ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS
ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS
2nd Edition
ISBN: 9780393666151
Author: KARTY
Publisher: NORTON
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Question
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Chapter 6, Problem 6.39P
Interpretation Introduction

(a)

Interpretation:

Missing curved arrows are to be supplied for the given proton transfer reaction. The relevant electrons are to be drawn if they are not shown.

Concept introduction:

In a proton transfer reaction, a proton is transferred from a Bronsted-Lowry acid to a Bronsted-Lowry base in a single elementary step in which one bond is broken and another is formed simultaneously. The curved arrow notation shows the movement of valence electrons, not atoms. The movement of two electrons is shown be using a double-barbed arrow. To represent bond breaking, the tail of the arrow originates from the center of a bond whereas to represent bond formation, the head of arrow points to an atom which forms the new bond, that is, σ bond or the region where the bond is formed if the new bond is a π bond.

Expert Solution
Check Mark

Answer to Problem 6.39P

The missing curved arrow notation for the proton transfer reaction and relevant electrons is shown as

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  1

Explanation of Solution

The given proton transfer reaction is

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  2

In the above reaction, the bond (C-H) is formed between the C of the first reactant and H of water. Also, H2O donates a proton and forms its conjugate base, i.e., HO-, so one O-H bond of H2O is broken. The bond breaking and bond formation involve only valence electrons, so first all valence electrons in the given two reactants should be drawn. From that, it is clearly seen which electrons are involved in the reaction, both from the reactants and from the products, as shown below:

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  3

The appropriate movement of these valence electrons is shown by using curved arrow notations. One curved arrow is to be drawn from the lone pair on C to the H on water (highlighted blue) to illustrate the formation of H-C bond. A second curved arrow originates from the center of the O-H bond to illustrate the breaking of that bond and points to the O atom, showing that those electrons end up as a lone pair on O. Therefore, the curved arrow notation for the proton transfer reaction is as follows:

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  4

Conclusion

The curved arrow notation for the proton transfer of the given reaction is drawn on the basis of the movement of valence electrons involved in bond breaking and bond formation.

Interpretation Introduction

(b)

Interpretation:

Missing curved arrows are to be supplied for the given proton transfer reaction. The relevant electrons are to be drawn if they are not shown.

Concept introduction:

In a proton transfer reaction, a proton is transferred from a Bronsted-Lowry acid to a Bronsted-Lowry base in a single elementary step in which one bond is broken and another is formed simultaneously. The curved arrow notation shows the movement of valence electrons, not atoms. The movement of two electrons is shown be using a double-barbed arrow. To represent bond breaking, the tail of the arrow originates from the center of a bond whereas to represent bond formation, the head of arrow points to an atom which forms the new bond, that is, ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  5bond or the region where the bond is formed if the new bond is a ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  6bond.

Expert Solution
Check Mark

Answer to Problem 6.39P

The missing curved arrow notation for the proton transfer reaction and relevant electrons is shown as

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  7

Explanation of Solution

The given proton transfer reaction is

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  8

In the above reaction, the bond (O-H) is formed between the O of the second reactant and the H of the first reactant. Also, the first reactant donates a proton and forms its conjugate base, so one N-H bond of the first reactant is broken. The bond breaking and bond formation involve only valence electrons, so first all valence electrons in the given two reactants should be drawn. From that, it is clearly seen which electrons are involved in the reaction, both from the reactants and from the products, as shown below:

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  9

The appropriate movement of these valence electrons is shown by using curved arrow notations. One curved arrow is to be drawn from the lone pair on O to the H on N (highlighted blue) to illustrate the formation of the O-H bond. A second curved arrow originates from the center of the N-H bond to illustrate the breaking of that bond and points to the N atom, showing that those electrons end up as a lone pair on N. Therefore, the curved arrow notation for the proton transfer reaction is as follows:

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  10

Conclusion

The curved arrow notation for the proton transfer of the given reaction is drawn on the basis of the movement of valence electrons involved in bond breaking and bond formation.

Interpretation Introduction

(c)

Interpretation:

Missing curved arrows are to be supplied for the given proton transfer reaction. The relevant electrons are to be drawn if they are not shown.

