Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+)
Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+)
3rd Edition
ISBN: 9780137533268
Author: Paula Bruice
Publisher: PEARSON+
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Chapter 6, Problem 49P

(a)

Interpretation Introduction

Interpretation:

The given compound should be prepared using alkene and other reagents.

Concept Introduction:

Addition ofH2:

Catalytic hydrogenation in presence of Pd/C is an example for syn addition of hydrogen.

Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+), Chapter 6, Problem 49P , additional homework tip  1

For cyclic reactants, the addition of H2 will form cis enantiomers since two hydrogens adds to one side of the double bond.

Enantiomers: they are chiral molecules whose mirror images are not superimposable.

Enantiomers are given configuration as R or S based on the atoms bonded with chiral (carbon bonded with four different substituents) carbon.

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

Carbocation stability order:

Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+), Chapter 6, Problem 49P , additional homework tip  2

Nucleophile: It donates pair of electrons to positively charged substrate resulting in the formation of chemical bond.

Electrophile: It is positively charged species which seeks for negative charge and hence accepts pair of electrons from negatively charged species (Nucleophiles) which results in the formation of chemical bond.

(b)

Interpretation Introduction

Interpretation:

The given compound should be prepared using alkene and other reagents.

Concept Introduction:

Addition ofH2:

Catalytic hydrogenation in presence of Pd/C is an example for syn addition of hydrogen.

Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+), Chapter 6, Problem 49P , additional homework tip  3

For cyclic reactants, the addition of H2 will form cis enantiomers since two hydrogens adds to one side of the double bond.

Enantiomers: they are chiral molecules whose mirror images are not superimposable.

Enantiomers are given configuration as R or S based on the atoms bonded with chiral (carbon bonded with four different substituents) carbon.

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

Carbocation stability order:

Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+), Chapter 6, Problem 49P , additional homework tip  4

Nucleophile: It donates pair of electrons to positively charged substrate resulting in the formation of chemical bond.

Electrophile: It is positively charged species which seeks for negative charge and hence accepts pair of electrons from negatively charged species (Nucleophiles) which results in the formation of chemical bond.

(c)

Interpretation Introduction

Interpretation:

The given compound should be prepared using alkene and other reagents.

Concept Introduction:

Addition of hydrogen halides:

In the addition of hydrogen halides over alkenes, first the H+ gets bonded to carbon and forms most stable carbocation which then the halide ion bonds with carbocation that results in formation of product.

Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+), Chapter 6, Problem 49P , additional homework tip  5

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

Carbocation stability order:

Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+), Chapter 6, Problem 49P , additional homework tip  6

Nucleophile: It donates pair of electrons to positively charged substrate resulting in the formation of chemical bond.

Electrophile: It is positively charged species which seeks for negative charge and hence accepts pair of electrons from negatively charged species (Nucleophiles) which results in the formation of chemical bond.

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Relative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 20 NaоH 0103 Br (B) H2504 → (c) (A) 100- MS-NU-0547 80 40 20 31 10 20 100- MS2016-05353CM 80 60 100 MS-NJ-09-3 80 60 40 20 45 J.L 80 S1 84 M+ absent राग 135 137 S2 62 164 166 11 S3 25 50 75 100 125 150 175 m/z
Don't used hand raiting and don't used Ai solution
Don't used hand raiting

Chapter 6 Solutions

Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+)

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