Organic Chemistry (Package) (Looseleaf)
Organic Chemistry (Package) (Looseleaf)
7th Edition
ISBN: 9780321939036
Author: Bruice
Publisher: PEARSON
Question
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Chapter 4.10, Problem 23P

(a)

Interpretation Introduction

Interpretation:

The observed specific reaction has to be calculated.

Concept introduction:

The pair of Enantiomers has different configurations.

Pair of enantiomers has different optical activity, which means if one will show levorotatory then the other will show dextrorotatory.

The direction and magnitude of rotation of plane-polarized light by an optically compound is measured by using polarimeter.

This rotation of polarized light is specific for a compound at specified temperature and wavelength, so it is called as Specific rotation of that compound.

The specific rotation of enantiomers has equal magnitudes and opposite signs.

Racemic mixture (equal amounts of enantiomers) of a compound has zero specific rotation.

(b)

Interpretation Introduction

Interpretation:

The observed specific reaction has to be calculated.

Concept introduction:

The pair of Enantiomers has different configurations.

Pair of enantiomers has different optical activity, which means if one will show levorotatory then the other will show dextrorotatory.

The direction and magnitude of rotation of plane-polarized light by an optically compound is measured by using polarimeter.

This rotation of polarized light is specific for a compound at specified temperature and wavelength, so it is called as Specific rotation of that compound.

The specific rotation of enantiomers has equal magnitudes and opposite signs.

Racemic mixture (equal amounts of enantiomers) of a compound has zero specific rotation.

If the mixture contain unequal amount of enantiomers of a compound, then the amount of excess of enantiomer is called enantiomeric excess or optical purity. It is calculated by,

enantiomericexcess=observedspecificrotationspecificrotationofthepureenantiomer×100%

(c)

Interpretation Introduction

Interpretation:

The observed specific reaction has to be calculated.

Concept introduction:

The pair of Enantiomers has different configurations.

Pair of enantiomers has different optical activity, which means if one will show levorotatory then the other will show dextrorotatory.

The direction and magnitude of rotation of plane-polarized light by an optically compound is measured by using polarimeter.

This rotation of polarized light is specific for a compound at specified temperature and wavelength, so it is called as Specific rotation of that compound.

The specific rotation of enantiomers has equal magnitudes and opposite signs.

Racemic mixture (equal amounts of enantiomers) of a compound has zero specific rotation.

If the mixture contain unequal amount of enantiomers of a compound, then the amount of excess of enantiomer is called enantiomeric excess or optical purity. It is calculated by,

enantiomericexcess=observedspecificrotationspecificrotationofthepureenantiomer×100%

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Chapter 4 Solutions

Organic Chemistry (Package) (Looseleaf)

Ch. 4.7 - Prob. 14PCh. 4.7 - Prob. 16PCh. 4.7 - Prob. 17PCh. 4.7 - Draw a perspective formula for each or the...Ch. 4.8 - Prob. 20PCh. 4.9 - Prob. 21PCh. 4.9 - (S)-(+)-Monosodium glutamate (MSG) is a flavor...Ch. 4.10 - Prob. 23PCh. 4.10 - Prob. 24PCh. 4.11 - Prob. 26PCh. 4.11 - Prob. 27PCh. 4.11 - Prob. 28PCh. 4.11 - The stereoisomer of cholesterol found in nature is...Ch. 4.11 - Prob. 30PCh. 4.12 - Prob. 31PCh. 4.12 - Draw all possible stereoisomers for each of the...Ch. 4.12 - Prob. 33PCh. 4.12 - Of all the possible cyclooctanes that have one...Ch. 4.12 - Prob. 35PCh. 4.12 - Prob. 36PCh. 4.13 - Which of the following compounds has a...Ch. 4.13 - Prob. 39PCh. 4.14 - Prob. 40PCh. 4.14 - Name the isomers you drew in Problem 52.Ch. 4.14 - Chloramphenicol is a broad-spectrum antibiotic...Ch. 4.14 - Draw a perspective formula for each of the...Ch. 4.14 - Name the following:Ch. 4.14 - Prob. 45PCh. 4.14 - Prob. 48PCh. 4.14 - Prob. 50PCh. 4.15 - Limonene exists as two different stereoisomers....Ch. 4.16 - Prob. 52PCh. 4 - a. Draw three constitutional isomers with...Ch. 4 - Prob. 53PCh. 4 - Prob. 54PCh. 4 - Which of the following has an asymmetric center?...Ch. 4 - Prob. 56PCh. 4 - Prob. 57PCh. 4 - Prob. 58PCh. 4 - Which of the following are optically active?Ch. 4 - Prob. 60PCh. 4 - Prob. 61PCh. 4 - Which of the following has an achiral...Ch. 4 - Prob. 63PCh. 4 - Prob. 64PCh. 4 - Prob. 65PCh. 4 - Prob. 66PCh. 4 - Prob. 67PCh. 4 - Prob. 68PCh. 4 - Prob. 69PCh. 4 - Prob. 70PCh. 4 - Prob. 71PCh. 4 - Prob. 72PCh. 4 - Prob. 73PCh. 4 - a. Draw all the isomers with molecular formula...Ch. 4 - Prob. 75PCh. 4 - Prob. 76PCh. 4 - Draw structures for the following: a....Ch. 4 - Prob. 78PCh. 4 - Prob. 79PCh. 4 - Prob. 80PCh. 4 - a. Using the wedge-and-dash notation, draw the...Ch. 4 - Prob. 82PCh. 4 - Prob. 83PCh. 4 - Prob. 84PCh. 4 - a. Draw the two chair conformers for each of the...Ch. 4 - Prob. 86PCh. 4 - Is the following compound optically active?
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