Organic Chemistry
Organic Chemistry
3rd Edition
ISBN: 9781119338352
Author: Klein
Publisher: WILEY
Question
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Chapter 19.3, Problem 5CC

a)

Interpretation Introduction

Interpretation:

To determine the necessary reagent to achieve the following transformation.

Concept Introduction:

Reagent: it is a substance or compound added to a chemical reaction and which donates a chemical ingredient (a compound of mixture, typically of organic or inorganic substance.

Examples include the Collins reagent, Fenton’s reagent and the most popular Grignard’s reagent etc…

Ozonolysis: it’s an organic reaction where the unsaturated bonds alkanes and alkynes compounds are broken with ozone.

Alkenes and alkynes form organic compound, which have multiple carbon-carbon bond and it has been replaced by a carbonyl group.

Oxidizing reagent: it’s composed of oxidant and oxidizer. It has a tendency to oxidized the other substance.

It’s formed when a molecule or ions loose its electron.

Common oxidizing agents are oxygen, hydrogen peroxide, and halogens.

Redox reaction: redox reaction is that type of reaction where both oxidation and reduction takes place.

This is the popular Aromatic electrophilic substitution reaction and are classified into two types

1-Friedel Craft Alkylation:-It involves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid catalyst with anhydrous Ferrichloride as a catalyst and thhe alkyl group attached at the former site of the chloride ion.

2-Fridel Craft Acylation: - It involves the acylation of aromatic rings with an acyl chloride using a strong Lewis acid catalyst. Like AlCl3 catalyst.

b)

Interpretation Introduction

Interpretation:

To determine the necessary reagent to achieve the following transformation.

Concept Introduction:

Reagent: it is a substance or compound added to a chemical reaction and which donates a chemical ingredient (a compound of mixture, typically of organic or inorganic substance.

Examples include the Collins reagent, Fenton’s reagent and the most popular Grignard’s reagent etc…

Ozonolysis: it’s an organic reaction where the unsaturated bonds alkanes and alkynes compounds are broken with ozone.

Alkenes and alkynes form organic compound, which have multiple carbon-carbon bond and it has been replaced by a carbonyl group.

Oxidizing reagent: it’s composed of oxidant and oxidizer. It has a tendency to oxidized the other substance.

It’s formed when a molecule or ions loose its electron.

Common oxidizing agents are oxygen, hydrogen peroxide, and halogens.

Redox reaction: redox reaction is that type of reaction where both oxidation and reduction takes place.

This is the popular Aromatic electrophilic substitution reaction and are classified into two types

1-Friedel Craft Alkylation:-It involves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid catalyst with anhydrous Ferrichloride as a catalyst and thhe alkyl group attached at the former site of the chloride ion.

2-Fridel Craft Acylation: - It involves the acylation of aromatic rings with an acyl chloride using a strong Lewis acid catalyst. Like AlCl3 catalyst.

c)

Interpretation Introduction

Interpretation:

To determine the necessary reagent to achieve the following transformation.

Concept Introduction:

Reagent: it is a substance or compound added to a chemical reaction and which donates a chemical ingredient (a compound of mixture, typically of organic or inorganic substance.

Examples include the Collins reagent, Fenton’s reagent and the most popular Grignard’s reagent etc…

Ozonolysis: it’s an organic reaction where the unsaturated bonds alkanes and alkynes compounds are broken with ozone.

Alkenes and alkynes form organic compound, which have multiple carbon-carbon bond and it has been replaced by a carbonyl group.

Oxidizing reagent: it’s composed of oxidant and oxidizer. It has a tendency to oxidized the other substance.

It’s formed when a molecule or ions loose its electron.

Common oxidizing agents are oxygen, hydrogen peroxide, and halogens.

Redox reaction: redox reaction is that type of reaction where both oxidation and reduction takes place.

This is the popular Aromatic electrophilic substitution reaction and are classified into two types

1-Friedel Craft Alkylation:-It involves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid catalyst with anhydrous Ferrichloride as a catalyst and thhe alkyl group attached at the former site of the chloride ion.

