Essential Organic Chemistry, Global Edition
Essential Organic Chemistry, Global Edition
3rd Edition
ISBN: 9781292089034
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 6, Problem 54P

(a)

Interpretation Introduction

Interpretation:

The rate of hydration of given alkenes should be determined.

Concept Introduction:

Stereoisomers: Two compounds with same molecular formula but different in their orientation are considered as isomers.

The presence of atom with non-super impossible mirror image is defined as enantiomers which are given R and S configuration based on the atoms bonded with them.

Erythro product: It is the representation of carbohydrates in Fischer projection when two same substituents are placed on the same side.

Threo product: It is the representation of carbohydrates in Fischer projection when two same substituents are placed on opposite side.

(b)

Interpretation Introduction

Interpretation:

The reason for the reactivity of (Z)-2-butene than (E)-2-butene should be determined.

Concept Introduction:

Stereoisomers: Two compounds with same molecular formula but different in their orientation are considered as isomers.

The presence of atom with non-super impossible mirror image is defined as enantiomers which are given R and S configuration based on the atoms bonded with them.

Erythro product: It is the representation of carbohydrates in Fischer projection when two same substituents are placed on the same side.

Threo product: It is the representation of carbohydrates in Fischer projection when two same substituents are placed on opposite side.

(c)

Interpretation Introduction

Interpretation:

The reason for the reactivity of 2-methyl-2-butene than (Z)-2-butene should be determined.

Concept Introduction:

Stereoisomers: Two compounds with same molecular formula but different in their orientation are considered as isomers.

The presence of atom with non-super impossible mirror image is defined as enantiomers which are given R and S configuration based on the atoms bonded with them.

Erythro product: It is the representation of carbohydrates in Fischer projection when two same substituents are placed on the same side.

Threo product: It is the representation of carbohydrates in Fischer projection when two same substituents are placed on opposite side.

(d)

Interpretation Introduction

Interpretation:

The reason for the reactivity of 2,3-dimethyl-2-butene than 2-methyl-2-butene should be determined.

Concept Introduction:

Stereoisomers: Two compounds with same molecular formula but different in their orientation are considered as isomers.

The presence of atom with non-super impossible mirror image is defined as enantiomers which are given R and S configuration based on the atoms bonded with them.

Erythro product: It is the representation of carbohydrates in Fischer projection when two same substituents are placed on the same side.

Threo product: It is the representation of carbohydrates in Fischer projection when two same substituents are placed on opposite side.

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Essential Organic Chemistry, Global Edition

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