Organic Chemistry - With Access (Custom)
Organic Chemistry - With Access (Custom)
4th Edition
ISBN: 9781259147760
Author: OHIO UNIV.
Publisher: MCG
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Chapter 2, Problem 2.49P

Rank the following compounds in order of increasing acidity.

a. NH 3 , H 2 O , HF e. CH 3 OH , CH 3 NH 2 , CH 3 CH 3

b. HBr , HCl , HF f. HCl , H 2 O , H 2 S

c. H 2 O , H 3 O + , HO g. CH 3 CH 2 CH 3 , ClCH 2 CH 2 OH , CH 3 CH 2 OH

d. NH 3 , H 2 O , H 2 S h. HC CCH 2 CH 3 , CH 3 CH 2 CH 2 CH 3 , CH 3 CH = CHCH 3

Expert Solution
Check Mark
Interpretation Introduction

(a)

Interpretation: The order of increasing acidity for the given compounds is to be stated.

Concept introduction: In a simple molecule, the acidity of a particular proton depends on the atom to which that proton is attached.

In the periodic table, the acidity of a compound increases across a row as the electronegativity increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom. The order of acidity is CH < NH < OH < FH.

Answer to Problem 2.49P

The correct order of increasing acidity is NH3<H2O<HF.

Explanation of Solution

The given compounds are NH3, H2O and HF.

The given compounds contain OH, NH and FH bonds. The acidity of HA increases across a row as the electronegativity of A increases on moving from left to right in a periodic table. Hence, the correct order of increasing acidity is NH3<H2O<HF.

Conclusion

The correct order of increasing acidity is NH3<H2O<HF.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The order of increasing acidity for the given compounds is to be stated.

Concept introduction: In a simple molecule, the acidity of a particular proton depends on the atom to which that proton is attached.

In the periodic table, the acidity of a compound increases across a row as the electronegativity increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom.

Answer to Problem 2.49P

The correct order of increasing acidity is

Explanation of Solution

The given compounds are HBr, HCl and HF.

The given compounds contain BrH, ClH and FH bonds. The acidity of a compound increases across a row as the electronegativity increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom. Hence, the correct order of increasing acidity is HBr<HCl<HF.

Conclusion

The correct order of increasing acidity is HBr<HCl<HF.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation: The order of increasing acidity for the given compounds is to be stated.

Concept introduction: In a simple molecule, the acidity of a particular proton depends on the atom to which that proton is attached.

Answer to Problem 2.49P

The correct order of increasing acidity is HO<H2O<H3O+.

Explanation of Solution

The given compounds are H2O, H3O+, and HO.

Hydronium ion (H3O+) ionizes to water and a proton, water ionizes to hydroxide and a proton and hydroxide ionizes to form oxide and a proton. The conjugate base formed in case of hydronium is more stable than the conjugate base formed in water and hydroxide. The tendency of hydronium ion to donate its proton is higher than that of water and hydroxide.

Hence, the correct order of increasing acidity is HO<H2O<H3O+.

Conclusion

The correct order of increasing acidity is HO<H2O<H3O+.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation: The order of increasing acidity for the given compounds is to be stated.

Concept introduction: In a simple molecule, the acidity of a particular proton depends on the atom to which that proton is attached.

In the periodic table, the acidity of a compound increases across a row as the electronegativity increases on moving from left to right and down a column as the size of atom increases on moving from top to bottom.

Answer to Problem 2.49P

The correct order of increasing acidity is NH3<H2O<H2S.

Explanation of Solution

The given compounds are NH3, H2O, and H2S.

The given compounds contain OH, NH and SH bonds. The acidity of HA increases across a row as the electronegativity of A increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom in a periodic table. Hence, the correct order of increasing acidity is NH3<H2O<H2S.

Conclusion

The correct order of increasing acidity is NH3<H2O<H2S.

Expert Solution
Check Mark
Interpretation Introduction

(e)

Interpretation: The order of increasing acidity for the given compounds is to be stated.

