ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
3rd Edition
ISBN: 9781119497479
Author: Klein
Publisher: WILEY
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Chapter 18, Problem 67PP

(a)

Interpretation Introduction

Interpretation:

Synthesis of the given compound has to be proposed using benzene as starting material.

Concept Introduction:

Benzene is an electron rich aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Halogenation: In halogenation reaction, hydrogen atom of a molecule is replaced by a halogen atom (F,Cl,Br,I) .

Nitration: in nitration reaction, one nitro group (NO2) is introduced to an organic molecule. Mixture of nitric acid and sulfuric acid is used for nitration.

(b)

Interpretation Introduction

Interpretation: Synthesis of the given compound has to be proposed using benzene as starting material.

Concept Introduction:

Benzene is an electron rich aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Nitration: in nitration reaction, one nitro group (NO2) is introduced to an organic molecule. Mixture of nitric acid and sulfuric acid is used for nitration.

Oxidation: If - oxygen atoms are added to a species or hydrogen atom gets removed from a species during a chemical reaction is known as oxidation.

(c)

Interpretation Introduction

Interpretation: Synthesis of the given compound has to be proposed using benzene as starting material.

Concept Introduction:

Benzene is an electron rich aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Nitration: in nitration reaction, one nitro group (NO2) is introduced to an organic molecule. Mixture of nitric acid and sulfuric acid is used for nitration.

Halogenation: In halogenation reaction, hydrogen atom of a molecule is replaced by a halogen atom (F,Cl,Br,I) .

(d)

Interpretation Introduction

Interpretation: Synthesis of the given compound has to be proposed using benzene as starting material.

Concept Introduction:

Benzene is an electron rich aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Friedel-Crafts Acylation: This Lewis acid-catalyzed electrophilic aromatic substitution is the reaction between arenes and acyl chlorides or anhydrides for the synthesis of monoacylated compound. The products are deactivated, as well as do not undergo a second substitution.

Chlorination: In chlorination reaction, hydrogen atom of a molecule is replaced by a chlorine atom.

Nitration: in nitration reaction, one nitro group (NO2) is introduced to an organic molecule. Mixture of nitric acid and sulfuric acid is used for nitration.

(e)

Interpretation Introduction

Interpretation: Synthesis of the given compound has to be proposed using benzene as starting material.

Concept Introduction:

Benzene is an electron rich aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Nitration: in nitration reaction, one nitro group (NO2) is introduced to an organic molecule. Mixture of nitric acid and sulfuric acid is used for nitration.

Oxidation: If electrons are moved from a species or oxygen atoms are added to a species or hydrogen atom gets removed from a species during a chemical reaction is known as reduction.

Bromination: In bromination reaction, hydrogen atom of a molecule is replaced by a bromine atom.

Chlorination: In chlorination reaction, hydrogen atom of a molecule is replaced by a chlorine atom.

(f)

Interpretation Introduction

Interpretation: Synthesis of the given compound has to be proposed using benzene as starting material.

Concept Introduction:

Benzene is an electron rich aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Nucleophilic aromatic substitution reaction: SNAr reaction is a substitution reaction occurs on an aromatic ring where a good leaving group on it is displaced by a nucleophile.

Nitration: in nitration reaction, one nitro group (NO2) is introduced to an organic molecule. Mixture of nitric acid and sulfuric acid is used for nitration.

Chlorination: In chlorination reaction, hydrogen atom of a molecule is replaced by a chlorine atom.

(g)

Interpretation Introduction

Interpretation: Synthesis of the given compound has to be proposed using benzene as starting material.

Concept Introduction:

Benzene is an electron rich aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Nitration: in nitration reaction, one nitro group (NO2) is introduced to an organic molecule. Mixture of nitric acid and sulfuric acid is used for nitration.

Halogenation: In halogenation reaction, hydrogen atom of a molecule is replaced by a halogen atom (F,Cl,Br,I) .

(h)

Interpretation Introduction

Interpretation: Synthesis of the given compound has to be proposed using benzene as starting material.

