PKG ORGANIC CHEMISTRY
PKG ORGANIC CHEMISTRY
5th Edition
ISBN: 9781259963667
Author: SMITH
Publisher: MCG
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Chapter 2, Problem 2.51P

Rank the following ions in order of increasing basicity.

a. CH 3 C H 2 , CH 3 O , CH 3 N H c. Chapter 2, Problem 2.51P, 2.51 Rank the following ions in order of increasing basicity.

a. 	c. 
b. 		d. 
 , example  1

b. CH 3 , HO , Br d. Chapter 2, Problem 2.51P, 2.51 Rank the following ions in order of increasing basicity.

a. 	c. 
b. 		d. 
 , example  2

Expert Solution
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Interpretation Introduction

(a)

Interpretation: The order of increasing basicity for the given ions is to be ranked.

Concept introduction: A strong base possesses a weak conjugate acid and a strong acid has a weak conjugate base. In the periodic table, the basicity of ions decreases 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 2.51P

The increasing order of basicity for the given ions is  CH3O < CH3NH < CH3CH2.

Explanation of Solution

The given ions are CH3CH2, CH3O, CH3NH. Oxygen is more electronegative than nitrogen. The formation of more stable anion occurs by the more electronegative atom that bears a negative charge. The more stable anion are weaker bases. Therefore, in the given anions CH3O is a weaker base as compared to CH3NH. Also, the basicity of ions decreases across a row as the electronegativity increases. Hence, the increasing order of basicity for the given ions is  CH3O < CH3NH < CH3CH2.

Conclusion

The increasing order of basicity for the given ions is  CH3O < CH3NH < CH3CH2.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The order of increasing basicity for the given ions is to be ranked.

Concept introduction: A strong base possesses a weak conjugate acid and a strong acid has a weak conjugate base. In the periodic table, the basicity of ions decreases 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 2.51P

The increasing order of basicity for the given ions is Br < HO < CH3.

Explanation of Solution

The given ions are CH3, HO, Br. The basicity of ions decreases across a row as the electronegativity increases. A strong acid has a weak conjugate base. The conjugate acid of CH3 is CH4 which is a very weak acid. The conjugate acid of OH is H2O which is a weak acid and the conjugate acid of Br is HBr which is a strong acid. Therefore, Br is a weak base than OH and OH is a weak base than CH3. Hence, the increasing order of basicity for the given ions is Br < HO < CH3.

Conclusion

The increasing order of basicity for the given ions is Br < HO < CH3.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation: The order of increasing basicity for the given ions is to be ranked.

Concept introduction: A strong base possesses a weak conjugate acid and a strong acid has a weak conjugate base. In the periodic table, the basicity of ions decreases 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 2.51P

The order of increasing basicity for the given ions is ClCH2COO < CH3COO < CH3CH2O.

Explanation of Solution

The given ions are CH3COO, CH3CH2O and ClCH2COO. The ion ClCH2COO, contains chlorine atom which is an electron withdrawing group and makes the ion more acidic. Therefore, it is less basic than the other two ions.

The conjugate acid of CH3CH2O is CH3CH2OH which is an alcohol. Alcohols are weaker acids as compared to carboxylic acids. Therefore, their conjugate bases are stronger than the conjugate bases of carboxylic acids. Hence, the order of increasing basicity for the given ions is ClCH2COO < CH3COO < CH3CH2O.

Conclusion

The order of increasing basicity for the given ions is ClCH2COO < CH3COO < CH3CH2O.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation: The order of increasing basicity for the given ions is to be ranked.

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

Answer to Problem 2.51P

The order of increasing basicity for the given ions is shown in Figure 2.

Explanation of Solution

The given ions are,

PKG ORGANIC CHEMISTRY, Chapter 2, Problem 2.51P , additional homework tip  1

Figure 1

More is the s-character of a compound, less is the basicity. Alkanes contain 25% s-character, alkenes have 33% s-character and alkynes have 50% s-character. Hence, the correct order of increasing basicity is shown below.

PKG ORGANIC CHEMISTRY, Chapter 2, Problem 2.51P , additional homework tip  2

Figure 2

Conclusion

The order of increasing basicity for the given ions is shown in Figure 2.

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Chapter 2 Solutions

PKG ORGANIC CHEMISTRY

Ch. 2 - Prob. 2.11PCh. 2 - Draw the products of each reaction and determine...Ch. 2 - Prob. 2.13PCh. 2 - Without reference to a pKa table, decide which...Ch. 2 - Rank the labeled H atoms in the following compound...Ch. 2 - Which hydrogen in each molecule is most...Ch. 2 - Which hydrogen in pseudoephedrine, the nasal...Ch. 2 - Which compound in each pair of isomers is the...Ch. 2 - Which compound in each pair is the stronger acid?...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 - Which anion A or B is the stronger base? ABCh. 2 - Prob. 2.28PCh. 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. 2.33PCh. 2 - Prob. 2.34PCh. 2 - Label the Lewis acid and base. Use curved arrow...Ch. 2 - 2.36 Propranolol is an antihypertensive agent—that...Ch. 2 - 2.37 Amphetamine is a powerful stimulant of the...Ch. 2 - 2.38 What is the conjugate acid of each base? a....Ch. 2 - 2.39 What is the conjugate base of each acid? a....Ch. 2 - 2.40 Draw the products formed from the acid-base...Ch. 2 - Draw the products formed from the acid-base...Ch. 2 - Draw the products of each proton transfer...Ch. 2 - Prob. 2.43PCh. 2 - Prob. 2.44PCh. 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 products of each reaction. Use the pKa...Ch. 2 - Rank the following compounds in order of...Ch. 2 - 2.51 Rank the following ions in order of...Ch. 2 - Prob. 2.52PCh. 2 - Prob. 2.53PCh. 2 - 2.54 The of three 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 - 2.59 Atenolol is a (beta) blocker, a drug used to...Ch. 2 - 2.60 Use the principles in Section 2.5 to label...Ch. 2 - 2.61 Label the three most acidic hydrogen atoms in...Ch. 2 - Prob. 2.62PCh. 2 - 2.63 Classify each compound as a Lewis base, a...Ch. 2 - 2.64 Classify each species as a Lewis acid, a...Ch. 2 - Label the Lewis acid and Lewis base in each...Ch. 2 - 2.66 Draw the products of each Lewis acid-base...Ch. 2 - Prob. 2.67PCh. 2 - 2.68 Answer the following questions about the four...Ch. 2 - Prob. 2.69PCh. 2 - 2.70 Hydroxide can react as a Brønsted-Lowry base...Ch. 2 - 2.71 Answer the following questions about esmolol,...Ch. 2 - 2.72 DBU, is a base we will encounter in...Ch. 2 - 2.73 Molecules like acetamide can be protonated...Ch. 2 - Prob. 2.74PCh. 2 - Prob. 2.75PCh. 2 - 2.76 Write a stepwise reaction sequence using...Ch. 2 - Prob. 2.77PCh. 2 - 2.78 Which compound, M or N, is the stronger acid?...
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