Concept introduction: In a simple molecule, the acidity of a particular proton depends on the atom to which that proton is attached.

In the periodic table, the acidity of a compound increases across a row as the electronegativity increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom. The order of acidity is CH < NH < OH < FH.

Answer to Problem 2.49P

The correct order of increasing acidity is CH3CH3<CH3NH2<CH3OH.

Explanation of Solution

The given compounds are CH3CH3, CH3NH2, and CH3OH.

The given compounds contain CH, OH and NH bonds. The acidity of HA increases across a row as the electronegativity of A increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom in a periodic table. Hence, the correct order of increasing acidity is CH3CH3<CH3NH2<CH3OH.

Conclusion

The correct order of increasing acidity is CH3CH3<CH3NH2<CH3OH.

Expert Solution
Check Mark
Interpretation Introduction

(f)

Interpretation: The order of increasing acidity for the given compounds is to be stated.

Concept introduction: In a simple molecule, the acidity of a particular proton depends on the atom to which that proton is attached.

In the periodic table, the acidity of a compound increases across a row as the electronegativity increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom.

Answer to Problem 2.49P

The correct order of increasing acidity is H2O<H2S<HCl.

Explanation of Solution

The given compounds are H2O, H2S and HCl.

The given compounds contain OH, SH and ClH bonds. The acidity of HA increases across a row as the electronegativity of A increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom in a periodic table. Hence, the correct order of increasing acidity is H2O<H2S<HCl.

Conclusion

The correct order of increasing acidity is H2O<H2S<HCl.

Expert Solution
Check Mark
Interpretation Introduction

(g)

Interpretation: The order of increasing acidity for the given compounds is to be stated.

Concept introduction: In a simple molecule, the acidity of a particular proton depends on the atom to which that proton is attached.

In the periodic table, the acidity of a compound increases across a row as the electronegativity increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom.

Answer to Problem 2.49P

The correct order of increasing acidity is CH3CH2CH3<CH3CH2OH<ClCH2CH2OH.

Explanation of Solution

The given compounds are CH3CH2CH3, CH3CH2OH and ClCH2CH2OH.

The given compounds contain CH, and OH bonds. The acidity of HA increases across a row as the electronegativity of A increases on moving from left to right and decreases down a column as the size of atom increases on moving from top to bottom in a periodic table. The acidity of the compound increases due to the presence of negative inductive effect of chloro group. Hence, the correct order of increasing acidity is CH3CH2CH3<CH3CH2OH<ClCH2CH2OH.

Conclusion

The correct order of increasing acidity is CH3CH2CH3<CH3CH2OH<ClCH2CH2OH.

Expert Solution
Check Mark
Interpretation Introduction

(h)

Interpretation: The order of increasing acidity for the given compounds is to be stated.

Concept introduction: In hydrocarbons, alkanes, alkenes and alkynes, the order of acidity is predicted by their s-character. More is the s-character, more is the acidity.

Answer to Problem 2.49P

The correct order of increasing acidity is,

Organic Chemistry - With Access (Custom), Chapter 2, Problem 2.49P , additional homework tip  1

Explanation of Solution

The given compounds are,

Organic Chemistry - With Access (Custom), Chapter 2, Problem 2.49P , additional homework tip  2

Figure 1

For alkanes, alkenes and alkynes, the order of s-character is,

Alkyne>Alkene>Alkane

More is the s-character of a compound, more is the acidity. Hence, the correct order of increasing acidity is shown below.

Organic Chemistry - With Access (Custom), Chapter 2, Problem 2.49P , additional homework tip  3

Figure 2

Conclusion

The correct order of increasing acidity is shown in Figure 2.

