Organic Chemistry: Principles and Mechanisms (Second Edition)
Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
Question
Book Icon
Chapter 7, Problem 7.54P
Interpretation Introduction

(a)

Interpretation:

The electron-rich sites and electron-poor sites in the given elementary steps are to be identified.

Concept introduction:

An atom with partial or full negative charge is an electron-rich site whereas an atom with partial or full positive charge is an electron-poor site. In an elementary step, electrons tend to flow from an electron-rich site to an electron-poor site.

Expert Solution
Check Mark

Answer to Problem 7.54P

The electron-rich and electron-poor sites for first elementary step are:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  1

The electron-rich and electron-poor sites for second elementary step are:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  2

The electron-rich and electron-poor sites for third elementary step are:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  3

The electron-rich and electron-poor sites for fourth elementary step are:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  4

The electron-rich and electron-poor sites for fifth elementary step are:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  5

The electron-rich and electron-poor sites for sixth elementary step are:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  6

Explanation of Solution

The first elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  7

In the given elementary step, on the reactant side the oxygen atom which is a part carbonyl group having lone pairs is the electron-rich site. The hydrogen atom bonded to positively charged oxygen is the electron-poor site. The electron-rich and electron-poor sites for this step are labeled below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  8

The second elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  9

In this elementary step, the oxygen atom of water molecule with lone pairs is the electron-rich site. The carbon atom adjacent to positively charged oxygen is electron-poor site. The electron-rich and electron-poor sites for this step are labeled below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  10

The third elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  11

In this elementary step, the oxygen atom of water molecule with lone pairs is the electron-rich site. The H atom adjacent to positively charged oxygen is electron-poor site. The electron-rich and electron-poor sites for this step are labeled below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  12

The fourth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  13

In the given elementary step, on the reactant side the nitrogen atom having lone pairs is the electron-rich site. The hydrogen atom bonded to positively charged oxygen is the electron-poor site. The electron-rich and electron-poor sites for this step are labeled below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  14

The fifth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  15

In the given elementary step, on the reactant side the oxygen atom of C-O bond having lone pairs is the electron-rich site. The nitrogen atom which is positively charged is the electron-poor site. The electron-rich and electron-poor sites for this step are labeled below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  16

The sixth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  17

In the given elementary step, on the reactant side the hydrogen atom adjacent to positively charged oxygen atom is the electron-poor site. The nitrogen atom which is having lone pair of electrons is the electron-rich site. The electron-rich and electron-poor sites for this step are labeled below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  18

Conclusion

The electron-rich site and the electron-poor sites in each elementary step are identified on the basis of the negative and partial positive charge on respective atoms.

Interpretation Introduction

(b)

Interpretation:

In each of the given elementary steps the appropriate curved arrows are to be drawn.

Concept introduction:

The curved arrow can draw from electron rich site to an electron poor site to show the flow of electron from electron-rich site to electron-poor site. The first curved arrow drawn from the lone pair of negatively charged atom of electron-rich site to the less electronegative atom of electron-poor site. The second curved arrow drawn from the region between the less electronegative atom and more electronegative atom towards the more electronegative atom indicating the breaking of bond.

Expert Solution
Check Mark

Answer to Problem 7.54P

The curved arrow mechanism for the first step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  19

The curved arrow mechanism for the second step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  20

The curved arrow mechanism for the third step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  21

The curved arrow mechanism for the fourth step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  22

The curved arrow mechanism for the fifth step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  23

The curved arrow mechanism for the sixth step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  24

Explanation of Solution

The first elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  25

In above step the oxygen is an electron-rich site which attack at hydrogen atom bonded to positively charged oxygen atom is an electron poor site.

The curved arrow mechanism for this step is shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  26

The first curved arrow is drawn from the lone pair of electron-rich oxygen to the electron-poor hydrogen atom representing the formation of OH bond. The second curved arrow is drawn from the region between the electron-poor hydrogen and the positively charged oxygen towards the positively charged oxygen representing the breaking of OH bond and stabilized the positive charged on oxygen atom.

The second elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  27

In this elementary step, the oxygen atom of water molecule having lone pair is the electron-rich site and the carbon atom adjacent to positively charged oxygen atom is electron-poor site. The curved arrow mechanism for this step is shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  28

The first curved arrow is drawn from the lone pair of electron-rich oxygen atom to the electron-poor carbon atom representing the formation of new CO bond. The second curved arrow is drawn from the region between the electron-poor carbon and positively charged oxygen atom towards the positively charged oxygen atom.

The third elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  29

In this elementary step, the oxygen atom of water molecule with lone pairs is the electron-rich site. The hydrogen atom bonded to positively charged oxygen is an electron-poor site. The curved arrow mechanism for this step is shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  30

The first curved arrow is drawn from the lone pair of electron-rich oxygen atom of water to the electron-poor hydrogen atom representing the formation of new O-H bond. The second curved arrow is drawn from the region between the electron-poor hydrogen and positively charged oxygen atom towards the positively charged oxygen atom.

The fourth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  31

In the given elementary step, on the reactant side the nitrogen atom having lone pairs is the electron-rich site. The hydrogen atom bonded to positively charged oxygen is the electron-poor site. The curved arrow mechanism for this step is shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  32

The first curved arrow is drawn from the lone pair of electron-rich nitrogen to the electron-poor hydrogen atom representing the formation of N-H bond. The second curved arrow is drawn from the region between the electron-poor hydrogen and the positively charged oxygen towards the positively charged oxygen representing the breaking of OH bond and stabilized the positive charged on oxygen atom.