2-Fridel Craft Acylation: - It involves the acylation of aromatic rings with an acyl chloride using a strong Lewis acid catalyst. Like AlCl3 catalyst.

d)

Interpretation Introduction

Interpretation:

To determine the necessary reagent to achieve the following transformation.

Concept Introduction:

Reagent: it is a substance or compound added to a chemical reaction and which donates a chemical ingredient (a compound of mixture, typically of organic or inorganic substance.

Examples include the Collins reagent, Fenton’s reagent and the most popular Grignard’s reagent etc…

Ozonolysis: it’s an organic reaction where the unsaturated bonds alkanes and alkynes compounds are broken with ozone.

Alkenes and alkynes form organic compound, which have multiple carbon-carbon bond and it has been replaced by a carbonyl group.

Oxidizing reagent: it’s composed of oxidant and oxidizer. It has a tendency to oxidized the other substance.

It’s formed when a molecule or ions loose its electron.

Common oxidizing agents are oxygen, hydrogen peroxide, and halogens.

Redox reaction: redox reaction is that type of reaction where both oxidation and reduction takes place.

This is the popular Aromatic electrophilic substitution reaction and are classified into two types

1-Friedel Craft Alkylation:-It involves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid catalyst with anhydrous Ferrichloride as a catalyst and thhe alkyl group attached at the former site of the chloride ion.

2-Fridel Craft Acylation: - It involves the acylation of aromatic rings with an acyl chloride using a strong Lewis acid catalyst. Like AlCl3 catalyst.

e)

Interpretation Introduction

Interpretation:

To determine the necessary reagent to achieve the following transformation.

Concept Introduction:

Reagent: it is a substance or compound added to a chemical reaction and which donates a chemical ingredient (a compound of mixture, typically of organic or inorganic substance.

Examples include the Collins reagent, Fenton’s reagent and the most popular Grignard’s reagent etc…

Ozonolysis: it’s an organic reaction where the unsaturated bonds alkanes and alkynes compounds are broken with ozone.

Alkenes and alkynes form organic compound, which have multiple carbon-carbon bond and it has been replaced by a carbonyl group.

Oxidizing reagent: it’s composed of oxidant and oxidizer. It has a tendency to oxidized the other substance.

It’s formed when a molecule or ions loose its electron.

Common oxidizing agents are oxygen, hydrogen peroxide, and halogens.

Redox reaction: redox reaction is that type of reaction where both oxidation and reduction takes place.

This is the popular Aromatic electrophilic substitution reaction and are classified into two types

1-Friedel Craft Alkylation:-It involves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid catalyst with anhydrous Ferrichloride as a catalyst and thhe alkyl group attached at the former site of the chloride ion.

2-Fridel Craft Acylation: - It involves the acylation of aromatic rings with an acyl chloride using a strong Lewis acid catalyst. Like AlCl3 catalyst.

f)

Interpretation Introduction

Interpretation:

To determine the necessary reagent to achieve the following transformation.

Concept Introduction:

Reagent: it is a substance or compound added to a chemical reaction and which donates a chemical ingredient (a compound of mixture, typically of organic or inorganic substance.

Examples include the Collins reagent, Fenton’s reagent and the most popular Grignard’s reagent etc…

Ozonolysis: it’s an organic reaction where the unsaturated bonds alkanes and alkynes compounds are broken with ozone.

Alkenes and alkynes form organic compound, which have multiple carbon-carbon bond and it has been replaced by a carbonyl group.

Oxidizing reagent: it’s composed of oxidant and oxidizer. It has a tendency to oxidized the other substance.

It’s formed when a molecule or ions loose its electron.

Common oxidizing agents are oxygen, hydrogen peroxide, and halogens.

Redox reaction: redox reaction is that type of reaction where both oxidation and reduction takes place.

This is the popular Aromatic electrophilic substitution reaction and are classified into two types

1-Friedel Craft Alkylation:-It involves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid catalyst with anhydrous Ferrichloride as a catalyst and thhe alkyl group attached at the former site of the chloride ion.

