EBK ESSENTIAL ORGANIC CHEMISTRY
EBK ESSENTIAL ORGANIC CHEMISTRY
3rd Edition
ISBN: 9780100659469
Author: Bruice
Publisher: YUZU
Question
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Chapter 6, Problem 31P

(a)

Interpretation Introduction

Interpretation:

The major product for reaction between 2-methyl-2-butene with given reagent should be determined.

Concept introduction:

Nucleophile: Nucleophiles are electron rich compounds which donates electrons to electrophilic compounds which results in bond formation.

Electrophile: Electrophiles are electron deficient compounds which accepts electrons from nucleophiles that results in bond formation.

Electrophilic addition: It is a type of addition reaction in which the pi bond present in the molecule breaks as the electrophile approaches and results in the formation of product with sigma bond.

Oxidation Reaction: It involves loss of electrons, addition of oxygen atoms or removal of hydrogen atoms.

Reduction Reaction: It is just opposite of oxidation reaction which involves removal of oxygen atoms or addition of hydrogen atoms and addition of electrons.

Carbocation: it is carbon ion that bears a positive charge on it.

Carbocation stability order:

  EBK ESSENTIAL ORGANIC CHEMISTRY, Chapter 6, Problem 31P , additional homework tip  1

(b)

Interpretation Introduction

Interpretation:

The major product for reaction between 2-methyl-2-butene with given reagent should be determined.

Concept introduction:

Nucleophile: Nucleophiles are electron rich compounds which donates electrons to electrophilic compounds which results in bond formation.

Electrophile: Electrophiles are electron deficient compounds which accepts electrons from nucleophiles that results in bond formation.

Electrophilic addition: It is a type of addition reaction in which the pi bond present in the molecule breaks as the electrophile approaches and results in the formation of product with sigma bond.

Oxidation Reaction: It involves loss of electrons, addition of oxygen atoms or removal of hydrogen atoms.

Reduction Reaction: It is just opposite of oxidation reaction which involves removal of oxygen atoms or addition of hydrogen atoms and addition of electrons.

Carbocation: it is carbon ion that bears a positive charge on it.

Carbocation stability order:

  EBK ESSENTIAL ORGANIC CHEMISTRY, Chapter 6, Problem 31P , additional homework tip  2

(c)

Interpretation Introduction

Interpretation:

The major product for reaction between 2-methyl-2-butene with given reagent should be determined.

Concept introduction:

Nucleophile: Nucleophiles are electron rich compounds which donates electrons to electrophilic compounds which results in bond formation.

Electrophile: Electrophiles are electron deficient compounds which accepts electrons from nucleophiles that results in bond formation.

Electrophilic addition: It is a type of addition reaction in which the pi bond present in the molecule breaks as the electrophile approaches and results in the formation of product with sigma bond.

Addition of halogen to an alkene: The addition of halogen to an alkene compound forms cyclic 3 membered intermediate as the first step which then the leads to the product formation. Example for this is as follows,

  EBK ESSENTIAL ORGANIC CHEMISTRY, Chapter 6, Problem 31P , additional homework tip  3

(d)

Interpretation Introduction

Interpretation:

The major product for reaction between 2-methyl-2-butene with given reagent should be determined.

Concept introduction:

Nucleophile: Nucleophiles are electron rich compounds which donates electrons to electrophilic compounds which results in bond formation.

Electrophile: Electrophiles are electron deficient compounds which accepts electrons from nucleophiles that results in bond formation.

Electrophilic addition: It is a type of addition reaction in which the pi bond present in the molecule breaks as the electrophile approaches and results in the formation of product with sigma bond.

Oxidation Reaction: It involves loss of electrons, addition of oxygen atoms or removal of hydrogen atoms.

Acid Catalyzed Hydration Reaction: The reaction involves breaking of phi bonds between carbon-carbon multiple bonds and addition of alcohol to more substituted position of carbon in the molecule.

First step is the acid donates proton to the alkene which leads to the formation of more stable carbo cation.

Then, the water is added to the given alkene through acid catalyzed reaction where the water gets added to the carbo cation finally, the removal of one proton from oxonium ion (oxygen with one positive charge) using water results in the formation of product.

Carbocation: it is carbon ion that bears a positive charge on it.

Carbocation stability order:

  EBK ESSENTIAL ORGANIC CHEMISTRY, Chapter 6, Problem 31P , additional homework tip  4

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Chapter 6 Solutions

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