OWLv2 with MindTap Reader, 1 term (6 months) Printed Access Card for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition
OWLv2 with MindTap Reader, 1 term (6 months) Printed Access Card for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition
8th Edition
ISBN: 9781305582439
Author: Brown, William H.; Iverson, Brent L.; Anslyn, Eric; Foote, Christopher S.
Publisher: Cengage Learning
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Chapter 4, Problem 4.38AP

(a)

Interpretation Introduction

Interpretation:

The most acidic hydrogen in given molecule has to be labelled and justify it using pKa values of it.

Concept Introduction:

Position of equilibrium in acid-base reaction:

In an acid-base reaction, the position of equilibrium always favors reaction of the stronger acid and stronger base to form the weaker acid and weaker base. Therefore, the major species present at equilibrium in an acid-base reaction are weaker acid and weaker base.  The reaction equilibrium shifts to a direction where weaker acid and weaker base is formed.  Acids with greater pKa values are weak acids and base with greater pKb values are weaker base.

(a)

Expert Solution
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Explanation of Solution

Given molecule,

    HOCH2CH2NH2

Increase in pKa value decreases Ka value, which determines acidity of a compound.  Therefore, hydrogen with lower pKa value has higher Ka value and more acidic.  In given compound, hydrogen attached to oxygen has less pKa value than hydrogen bonded to nitrogen.  The most acidic hydrogen atom is labelled as,

     HOCH2CH2NH2pKa ~16 ~38

(b)

Interpretation Introduction

Interpretation:

The most acidic hydrogen in given molecule has to be labelled and justify it using pKa values of it.

Concept Introduction:

Position of equilibrium in acid-base reaction:

In an acid-base reaction, the position of equilibrium always favors reaction of the stronger acid and stronger base to form the weaker acid and weaker base. Therefore, the major species present at equilibrium in an acid-base reaction are weaker acid and weaker base.  The reaction equilibrium shifts to a direction where weaker acid and weaker base is formed.  Acids with greater pKa values are weak acids and base with greater pKb values are weaker base.

(b)

Expert Solution
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Explanation of Solution

Given molecule,

    HSCH2CH2NH2

Increase in pKa value decreases Ka value, which determines acidity of a compound.  Therefore, hydrogen with lower pKa value has higher Ka value and more acidic.  In given compound, hydrogen attached to sulfur has less pKa value than hydrogen bonded to nitrogen.  The most acidic hydrogen atom is labelled as,

     HSCH2CH2NH2pKa ~7 ~38

(c)

Interpretation Introduction

Interpretation:

The most acidic hydrogen in given molecule has to be labelled and justify it using pKa values of it.

Concept Introduction:

Position of equilibrium in acid-base reaction:

In an acid-base reaction, the position of equilibrium always favors reaction of the stronger acid and stronger base to form the weaker acid and weaker base. Therefore, the major species present at equilibrium in an acid-base reaction are weaker acid and weaker base.  The reaction equilibrium shifts to a direction where weaker acid and weaker base is formed.  Acids with greater pKa values are weak acids and base with greater pKb values are weaker base.

(c)

Expert Solution
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Explanation of Solution

Given molecule,

    HOCH2CH2CCH

Increase in pKa value decreases Ka value, which determines acidity of a compound.  Therefore, hydrogen with lower pKa value has higher Ka value and more acidic.  In given compound, hydrogen attached to oxygen has less pKa value than hydrogen bonded to terminal carbon.  The most acidic hydrogen atom is labelled as,

     HOCH2CH2CCHpKa ~16 ~25

(d)

Interpretation Introduction

Interpretation:

The most acidic hydrogen in given molecule has to be labelled and justify it using pKa values of it.