2-Fridel Craft Acylation: - It involves the acylation of aromatic rings with an acyl chloride using a strong Lewis acid catalyst. Like AlCl3 catalyst.

Blurred answer

Chapter 19 Solutions

Organic Chemistry

Ch. 19.5 - Prob. 9ATSCh. 19.5 - Prob. 10CCCh. 19.5 - Prob. 11CCCh. 19.5 - Prob. 12CCCh. 19.5 - Prob. 13CCCh. 19.6 - Prob. 3LTSCh. 19.6 - Prob. 14PTSCh. 19.6 - Prob. 15PTSCh. 19.6 - Prob. 16ATSCh. 19.6 - Prob. 17CCCh. 19.6 - Prob. 18CCCh. 19.6 - Prob. 20PTSCh. 19.6 - Prob. 21ATSCh. 19.6 - Prob. 22CCCh. 19.7 - Prob. 5LTSCh. 19.7 - Prob. 23PTSCh. 19.7 - Prob. 24ATSCh. 19.7 - Prob. 25CCCh. 19.8 - Prob. 26CCCh. 19.8 - Prob. 27CCCh. 19.9 - Prob. 28CCCh. 19.9 - Prob. 29CCCh. 19.10 - Prob. 30CCCh. 19.10 - Prob. 31CCCh. 19.10 - Prob. 32CCCh. 19.10 - Prob. 33CCCh. 19.10 - Prob. 6LTSCh. 19.10 - Prob. 34PTSCh. 19.10 - Prob. 35PTSCh. 19.10 - Prob. 36ATSCh. 19.10 - Prob. 37ATSCh. 19.10 - Prob. 38CCCh. 19.11 - Prob. 39CCCh. 19.12 - Prob. 7LTSCh. 19.12 - Prob. 40PTSCh. 19.12 - Prob. 41ATSCh. 19.13 - Prob. 42CCCh. 19 - Prob. 43PPCh. 19 - Prob. 44PPCh. 19 - Prob. 45PPCh. 19 - Prob. 46PPCh. 19 - Prob. 47PPCh. 19 - Prob. 48PPCh. 19 - Prob. 49PPCh. 19 - Prob. 50PPCh. 19 - Prob. 51PPCh. 19 - Prob. 52PPCh. 19 - Prob. 53PPCh. 19 - Prob. 54PPCh. 19 - Prob. 55PPCh. 19 - Prob. 56PPCh. 19 - Prob. 57PPCh. 19 - Prob. 58PPCh. 19 - Prob. 59PPCh. 19 - Prob. 60PPCh. 19 - Predict the major product(s) obtained when each of...Ch. 19 - Prob. 62PPCh. 19 - Prob. 63PPCh. 19 - Prob. 64PPCh. 19 - Prob. 65PPCh. 19 - Prob. 66PPCh. 19 - Prob. 67PPCh. 19 - Prob. 68PPCh. 19 - Prob. 69PPCh. 19 - Prob. 70PPCh. 19 - Prob. 71PPCh. 19 - Prob. 72PPCh. 19 - Prob. 73PPCh. 19 - Prob. 74IPCh. 19 - Prob. 75IPCh. 19 - Prob. 76IPCh. 19 - Prob. 77IPCh. 19 - Prob. 78IPCh. 19 - Prob. 79IPCh. 19 - Prob. 80IPCh. 19 - Prob. 81IPCh. 19 - Prob. 83IPCh. 19 - Prob. 84IPCh. 19 - Prob. 85IPCh. 19 - Prob. 86IPCh. 19 - Prob. 87IPCh. 19 - Prob. 88IPCh. 19 - Prob. 89IPCh. 19 - Prob. 90IPCh. 19 - Prob. 91IPCh. 19 - Prob. 92IPCh. 19 - Prob. 93IPCh. 19 - Prob. 94CPCh. 19 - Prob. 95CPCh. 19 - Treatment of the following ketone with LiAIHa...
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