(a) Interpretation: To predict the alkyl chloride needed to prepare A from B. Concept introduction: SN2 reaction is a special type of reaction mechanism in organic chemistry . It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp 3 hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

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Answer 1

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Chapter 7, Problem 7.79P

Interpretation Introduction

(a)

Interpretation:

To predict the alkyl chloride needed to prepare A from B.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Interpretation Introduction

(b)

Interpretation:

To predict the alkyl chloride is needed to prepare A from C.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

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What would be the best choices for the missing reagents 1 and 3 in this synthesis? 1. PPh3 3 2. n-BuLi • Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like. • Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is. • Note: if one of your reagents needs to contain a halogen, use bromine. Click and drag to start drawing a structure.

Answer 2

Question

Chapter 7, Problem 7.79P

Interpretation Introduction

(a)

Interpretation:

To predict the alkyl chloride needed to prepare A from B.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Interpretation Introduction

(b)

Interpretation:

To predict the alkyl chloride is needed to prepare A from C.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

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Answer 3

Question

Chapter 7, Problem 7.79P

Interpretation Introduction

(a)

Interpretation:

To predict the alkyl chloride needed to prepare A from B.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Interpretation Introduction

(b)

Interpretation:

To predict the alkyl chloride is needed to prepare A from C.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

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Answer 4

Question

Chapter 7, Problem 7.79P

Interpretation Introduction

(a)

Interpretation:

To predict the alkyl chloride needed to prepare A from B.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Interpretation Introduction

(b)

Interpretation:

To predict the alkyl chloride is needed to prepare A from C.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

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Answer 5

Chapter 7, Problem 7.79P

Interpretation Introduction

(a)

Interpretation:

To predict the alkyl chloride needed to prepare A from B.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Interpretation Introduction

(b)

Interpretation:

To predict the alkyl chloride is needed to prepare A from C.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Answer 6

Chapter 7, Problem 7.79P

Interpretation Introduction

(a)

Interpretation:

To predict the alkyl chloride needed to prepare A from B.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Answer 7

Chapter 7, Problem 7.79P

Interpretation Introduction

(a)

Interpretation:

To predict the alkyl chloride needed to prepare A from B.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Answer 8

Interpretation Introduction

(b)

Interpretation:

To predict the alkyl chloride is needed to prepare A from C.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Answer 9

Interpretation Introduction

(b)

Interpretation:

To predict the alkyl chloride is needed to prepare A from C.

Concept introduction:

SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp³ hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen.

Answer 10

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Answer 13

Ch. 7 - Classify each alkyl halide as 1 , 2, or 3.Ch. 7 - Problem 7.1 Telfairine, a naturally occurring...Ch. 7 - Draw the structure of an alkyl bromide with...Ch. 7 - Give the IUPAC name for each compound. a. b. c. d.Ch. 7 - Prob. 7.5P Ch. 7 - An sp3 hybridized CCl bond is more polar than an...Ch. 7 - Prob. 7.7P Ch. 7 - Problem 7.6 Identify the nucleophile and leaving...Ch. 7 - Prob. 7.9P Ch. 7 - Prob. 7.10P

Solution Summary: The author explains that SN2 reaction is a special type of reaction mechanism in organic chemistry.

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