Concept introduction:

In a proton transfer reaction, a proton is transferred from a Bronsted-Lowry acid to a Bronsted-Lowry base in a single elementary step in which one bond is broken and another is formed simultaneously. The curved arrow notation shows the movement of valence electrons, not atoms. The movement of two electrons is shown be using a double-barbed arrow. To represent bond breaking, the tail of the arrow originates from the center of a bond whereas to represent bond formation, the head of arrow points to an atom which forms the new bond, that is, ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  11bond or the region where the bond is formed if the new bond is a ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  12bond.

Expert Solution
Check Mark

Answer to Problem 6.39P

The missing curved arrow notation for the proton transfer reaction and relevant electrons is shown as

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  13

Explanation of Solution

The given proton transfer reaction is

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  14

In the above reaction, the bond (N-H) is formed between the N of the second reactant and the H of the first reactant. Also, the first reactant donates a proton and forms its conjugate base, so one C-H bond of the methyl group of the first reactant is broken. The bond breaking and bond formation involve only valence electrons, so first all valence electrons in the given two reactants should be drawn. From that, it is clearly seen which electrons are involved in the reaction, both from the reactants and from the products, as shown below:

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  15

The appropriate movement of these valence electrons is shown by using curved arrow notations. One curved arrow is to be drawn from the lone pair on N to the H on C (highlighted blue) to illustrate the formation of the N-H bond. A second curved arrow originates from the center of the C-H bond to illustrate the breaking of that bond and points to the C atom, showing that those electrons end up as a lone pair on C. Therefore, the curved arrow notation for the proton transfer reaction is as follows:

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  16

Conclusion

The curved arrow notation for the proton transfer of the given reaction is drawn on the basis of the movement of valence electrons involved in bond breaking and bond formation.

Interpretation Introduction

(d)

Interpretation:

Missing curved arrows are to be supplied for the given proton transfer reaction. The relevant electrons are to be drawn if they are not shown.

Concept introduction:

In a proton transfer reaction, a proton is transferred from a Bronsted-Lowry acid to a Bronsted-Lowry base in a single elementary step in which one bond is broken and another is formed simultaneously. The curved arrow notation shows the movement of valence electrons, not atoms. The movement of two electrons is shown be using a double-barbed arrow. To represent bond breaking, the tail of the arrow originates from the center of a bond whereas to represent bond formation, the head of arrow points to an atom which forms the new bond, that is, ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  17bond or the region where the bond is formed if the new bond is a ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  18bond.

Expert Solution
Check Mark

Answer to Problem 6.39P

The missing curved arrow notation for the proton transfer reaction and relevant electrons is shown as

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  19

Explanation of Solution

The given proton transfer reaction is

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  20

In the above reaction, the bond (O-H) is formed between the O of the first reactant and the H of the H3O+ ion. Also, H3O+ donates a proton and forms its conjugate base as H2O, so one O-H bond of H3O+ is broken. The bond breaking and bond formation involve only valence electrons, so first, all valence electrons in the given two reactants should be drawn. From that, it is clearly seen which electrons are involved in the reaction, both from the reactants and from the products, as shown below,

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  21

The appropriate movement of these valence electrons is shown by using curved arrow notations. One curved arrow is to be drawn from the lone pair on O to the H of H3O+ ion (highlighted blue) to illustrate the formation of the O-H bond. A second curved arrow originates from the center of the O-H bond to illustrate the breaking of that bond and points to the O atom, showing that those electrons end up as a lone pair on O. Therefore, the curved arrow notation for the proton transfer reaction is as follows:

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS, Chapter 6, Problem 6.39P , additional homework tip  22

Conclusion

The curved arrow notation for the proton transfer of the given reaction is drawn on the basis of the movement of valence electrons involved in bond breaking and bond formation.

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Students have asked these similar questions
I understand where the proton transfer occurs but not what the products will look like. Can you draw curved arrows to show proton transfer and what the reaction products would look like? And explain which side is favored and why
Follow the format of solving the problem where you should write the GIVEN, ASKED, SOLUTION, and ANSWER. Add curved arrows to the following reactions to indicate the flow of electrons for all of the bond-forming and bond-breaking steps.
Draw a picture of a proton transfer reaction including curved arrows

Chapter 6 Solutions

ORGANIC CHEMISTRY:PRIN...(PB)-W/ACCESS

Ch. 6 - Prob. 6.11PCh. 6 - Prob. 6.12PCh. 6 - Prob. 6.13PCh. 6 - Prob. 6.14PCh. 6 - Prob. 6.15PCh. 6 - Prob. 6.16PCh. 6 - Prob. 6.17PCh. 6 - Prob. 6.18PCh. 6 - Prob. 6.19PCh. 6 - Prob. 6.20PCh. 6 - Prob. 6.21PCh. 6 - Prob. 6.22PCh. 6 - Prob. 6.23PCh. 6 - Prob. 6.24PCh. 6 - Prob. 6.25PCh. 6 - Prob. 6.26PCh. 6 - Prob. 6.27PCh. 6 - Prob. 6.28PCh. 6 - Prob. 6.29PCh. 6 - Prob. 6.30PCh. 6 - Prob. 6.31PCh. 6 - Prob. 6.32PCh. 6 - Prob. 6.33PCh. 6 - Prob. 6.34PCh. 6 - Prob. 6.35PCh. 6 - Prob. 6.36PCh. 6 - Prob. 6.37PCh. 6 - Prob. 6.38PCh. 6 - Prob. 6.39PCh. 6 - Prob. 6.40PCh. 6 - Prob. 6.41PCh. 6 - Prob. 6.42PCh. 6 - Prob. 6.43PCh. 6 - Prob. 6.44PCh. 6 - Prob. 6.45PCh. 6 - Prob. 6.46PCh. 6 - Prob. 6.47PCh. 6 - Prob. 6.48PCh. 6 - Prob. 6.49PCh. 6 - Prob. 6.50PCh. 6 - Prob. 6.51PCh. 6 - Prob. 6.52PCh. 6 - Prob. 6.53PCh. 6 - Prob. 6.54PCh. 6 - Prob. 6.55PCh. 6 - Prob. 6.56PCh. 6 - Prob. 6.57PCh. 6 - Prob. 6.58PCh. 6 - Prob. 6.59PCh. 6 - Prob. 6.60PCh. 6 - Prob. 6.61PCh. 6 - Prob. 6.62PCh. 6 - Prob. 6.63PCh. 6 - Prob. 6.64PCh. 6 - Prob. 6.65PCh. 6 - Prob. 6.66PCh. 6 - Prob. 6.67PCh. 6 - Prob. 6.68PCh. 6 - Prob. 6.69PCh. 6 - Prob. 6.70PCh. 6 - Prob. 6.71PCh. 6 - Prob. 6.72PCh. 6 - Prob. 6.73PCh. 6 - Prob. 6.74PCh. 6 - Prob. 6.75PCh. 6 - Prob. 6.76PCh. 6 - Prob. 6.77PCh. 6 - Prob. 6.78PCh. 6 - Prob. 6.79PCh. 6 - Prob. 6.80PCh. 6 - Prob. 6.81PCh. 6 - Prob. 6.82PCh. 6 - Prob. 6.83PCh. 6 - Prob. 6.84PCh. 6 - Prob. 6.85PCh. 6 - Prob. 6.86PCh. 6 - Prob. 6.87PCh. 6 - Prob. 6.88PCh. 6 - Prob. 6.1YTCh. 6 - Prob. 6.2YTCh. 6 - Prob. 6.3YTCh. 6 - Prob. 6.4YTCh. 6 - Prob. 6.5YTCh. 6 - Prob. 6.6YTCh. 6 - Prob. 6.7YTCh. 6 - Prob. 6.8YTCh. 6 - Prob. 6.9YTCh. 6 - Prob. 6.10YTCh. 6 - Prob. 6.11YTCh. 6 - Prob. 6.12YTCh. 6 - Prob. 6.13YTCh. 6 - Prob. 6.14YTCh. 6 - Prob. 6.15YTCh. 6 - Prob. 6.16YTCh. 6 - Prob. 6.17YTCh. 6 - Prob. 6.18YTCh. 6 - Prob. 6.19YTCh. 6 - Prob. 6.20YT
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