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Chapter 2 Solutions

Organic Chemistry - With Access (Custom)

Ch. 2 - Draw the products of each reaction and determine...Ch. 2 - Prob. 2.12PCh. 2 - Without reference to a pKa table, decide which...Ch. 2 - which compound in each pair of isomers is the...Ch. 2 - Prob. 2.15PCh. 2 - Which hydrogen in pseudoephedrine, the nasal...Ch. 2 - whichcompound in each pair is the stronger acid? a...Ch. 2 - Glycolic acid, HOCH2CO2H, is the simplest member...Ch. 2 - Explain the apparent paradox. HBr is a stronger...Ch. 2 - The CH bond in acetone, (CH3)2C=O, has a pKa of...Ch. 2 - Acetonitrile (CH3CN) has a pKa of 25, making it...Ch. 2 - For each pair of compounds: [1] Which indicated H...Ch. 2 - Rank the compounds in each group in order of...Ch. 2 - Which proton in each of the following drugs is...Ch. 2 - Prob. 2.25PCh. 2 - Problem 2.29 Compounds like amphetamine that...Ch. 2 - Problem 2.30 Which species are Lewis bases? a. b....Ch. 2 - Which species are Lewis acids? a. b. c. d. Ch. 2 - For each reaction, label the Lewis acid and base....Ch. 2 - Prob. 2.30PCh. 2 - Prob. 2.31PCh. 2 - Prob. 2.32PCh. 2 - 2.36 Propranolol is an antihypertensive agent—that...Ch. 2 - 2.37 Amphetamine is a powerful stimulant of the...Ch. 2 - Prob. 2.35PCh. 2 - Prob. 2.36PCh. 2 - a Draw the conjugate acid of ethylene, CH2 = CH2....Ch. 2 - 2.40 Draw the products formed from the acid-base...Ch. 2 - Draw the products formed from the acid-base...Ch. 2 - Prob. 2.40PCh. 2 - Draw the product of acid-base reaction. a. c. b....Ch. 2 - Prob. 2.42PCh. 2 - Prob. 2.43PCh. 2 - What is Ka for each compound? Use a calculator...Ch. 2 - What is the pKa for each compound? a. b. c.Ch. 2 - Which of the following bases are strong enough to...Ch. 2 - Which compounds can be deprotonated by OH, so that...Ch. 2 - Draw the product of each reaction. Use the pKa...Ch. 2 - Rank the following compounds in order of...Ch. 2 - Rank the following ions in order of increasing...Ch. 2 - Prob. 2.51PCh. 2 - Prob. 2.52PCh. 2 - The pKa of three CH bonds is given below. a. For...Ch. 2 - a. What is the conjugate acid of A? b. What is the...Ch. 2 - 2.56 Draw the structure of a constitutional isomer...Ch. 2 - 2.57 Many drugs are Bronsted-Lowry acids or...Ch. 2 - Dimethyl ether (CH3OCH3) and ethanol (CH3CH2OH)...Ch. 2 - Prob. 2.58PCh. 2 - Ethyl butanoate, CH3CH2CH2CO2CH2CH3, is one of the...Ch. 2 - Prob. 2.60PCh. 2 - 2.61 Label the three most acidic hydrogen atoms in...Ch. 2 - Prob. 2.62PCh. 2 - 2.64 Classify each species as a Lewis acid, a...Ch. 2 - Prob. 2.64PCh. 2 - Draw the products of each Lewis acid-base...Ch. 2 - Prob. 2.66PCh. 2 - Prob. 2.67PCh. 2 - 2.70 Hydroxide can react as a Brønsted-Lowry base...Ch. 2 - 2.71 Answer the following questions about esmolol,...Ch. 2 - Prob. 2.70PCh. 2 - 2.72 DBU, is a base we will encounter in...Ch. 2 - 2.73 Molecules like acetamide can be protonated...Ch. 2 - Two pKa values are reported for malonic acid, a...Ch. 2 - Prob. 2.74PCh. 2 - 2.76 Write a stepwise reaction sequence using...Ch. 2 - Prob. 2.76PCh. 2 - 2.78 Which compound, M or N, is the stronger acid?...
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