It should be determined that whether an organolithium compound or organosodium compound is more reactive. Concept Introduction: Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction. Electrophilic reaction: The aromatic substitution involves the attack on the electrophile by the π − e l e c t r o n of the aromatic ring and replacing one of the hydrogen molecules on the ring (or) respective species. Reactivity of organometallic compound : The reactivity of an organometallic compound depends on the polarity of the carbon-metal bond, the greater the polarity of the bond, the more reactive the compound is as a nucleophile, the polarity of the bond on the difference in electronegativity between the metal and carbon atom. Organolithium: Organolithium compounds are very strong base, therefore they will react immediately with any acid present in the reaction mixture, even with very week acids such as water and alcohol. Organosodium: Organosodium compound are less base when compare to the organo lithium compound because, organosodium compounds have less electronegative character.

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Chapter 12, Problem 2P

Interpretation Introduction

Interpretation:

It should be determined that whether an organolithium compound or organosodium compound is more reactive.

Concept Introduction:

Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.

Electrophilic reaction: The aromatic substitution involves the attack on the electrophile by the π−electron of the aromatic ring and replacing one of the hydrogen molecules on the ring (or) respective species.

Reactivity of organometallic compound: The reactivity of an organometallic compound depends on the polarity of the carbon-metal bond, the greater the polarity of the bond, the more reactive the compound is as a nucleophile, the polarity of the bond on the difference in electronegativity between the metal and carbon atom.

Organolithium: Organolithium compounds are very strong base, therefore they will react immediately with any acid present in the reaction mixture, even with very week acids such as water and alcohol.

Organosodium: Organosodium compound are less base when compare to the organo lithium compound because, organosodium compounds have less electronegative character.

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Answer 2

Question

Chapter 12, Problem 2P

Interpretation Introduction

Interpretation:

It should be determined that whether an organolithium compound or organosodium compound is more reactive.

Concept Introduction:

Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.

Electrophilic reaction: The aromatic substitution involves the attack on the electrophile by the π−electron of the aromatic ring and replacing one of the hydrogen molecules on the ring (or) respective species.

Reactivity of organometallic compound: The reactivity of an organometallic compound depends on the polarity of the carbon-metal bond, the greater the polarity of the bond, the more reactive the compound is as a nucleophile, the polarity of the bond on the difference in electronegativity between the metal and carbon atom.

Organolithium: Organolithium compounds are very strong base, therefore they will react immediately with any acid present in the reaction mixture, even with very week acids such as water and alcohol.

Organosodium: Organosodium compound are less base when compare to the organo lithium compound because, organosodium compounds have less electronegative character.

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Answer 3

Question

Chapter 12, Problem 2P

Interpretation Introduction

Interpretation:

It should be determined that whether an organolithium compound or organosodium compound is more reactive.

Concept Introduction:

Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.

Electrophilic reaction: The aromatic substitution involves the attack on the electrophile by the π−electron of the aromatic ring and replacing one of the hydrogen molecules on the ring (or) respective species.

Reactivity of organometallic compound: The reactivity of an organometallic compound depends on the polarity of the carbon-metal bond, the greater the polarity of the bond, the more reactive the compound is as a nucleophile, the polarity of the bond on the difference in electronegativity between the metal and carbon atom.

Organolithium: Organolithium compounds are very strong base, therefore they will react immediately with any acid present in the reaction mixture, even with very week acids such as water and alcohol.

Organosodium: Organosodium compound are less base when compare to the organo lithium compound because, organosodium compounds have less electronegative character.

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Answer 4

Question

Chapter 12, Problem 2P

Interpretation Introduction

Interpretation:

It should be determined that whether an organolithium compound or organosodium compound is more reactive.

Concept Introduction:

Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.

Electrophilic reaction: The aromatic substitution involves the attack on the electrophile by the π−electron of the aromatic ring and replacing one of the hydrogen molecules on the ring (or) respective species.

Reactivity of organometallic compound: The reactivity of an organometallic compound depends on the polarity of the carbon-metal bond, the greater the polarity of the bond, the more reactive the compound is as a nucleophile, the polarity of the bond on the difference in electronegativity between the metal and carbon atom.

Organolithium: Organolithium compounds are very strong base, therefore they will react immediately with any acid present in the reaction mixture, even with very week acids such as water and alcohol.

Organosodium: Organosodium compound are less base when compare to the organo lithium compound because, organosodium compounds have less electronegative character.

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Answer 5

Chapter 12, Problem 2P

Interpretation Introduction

Interpretation:

It should be determined that whether an organolithium compound or organosodium compound is more reactive.

Concept Introduction:

Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.

Electrophilic reaction: The aromatic substitution involves the attack on the electrophile by the π−electron of the aromatic ring and replacing one of the hydrogen molecules on the ring (or) respective species.

Reactivity of organometallic compound: The reactivity of an organometallic compound depends on the polarity of the carbon-metal bond, the greater the polarity of the bond, the more reactive the compound is as a nucleophile, the polarity of the bond on the difference in electronegativity between the metal and carbon atom.

Organolithium: Organolithium compounds are very strong base, therefore they will react immediately with any acid present in the reaction mixture, even with very week acids such as water and alcohol.

Organosodium: Organosodium compound are less base when compare to the organo lithium compound because, organosodium compounds have less electronegative character.

Answer 6

Chapter 12, Problem 2P

Interpretation Introduction

Interpretation:

It should be determined that whether an organolithium compound or organosodium compound is more reactive.

Concept Introduction:

Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.

Electrophilic reaction: The aromatic substitution involves the attack on the electrophile by the π−electron of the aromatic ring and replacing one of the hydrogen molecules on the ring (or) respective species.

Reactivity of organometallic compound: The reactivity of an organometallic compound depends on the polarity of the carbon-metal bond, the greater the polarity of the bond, the more reactive the compound is as a nucleophile, the polarity of the bond on the difference in electronegativity between the metal and carbon atom.

Organolithium: Organolithium compounds are very strong base, therefore they will react immediately with any acid present in the reaction mixture, even with very week acids such as water and alcohol.

Organosodium: Organosodium compound are less base when compare to the organo lithium compound because, organosodium compounds have less electronegative character.

Answer 7

Chapter 12, Problem 2P

Interpretation Introduction

Interpretation:

It should be determined that whether an organolithium compound or organosodium compound is more reactive.

Concept Introduction:

Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.

Electrophilic reaction: The aromatic substitution involves the attack on the electrophile by the π−electron of the aromatic ring and replacing one of the hydrogen molecules on the ring (or) respective species.

Reactivity of organometallic compound: The reactivity of an organometallic compound depends on the polarity of the carbon-metal bond, the greater the polarity of the bond, the more reactive the compound is as a nucleophile, the polarity of the bond on the difference in electronegativity between the metal and carbon atom.

Organolithium: Organolithium compounds are very strong base, therefore they will react immediately with any acid present in the reaction mixture, even with very week acids such as water and alcohol.

Organosodium: Organosodium compound are less base when compare to the organo lithium compound because, organosodium compounds have less electronegative character.

Answer 8

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Answer 11

Ch. 12.1 - Prob. 1P Ch. 12.2 - Which is more reactive an organolithium compound...Ch. 12.2 - Prob. 3P Ch. 12.3 - PROBLEM 6♦ Explain why tertiary alkyl halides...Ch. 12.3 - Muscalure is the sex attractant of the common...Ch. 12.3 - Prob. 8P Ch. 12.3 - Prob. 9P Ch. 12.3 - Prob. 10P Ch. 12.4 - Prob. 13P Ch. 12.4 - Prob. 14P

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