Concept Introduction:

Position of equilibrium in acid-base reaction:

In an acid-base reaction, the position of equilibrium always favors reaction of the stronger acid and stronger base to form the weaker acid and weaker base. Therefore, the major species present at equilibrium in an acid-base reaction are weaker acid and weaker base.  The reaction equilibrium shifts to a direction where weaker acid and weaker base is formed.  Acids with greater pKa values are weak acids and base with greater pKb values are weaker base.

(d)

Expert Solution
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Explanation of Solution

Given molecule,

    HOCOCH2CH2SH

Increase in pKa value decreases Ka value, which determines acidity of a compound.  Therefore, hydrogen with lower pKa value has higher Ka value and more acidic.  In given compound, hydrogen attached to oxygen has less pKa value than hydrogen bonded to sulfur.  The most acidic hydrogen atom is labelled as,

     HOCOCH2CH2SHpKa ~4.5 ~7

(e)

Interpretation Introduction

Interpretation:

The most acidic hydrogen in given molecule has to be labelled and justify it using pKa values of it.

Concept Introduction:

Position of equilibrium in acid-base reaction:

In an acid-base reaction, the position of equilibrium always favors reaction of the stronger acid and stronger base to form the weaker acid and weaker base. Therefore, the major species present at equilibrium in an acid-base reaction are weaker acid and weaker base.  The reaction equilibrium shifts to a direction where weaker acid and weaker base is formed.  Acids with greater pKa values are weak acids and base with greater pKb values are weaker base.

(e)

Expert Solution
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Explanation of Solution

Given molecule,

    OWLv2 with MindTap Reader, 1 term (6 months) Printed Access Card for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition, Chapter 4, Problem 4.38AP , additional homework tip  1

Increase in pKa value decreases Ka value, which determines acidity of a compound.  Therefore, hydrogen with lower pKa value has higher Ka value and more acidic.  In given compound, hydrogen attached to carboxylic acid oxygen has less pKa value than hydrogen bonded to oxygen of alcohol.  The most acidic hydrogen atom is labelled as,

    OWLv2 with MindTap Reader, 1 term (6 months) Printed Access Card for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition, Chapter 4, Problem 4.38AP , additional homework tip  2

(f)

Interpretation Introduction

Interpretation:

The most acidic hydrogen in given molecule has to be labelled and justify it using pKa values of it.

Concept Introduction:

Position of equilibrium in acid-base reaction:

In an acid-base reaction, the position of equilibrium always favors reaction of the stronger acid and stronger base to form the weaker acid and weaker base. Therefore, the major species present at equilibrium in an acid-base reaction are weaker acid and weaker base.  The reaction equilibrium shifts to a direction where weaker acid and weaker base is formed.  Acids with greater pKa values are weak acids and base with greater pKb values are weaker base.

(f)

Expert Solution
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Explanation of Solution

Given molecule,

    H3N+CH2CH2COOH

Increase in pKa value decreases Ka value, which determines acidity of a compound.  Therefore, hydrogen with lower pKa value has higher Ka value and more acidic.  In given compound, hydrogen attached to oxygen has less pKa value than hydrogen bonded to nitrogen.  The most acidic hydrogen atom is labelled as,

     H3N+CH2CH2COOHpKa ~9 ~4.5

(g)

Interpretation Introduction

Interpretation:

The most acidic hydrogen in given molecule has to be labelled and justify it using pKa values of it.

Concept Introduction:

Position of equilibrium in acid-base reaction:

In an acid-base reaction, the position of equilibrium always favors reaction of the stronger acid and stronger base to form the weaker acid and weaker base. Therefore, the major species present at equilibrium in an acid-base reaction are weaker acid and weaker base.  The reaction equilibrium shifts to a direction where weaker acid and weaker base is formed.  Acids with greater pKa values are weak acids and base with greater pKb values are weaker base.