The fifth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  33

In the given elementary step, on the reactant side the oxygen atom of C-O bond having lone pairs is the electron-rich site. The nitrogen atom which is positively charged is the electron-poor site. The curved arrow mechanism for this step is shown below:Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  34

The first curved arrow is drawn from the lone pair of electron-rich oxygen to the C-O bond representing the formation a bond. The second curved arrow is drawn from the region between C-N bond and the positively charged nitrogen towards the positively charged nitrogen representing the breaking of C-N bond and stabilized the positive charged on nitrogen atom.

The sixth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  35

In the given elementary step, on the reactant side the hydrogen atom adjacent to positively charged oxygen atom is the electron-poor site. The nitrogen atom which is having lone pair of electrons is the electron-rich site. The curved arrow mechanism for this step is shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  36

The first curved arrow is drawn from the lone pair of electron-rich nitrogen to the electron-poor hydrogen atom representing the formation of N-H bond. The second curved arrow is drawn from the region between the electron-poor hydrogen and the positively charged oxygen towards the positively charged oxygen representing the breaking of OH bond and stabilized the positive charged on oxygen atom.

Conclusion

The curved arrows for each of the given elementary steps are drawn from electron rich site to electron poor site and the less electronegative atom to more electronegative atom representing the formation and breaking of respective bonds.

Interpretation Introduction

(c)

Interpretation:

The names of each elementary step are to be identified.

Concept introduction:

In the nucleophilic addition step, the nucleophile forms a bond to the less electronegative atom and the π bond breaks, becoming a lone pair on the more electronegative atom.

In a nucleophilic elimination step, a lone pair of electrons from a more electronegative atom forms a π bond to a less electronegative atom. A leaving group is simultaneously expelled to avoid exceeding an octet on the less electronegative atom.

An elementary step in which a proton is transferred from electron-poor site to electron- rich site and one bond is broken and another is formed simultaneously is called proton transfer step.

Expert Solution
Check Mark

Answer to Problem 7.54P

The first elementary step is proton transfer reaction.

The nucleophilic addition reaction is the second elementary step.

The third elementary step is proton transfer reaction.

The fourth elementary step is proton transfer reaction.

The fifth elementary step is nucleophilic elimination reaction.

The sixth elementary step is proton transfer reaction.

Explanation of Solution

The first elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  37

In the above elementary step, proton transferred from the positively charged oxygen of water molecule to the electron-rich oxygen atom. In this step, one OH bond of water molecule is broken and the new OH bond is formed. As the step involved transfer of proton from electron-poor atom to electron-rich atom, the step is named as proton transfer reaction.

The second elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  38

In the above elementary step, the oxygen atom of water forms a bond to the less electronegative carbon atom and the C=Oπ bond breaks, becoming a lone pair on the more electronegative oxygen atom. Therefore, the step is named as nucleophilic addition step.

The third elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  39

In the above elementary step, proton transferred from the positively charged oxygen of to the electron-rich oxygen atom of water molecule. In this step, one OH bond is broken and the new OH bond in water molecule is formed. As the step involved transfer of proton from electron-poor atom to electron-rich atom, the step is named as proton transfer reaction.

The fourth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  40

In the above elementary step, proton transferred from the positively charged oxygen of water molecule to the electron-rich nitrogen atom. In this step, one OH bond of water molecule is broken and the new N-H bond is formed. As the step involved transfer of proton from electron-poor atom to electron-rich atom, the step is named as proton transfer reaction.

The fifth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  41

In the above elementary step, a lone pair of electrons from oxygen atom forms a π bond to a less electronegative carbon atom. A leaving group is simultaneously expelled to avoid exceeding an octet on the less electronegative carbon atom. Therefore, the step is named as nucleophilic elimination step.

The sixth elementary step is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.54P , additional homework tip  42

In the above elementary step, proton transferred from the positively charged oxygen of to the electron-rich nitrogen atom. In this step, one OH bond is broken and the new N-H bond is formed. As the step involved transfer of proton from electron-poor atom to electron-rich atom, the step is named as proton transfer reaction.

Conclusion

The names for the given elementary steps are identified on the basis of type of bond forming and breaking.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
The reaction shown here, which converts an epoxide into a bromohydrin, is discussed in Chapter 10. It consists of the two elementary steps shown. For each step (i and ii), (a) identify all electron-rich sites and all electron-poor sites, (i) H H-Br BrO + H3C (b) draw in the appropriate curved arrows to show the bond formation and bond breaking that occur, and (c) name the elementary step. (i) BrO Но H3C H3C Br
The reaction shown here, which is discussed (i) OH OH, in Chapter 8, is an example of a unimolecular elimination (E1) reaction and consists of the three elementary steps shown. For each step (i-ii), (a) identify all electron-rich sites and all electron-poor sites, (b) draw in the appropriate Н-ОСН, CH,CH3 H-OCH,CH3 H curved arrows to show the bond formation and bond breaking that occur, and (c) name the elementary step. (ii) OH2 + H,O (ii) .H + H-OCH,CH3 H-ỘCH,CH3 > H
Shown here is an example of an electrophilic (i) CI aromatic substitution reaction, which we examine in Chapter 22. The mechanism consists of the four elementary steps shown. For each step (i–iv), (a) identify all electron-rich sites and all electron-poor sites, (b) draw in the appropriate curved arrows to show the bond formation and bond breaking that occur, and (c) name the elementary step. CI-CI + Fe CI (ii) CI CI (iii) CI (iv) CI CI + H,O H00

Chapter 7 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Organic Chemistry: A Guided Inquiry
    Chemistry
    ISBN:9780618974122
    Author:Andrei Straumanis
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning