Organic Chemistry, Ebook And Single-course Homework Access
Organic Chemistry, Ebook And Single-course Homework Access
6th Edition
ISBN: 9781319085841
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 10, Problem 10.46AP
Interpretation Introduction

(a)

Interpretation:

The increasing order of acidity of the alcohols is to be stated.

Concept introduction:

Acidity of a molecule is dependent on the value of pKa. This pKa value is known as the dissociation constant of an acid. The dissociation constant of an acid changes with the change in temperature. More is the value of pKa, lesser is the acidity of an acid. Strength of an acid also depends upon the stability of the anion generated after loosing a hydrogen ion.

Expert Solution
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Answer to Problem 10.46AP

The increasing order of acidity of the alcohols is given below.

Organic Chemistry, Ebook And Single-course Homework Access, Chapter 10, Problem 10.46AP , additional homework tip  1

Explanation of Solution

Acidity of the molecules is dependent upon the stability of the ion formed after releasing hydrogen ion.

Sulfur atom present in 1- propanethiol is larger than the size of the oxygen atom. Therefore, negative charge present on sulfur atom is stabilized. Due to this 1- propanethiol is the strongest acid among the given molecules. Tertiary alcohols are more acidic than the secondary and primary alcohols. Therefore, tertbutyl alcohol is the stronger acid than isopropyl alcohol and propyl alcohol.

Order of the acidity is shown below in Figure 1.

Organic Chemistry, Ebook And Single-course Homework Access, Chapter 10, Problem 10.46AP , additional homework tip  2

Figure 1

Conclusion

The increasing order of acidity of the molecules is propyl alcohol<isopropyl alcohol<tertbutyl alcohol<propanethiol.

Interpretation Introduction

(b)

Interpretation:

The increasing order of acidity of the molecules is to be stated.

Concept introduction:

Acidity of a molecule is dependent on the value of pKa. This pKa value is known as the dissociation constant of an acid. The dissociation constant of an acid changes with the change in temperature. More is the value of pKa, lesser is the acidity of an acid. Strength of an acid also depends upon the stability of the anion generated after loosing a hydrogen ion.

Expert Solution
Check Mark

Answer to Problem 10.46AP

The increasing order of acidity of the molecules is given below.

Organic Chemistry, Ebook And Single-course Homework Access, Chapter 10, Problem 10.46AP , additional homework tip  3

Explanation of Solution

Acidity of the molecules is dependent upon the stability of the ion formed after releasing hydrogen ion. Sulfur atom present in 3- chloro -1- propanethiol is larger than the size of the oxygen atom. Therefore, negative charge present on sulfur atom is stabilized. Due to this, 3- chloro -1- propanethiol is the strongest acid among the given molecules. Position of the electronegative atom also determines the strength of an acid. Closer the electronegative atom to the negative charge generated after releasing the hydrogen ion, more is the strength of the acid.

Therefore, increasing order of the given molecules is shown below in Figure 2.

Organic Chemistry, Ebook And Single-course Homework Access, Chapter 10, Problem 10.46AP , additional homework tip  4

Figure 2

Conclusion

The increasing order of acidity of the given molecules is 2-chloroethanol<3-chloro-1-propanethiol<2-chloro- 1-propanethiol.

Interpretation Introduction

(c)

Interpretation:

The increasing order of acidity of the molecules is to be stated.

Concept introduction:

Acidity of a molecule is dependent on the value of pKa. This pKa value is known as the dissociation constant of an acid. The dissociation constant of an acid changes with the change in temperature. More is the value of pKa, lesser is the acidity of an acid. Strength of an acid also depends upon the stability of the anion generated after loosing a hydrogen ion.

Expert Solution
Check Mark

Answer to Problem 10.46AP

The increasing order of acidity of the molecules is stated below.

CH3N¨HCH2CH2CH2O¨¨H<CH3N¨HCH2CH2O¨¨H<(CH3)3N+CH2CH2O¨¨H

Explanation of Solution

Acidity of the molecules is dependent upon the stability of the ion formed after releasing hydrogen ion. Nitrogen atom which is positively charged, stabilizes the negative charge which is generated after releasing the hydrogen ion. Therefore, structure 3 is the most stable structure with most acidic character. Position of the electronegative atom also determines the strength of an acid. Closer the electronegative atom to the generated negative charge after releasing the hydrogen ion, more is the strength of the acid.