(g)

Expert Solution
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Explanation of Solution

Given molecule,

    H3N+CH2CH2COO-

Increase in pKa value decreases Ka value, which determines acidity of a compound.  Therefore, hydrogen with lower pKa value has higher Ka value and more acidic.  In given compound, hydrogen attached to nitrogen is the only acidic hydrogen and labelled as,

     H3N+CH2CH2COO-pKa ~9

(h)

Interpretation Introduction

Interpretation:

The most acidic hydrogen in given molecule has to be labelled and justify it using pKa values of it.

Concept Introduction:

Position of equilibrium in acid-base reaction:

In an acid-base reaction, the position of equilibrium always favors reaction of the stronger acid and stronger base to form the weaker acid and weaker base. Therefore, the major species present at equilibrium in an acid-base reaction are weaker acid and weaker base.  The reaction equilibrium shifts to a direction where weaker acid and weaker base is formed.  Acids with greater pKa values are weak acids and base with greater pKb values are weaker base.

(h)

Expert Solution
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Explanation of Solution

Given molecule,

    HSCH2CH2OH

Increase in pKa value decreases Ka value, which determines acidity of a compound.  Therefore, hydrogen with lower pKa value has higher Ka value and more acidic.  In given compound, hydrogen attached to sulfur has less pKa value than hydrogen bonded to oxygen.  The most acidic hydrogen atom is labelled as,

     HSCH2CH2OHpKa ~7 ~16

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Chapter 4 Solutions

OWLv2 with MindTap Reader, 1 term (6 months) Printed Access Card for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition

Ch. 4 - For each conjugate acid-base pair, identify the...Ch. 4 - Complete a net ionic equation for each...Ch. 4 - Arrange the compounds in each set in order of...Ch. 4 - Prob. 4.12PCh. 4 - In acetic acid, CH3COOH, the OH hydrogen is more...Ch. 4 - Which has the larger numerical value? (a) The pKa...Ch. 4 - In each pair, select the stronger acid. (a)...Ch. 4 - Arrange the compounds in each set in order of...Ch. 4 - Arrange the compounds in each set in order of...Ch. 4 - If the G for a reaction is 4.5 kcal/mol at 298 K,...Ch. 4 - Calculate the Keq for the following reactions from...Ch. 4 - Prob. 4.20PCh. 4 - Answer true or false to the following statements...Ch. 4 - In each of the following three reaction coordinate...Ch. 4 - The acid-base chemistry reaction of barium...Ch. 4 - Unless under pressure, carbonic acid (H2CO3) in...Ch. 4 - Prob. 4.25PCh. 4 - Acetic acid, CH3COOH, is a weak organic acid, pKa...Ch. 4 - Benzoic acid, C6H5COOH (pKa 4.19), is only...Ch. 4 - Prob. 4.28PCh. 4 - One way to determine the predominant species at...Ch. 4 - Will acetylene react with sodium hydride according...Ch. 4 - Prob. 4.31PCh. 4 - For each equation, label the Lewis acid and the...Ch. 4 - Complete the equation for the reaction between...Ch. 4 - Each of these reactions can be written as a Lewis...Ch. 4 - The sec-butyl cation can react as both a...Ch. 4 - Prob. 4.36APCh. 4 - Prob. 4.37APCh. 4 - Prob. 4.38APCh. 4 - Explain why the hydronium ion, H3O+, is the...Ch. 4 - What is the strongest base that can exist in...Ch. 4 - Prob. 4.42APCh. 4 - Prob. 4.43APCh. 4 - Methyl isocyanate, CH3N=C=O, is used in the...Ch. 4 - Offer an explanation for the following...Ch. 4 - Prob. 4.46APCh. 4 - Alcohols (Chapter 10) are weak organic acids, pKa...Ch. 4 - As we shall see in Chapter 19, hydrogens on a...Ch. 4 - 2,4-Pentanedione is a considerably stronger acid...Ch. 4 - Write an equation for the acid-base reaction...Ch. 4 - Prob. 4.51APCh. 4 - Prob. 4.52APCh. 4 - Prob. 4.53APCh. 4 - Following is a structural formula for imidazole, a...
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