The alkenes and the chemical reactions for the formation of these alkene when ( 2S,3S ) -3-bromo-2,3-diphenylpentane , ( 2S,3R ) -3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol are to be represented and the stereo specificity of the reactions is to be explained. Concept introduction: The elimination reaction is the organic reaction in which two substituents are removes from the organic molecule in one step or two steps. The two mechanism of the elimination reaction are E1 and E2 mechanism. In E2 mechanism, the elimination takes place in one step. The dehydrohalogenation reaction of the organic compound results in the formation of alkenes. They occur by the elimination of hydrogen halide. The stereo specificity is the property of the reaction that the formation of different stereo isomeric products formed from the different stereo isomeric reactants. To determine: The alkenes and the chemical reactions for the formation of these alkenes when ( 2S,3S ) -3-bromo-2,3-diphenylpentane , ( 2S,3R ) -3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol and the stereo specificity explanation of the reactions.

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Answer 1

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Chapter 7, Problem 7.66SP

Interpretation Introduction

Interpretation: The alkenes and the chemical reactions for the formation of these alkene when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol are to be represented and the stereo specificity of the reactions is to be explained.

Concept introduction: The elimination reaction is the organic reaction in which two substituents are removes from the organic molecule in one step or two steps. The two mechanism of the elimination reaction are E1 and E2 mechanism.

In E2 mechanism, the elimination takes place in one step.

The dehydrohalogenation reaction of the organic compound results in the formation of alkenes. They occur by the elimination of hydrogen halide.

The stereo specificity is the property of the reaction that the formation of different stereo isomeric products formed from the different stereo isomeric reactants.

To determine: The alkenes and the chemical reactions for the formation of these alkenes when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol and the stereo specificity explanation of the reactions.

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Answer 2

Question

Chapter 7, Problem 7.66SP

Interpretation Introduction

Interpretation: The alkenes and the chemical reactions for the formation of these alkene when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol are to be represented and the stereo specificity of the reactions is to be explained.

Concept introduction: The elimination reaction is the organic reaction in which two substituents are removes from the organic molecule in one step or two steps. The two mechanism of the elimination reaction are E1 and E2 mechanism.

In E2 mechanism, the elimination takes place in one step.

The dehydrohalogenation reaction of the organic compound results in the formation of alkenes. They occur by the elimination of hydrogen halide.

The stereo specificity is the property of the reaction that the formation of different stereo isomeric products formed from the different stereo isomeric reactants.

To determine: The alkenes and the chemical reactions for the formation of these alkenes when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol and the stereo specificity explanation of the reactions.

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Answer 3

Question

Chapter 7, Problem 7.66SP

Interpretation Introduction

Interpretation: The alkenes and the chemical reactions for the formation of these alkene when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol are to be represented and the stereo specificity of the reactions is to be explained.

Concept introduction: The elimination reaction is the organic reaction in which two substituents are removes from the organic molecule in one step or two steps. The two mechanism of the elimination reaction are E1 and E2 mechanism.

In E2 mechanism, the elimination takes place in one step.

The dehydrohalogenation reaction of the organic compound results in the formation of alkenes. They occur by the elimination of hydrogen halide.

The stereo specificity is the property of the reaction that the formation of different stereo isomeric products formed from the different stereo isomeric reactants.

To determine: The alkenes and the chemical reactions for the formation of these alkenes when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol and the stereo specificity explanation of the reactions.

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Answer 4

Question

Chapter 7, Problem 7.66SP

Interpretation Introduction

Interpretation: The alkenes and the chemical reactions for the formation of these alkene when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol are to be represented and the stereo specificity of the reactions is to be explained.

Concept introduction: The elimination reaction is the organic reaction in which two substituents are removes from the organic molecule in one step or two steps. The two mechanism of the elimination reaction are E1 and E2 mechanism.

In E2 mechanism, the elimination takes place in one step.

The dehydrohalogenation reaction of the organic compound results in the formation of alkenes. They occur by the elimination of hydrogen halide.

The stereo specificity is the property of the reaction that the formation of different stereo isomeric products formed from the different stereo isomeric reactants.

To determine: The alkenes and the chemical reactions for the formation of these alkenes when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol and the stereo specificity explanation of the reactions.

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Answer 5

Chapter 7, Problem 7.66SP

Interpretation Introduction

Interpretation: The alkenes and the chemical reactions for the formation of these alkene when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol are to be represented and the stereo specificity of the reactions is to be explained.

Concept introduction: The elimination reaction is the organic reaction in which two substituents are removes from the organic molecule in one step or two steps. The two mechanism of the elimination reaction are E1 and E2 mechanism.

In E2 mechanism, the elimination takes place in one step.

The dehydrohalogenation reaction of the organic compound results in the formation of alkenes. They occur by the elimination of hydrogen halide.

The stereo specificity is the property of the reaction that the formation of different stereo isomeric products formed from the different stereo isomeric reactants.

To determine: The alkenes and the chemical reactions for the formation of these alkenes when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol and the stereo specificity explanation of the reactions.

Answer 6

Chapter 7, Problem 7.66SP

Interpretation Introduction

Interpretation: The alkenes and the chemical reactions for the formation of these alkene when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol are to be represented and the stereo specificity of the reactions is to be explained.

Concept introduction: The elimination reaction is the organic reaction in which two substituents are removes from the organic molecule in one step or two steps. The two mechanism of the elimination reaction are E1 and E2 mechanism.

In E2 mechanism, the elimination takes place in one step.

The dehydrohalogenation reaction of the organic compound results in the formation of alkenes. They occur by the elimination of hydrogen halide.

The stereo specificity is the property of the reaction that the formation of different stereo isomeric products formed from the different stereo isomeric reactants.

To determine: The alkenes and the chemical reactions for the formation of these alkenes when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol and the stereo specificity explanation of the reactions.

Answer 7

Chapter 7, Problem 7.66SP

Interpretation Introduction

Interpretation: The alkenes and the chemical reactions for the formation of these alkene when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol are to be represented and the stereo specificity of the reactions is to be explained.

Concept introduction: The elimination reaction is the organic reaction in which two substituents are removes from the organic molecule in one step or two steps. The two mechanism of the elimination reaction are E1 and E2 mechanism.

In E2 mechanism, the elimination takes place in one step.

The dehydrohalogenation reaction of the organic compound results in the formation of alkenes. They occur by the elimination of hydrogen halide.

The stereo specificity is the property of the reaction that the formation of different stereo isomeric products formed from the different stereo isomeric reactants.

To determine: The alkenes and the chemical reactions for the formation of these alkenes when (2S,3S)-3-bromo-2,3-diphenylpentane, (2S,3R)-3-bromo-2,3-diphenylpentane reacts with solution of sodium ethoxide in ethanol and the stereo specificity explanation of the reactions.

Answer 8

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Answer 11

Ch. 7.3A - Prob. 7.1P Ch. 7.3A - Prob. 7.2P Ch. 7.3B - Draw five more compounds of formula C4H6NOC1.Ch. 7.3B - For each of the following molecular formulas,...Ch. 7.4 - Give the systematic (IUPAC) names of the following...Ch. 7.5B - The following names are all incorrect. Draw the...Ch. 7.5B - Prob. 7.8P Ch. 7.5B - a. How many stereogcmc double bonds are in...Ch. 7.6 - Teflon-coated frying pans routinely endure...Ch. 7.7B - Prob. 7.11P

Solution Summary: The author explains the elimination reaction, the dehydrohalogenation reaction and the stereo specificity of the reactions.

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