficient species.

The nucleophile is species with unshared lone pair or negative charge that makes it seek out positive center with a reaction. Likewise, electrophile seeks for electron rich center as it is positively charged center of substrate.

(c)

Interpretation Introduction

Interpretation: Curved arrows to depict electron movement for the reaction between Methoxyethane and should be shown.

Concept introduction: The fundamental electrostatics suggests that electrons have more affinity for electron deficient sites in an organic compound. or positive charge. The curved arrow is appropriate mechanism to depict electron movement that occurs from electron rich species to electron deficient species.

The nucleophile is species with unshared lone pair or negative charge that makes it seek out positive center with a reaction. Likewise, electrophile seeks for electron rich center as it is positively charged center of substrate.

(d)

Interpretation Introduction

Interpretation: Curved arrows to depict electron movement for the reaction of 3-hexanone and should be shown.

Concept introduction: The fundamental electrostatics suggests that electrons have more affinity for electron deficient sites in an organic compound. or positive charge. The curved arrow is appropriate mechanism to depict electron movement that occurs from electron rich species to electron deficient species.

The nucleophile is species with unshared lone pair or negative charge that makes it seek out positive center with a reaction. Likewise, electrophile seeks for electron rich center as it is positively charged center of substrate.

(e)

Interpretation Introduction

Interpretation: Curved arrows to depict electron movement for the reaction of acetonitrile and CH3+ be shown.

Concept introduction: The fundamental electrostatics suggests that electrons have more affinity for electron deficient sites in an organic compound. or positive charge. The curved arrow is appropriate mechanism to depict electron movement that occurs from electron rich species to electron deficient species.

The nucleophile is species with unshared lone pair or negative charge that makes it seek out positive center with a reaction. Likewise, electrophile seeks for electron rich center as it is positively charged center of substrate.

(f)

Interpretation Introduction

Interpretation: Curved arrows to depict electron movement for the reaction of butane and OH be shown.

Concept introduction: The fundamental electrostatics suggests that electrons have more affinity for electron deficient sites in an organic compound. or positive charge. The curved arrow is appropriate mechanism to depict electron movement that occurs from electron rich species to electron deficient species.

The nucleophile is species with unshared lone pair or negative charge that makes it seek out positive center with a reaction. Likewise, electrophile seeks for electron rich center as it is positively charged center of substrate.

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