Concept Introduction:

Benzene is an electron rich aromatic compound. It undergoes aromatic electrophilic substitution reaction.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic aromatic replacement allows the synthesis of alkylated products by means of the reaction of arenes through alkyl halides or alkenes.

Nitration: in nitration reaction, one nitro group (NO2) is introduced to an organic molecule. Mixture of nitric acid and sulfuric acid is used for nitration.

Bromination: In bromination reaction, hydrogen atom of a molecule is replaced by a bromine atom.

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Chapter 18 Solutions

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)

Ch. 18.7 - Prob. 11CCCh. 18.7 - Prob. 12CCCh. 18.8 - Prob. 13CCCh. 18.9 - Prob. 14CCCh. 18.9 - Prob. 15CCCh. 18.10 - Prob. 1LTSCh. 18.10 - Prob. 16PTSCh. 18.11 - Prob. 2LTSCh. 18.11 - Prob. 18PTSCh. 18.11 - Prob. 19ATSCh. 18.11 - Prob. 3LTSCh. 18.11 - Prob. 20PTSCh. 18.11 - Prob. 21ATSCh. 18.11 - Prob. 4LTSCh. 18.11 - Prob. 22PTSCh. 18.11 - Prob. 23ATSCh. 18.12 - Prob. 24CCCh. 18.12 - Prob. 25CCCh. 18.12 - Prob. 5LTSCh. 18.12 - Prob. 26PTSCh. 18.12 - 2-Nitroaniline has been used as a precursor in the...Ch. 18.12 - Prob. 6LTSCh. 18.12 - Prob. 28PTSCh. 18.12 - Prob. 29ATSCh. 18.13 - Prob. 30CCCh. 18.13 - Prob. 31CCCh. 18.13 - Prob. 32CCCh. 18.14 - Prob. 33CCCh. 18.14 - Prob. 34CCCh. 18.15 - Prob. 7LTSCh. 18.15 - Prob. 35PTSCh. 18.15 - Prob. 36PTSCh. 18 - Prob. 38PPCh. 18 - Prob. 39PPCh. 18 - Prob. 40PPCh. 18 - Prob. 41PPCh. 18 - Prob. 42PPCh. 18 - Prob. 43PPCh. 18 - Prob. 44PPCh. 18 - Prob. 45PPCh. 18 - Prob. 46PPCh. 18 - Prob. 47PPCh. 18 - Prob. 48PPCh. 18 - Prob. 49PPCh. 18 - Prob. 50PPCh. 18 - Prob. 51PPCh. 18 - Prob. 52PPCh. 18 - Prob. 53PPCh. 18 - Prob. 54PPCh. 18 - Prob. 55PPCh. 18 - Prob. 56PPCh. 18 - Prob. 57PPCh. 18 - Prob. 58PPCh. 18 - Prob. 59PPCh. 18 - Prob. 60PPCh. 18 - Prob. 61PPCh. 18 - Prob. 62PPCh. 18 - Prob. 63PPCh. 18 - Prob. 64PPCh. 18 - When 2,4-dibromo-3-methyltolene is treated with...Ch. 18 - Prob. 66PPCh. 18 - Prob. 67PPCh. 18 - Prob. 68PPCh. 18 - Prob. 69PPCh. 18 - Prob. 70PPCh. 18 - Prob. 71PPCh. 18 - Prob. 72PPCh. 18 - Prob. 74IPCh. 18 - Prob. 75IPCh. 18 - Prob. 76IPCh. 18 - Prob. 77IPCh. 18 - Prob. 78IPCh. 18 - Prob. 79IPCh. 18 - Prob. 80IPCh. 18 - Prob. 81IPCh. 18 - Prob. 82IPCh. 18 - Prob. 83IPCh. 18 - Prob. 84IPCh. 18 - Prob. 85IPCh. 18 - Prob. 86IPCh. 18 - Prob. 87IPCh. 18 - Prob. 88IPCh. 18 - Prob. 89IPCh. 18 - Prob. 90IPCh. 18 - Prob. 91CPCh. 18 - Prob. 92CPCh. 18 - In the following reaction, iodine monochloride...Ch. 18 - Prob. 94CPCh. 18 - The following synthesis was developed in an...
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