Therefore, increasing order of the given molecules is stated below.

CH3N¨HCH2CH2CH2O¨¨H<CH3N¨HCH2CH2O¨¨H<(CH3)3N+CH2CH2O¨¨H

Conclusion

The increasing order of acidity of the given molecules is CH3N¨HCH2CH2CH2O¨¨H<CH3N¨HCH2CH2O¨¨H<(CH3)3N+CH2CH2O¨¨H.

Interpretation Introduction

(d)

Interpretation:

The increasing order of acidity of the molecules is to be stated.

Concept introduction:

Acidity of a molecule is dependent on the value of pKa. This pKa value is known as the dissociation constant of an acid. The dissociation constant of an acid changes with the change in temperature. More is the value of pKa, lesser is the acidity of an acid. Strength of an acid also depends upon the stability of the anion generated after loosing a hydrogen ion.

Expert Solution
Check Mark

Answer to Problem 10.46AP

The increasing order of acidity of the molecules is stated below.

: O ¨¨CH2CH2O¨¨H<CH3CH2CH2O¨¨H<CH3 O ¨¨CH2CH2O¨¨H<CH3 O ¨¨CH2CH2CH2O ¨+H

Explanation of Solution

Acidity of the molecules is dependent upon the stability of the ion formed after releasing the hydrogen ion. In structure 4, a neutral species is generated after releasing the H+ ion. Therefore, the molecule in structure 4 is the most acidic in nature. Position of the electronegative atom also determines the strength of an acid. Closer the electronegative atom to the generated negative charge after releasing the hydrogen ion, more is the strength of an acid. Therefore, molecule 3 is less acidic than molecule in structure 4. In structure 1, oxygen has already a negative charge. Therefore, it is already in its stabilized form and acts as a weakest acid among the given molecules.

Therefore, increasing order of acidity of the given molecules is stated below.

: O ¨¨CH2CH2O¨¨H<CH3CH2CH2O¨¨H<CH3 O ¨¨CH2CH2O¨¨H<CH3 O ¨¨CH2CH2CH2 O ¨+H

Conclusion

The increasing order of acidity of the given molecules is : O ¨¨CH2CH2O¨¨H<CH3CH2CH2O¨¨H<CH3 O ¨¨CH2CH2O¨¨H<CH3 O ¨¨CH2CH2CH2 O ¨+H

Interpretation Introduction

(e)

Interpretation:

The increasing order of acidity of the molecules is to be stated.

Concept introduction:

Acidity of a molecule is dependent on the value of pKa. This pKa value is known as the dissociation constant of an acid. The dissociation constant of an acid changes with the change in temperature. More is the value of pKa, lesser is the acidity of an acid. Strength of an acid also depends upon the stability of the anion generated after loosing a hydrogen ion.

Expert Solution
Check Mark

Answer to Problem 10.46AP

The increasing order of acidity of the molecules is stated below.

Organic Chemistry, Ebook And Single-course Homework Access, Chapter 10, Problem 10.46AP , additional homework tip  5

Explanation of Solution

Acidity of the molecules is dependent upon the stability of the ion formed after releasing the hydrogen ion. In structure 3, Size of the sulfur atom is more as compared to the size of the oxygen atom. The H+ ion is held loosely with the sulfur atom. Therefore, the molecule in structure 3 easily releases the hydrogen ion and becomes the most acidic in nature. In structure 2 and 3, a neutral species is generated after releasing the H+ ion Therefore, molecule 2 and 3 are more acidic than molecule 1.

Therefore, increasing order of the given molecules is stated below in Figure 3.

Organic Chemistry, Ebook And Single-course Homework Access, Chapter 10, Problem 10.46AP , additional homework tip  6

Figure 3

Conclusion

The increasing order of acidity of the given molecules is shown above in Figure 3.

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Using pKa Values to Determine Relative Acidity and Basicity Rank the following compounds in order of increasing acidity, and then rank their conjugate bases in order of increasing basicity.
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