Brønsted-Lowry Acids and Bases

Devin R Latimer

32 Brønsted-Lowry Acids and Bases

Learning Objectives

By the end of this section, you will be able to:

Identify acids, bases, and conjugate acid-base pairs according to the Brønsted-Lowry definition
Write equations for acid and base ionization reactions
Use the ion-product constant for water to calculate hydronium and hydroxide ion concentrations
Describe the acid-base behavior of amphiprotic substances

The acid-base reaction class has been studied for quite some time. In 1680, Robert Boyle reported traits of acid solutions that included their ability to dissolve many substances, to change the colors of certain natural dyes, and to lose these traits after coming in contact with alkali (base) solutions. In the eighteenth century, it was recognized that acids have a sour taste, react with limestone to liberate a gaseous substance (now known to be CO₂), and interact with alkalis to form neutral substances. In 1815, Humphry Davy contributed greatly to the development of the modern acid-base concept by demonstrating that hydrogen is the essential constituent of acids. Around that same time, Joseph Louis Gay-Lussac concluded that acids are substances that can neutralize bases and that these two classes of substances can be defined only in terms of each other. The significance of hydrogen was reemphasized in 1884 when Svante Arrhenius defined an acid as a compound that dissolves in water to yield hydrogen cations (now recognized to be hydronium ions) and a base as a compound that dissolves in water to yield hydroxide anions.

Johannes Brønsted and Thomas Lowry proposed a more general description in 1923 in which acids and bases were defined in terms of the transfer of hydrogen ions, H⁺. (Note that these hydrogen ions are often referred to simply as protons, since that subatomic particle is the only component of cations derived from the most abundant hydrogen isotope, ¹H.) A compound that donates a proton to another compound is called a Brønsted-Lowry acid, and a compound that accepts a proton is called a Brønsted-Lowry base. An acid-base reaction is, thus, the transfer of a proton from a donor (acid) to an acceptor (base).

The concept of conjugate pairs is useful in describing Brønsted-Lowry acid-base reactions (and other reversible reactions, as well). When an acid donates H⁺, the species that remains is called the conjugate base of the acid because it reacts as a proton acceptor in the reverse reaction. Likewise, when a base accepts H⁺, it is converted to its conjugate acid. The reaction between water and ammonia illustrates this idea. In the forward direction, water acts as an acid by donating a proton to ammonia and subsequently becoming a hydroxide ion, OH⁻, the conjugate base of water. The ammonia acts as a base in accepting this proton, becoming an ammonium ion, ${{\text{NH}}_{4}}^{\text{+}}\text{,}$ the conjugate acid of ammonia. In the reverse direction, a hydroxide ion acts as a base in accepting a proton from ammonium ion, which acts as an acid.

The reaction between a Brønsted-Lowry acid and water is called acid ionization. For example, when hydrogen fluoride dissolves in water and ionizes, protons are transferred from hydrogen fluoride molecules to water molecules, yielding hydronium ions and fluoride ions:

Base ionization of a species occurs when it accepts protons from water molecules. In the example below, pyridine molecules, C₅NH₅, undergo base ionization when dissolved in water, yielding hydroxide and pyridinium ions:

The preceding ionization reactions suggest that water may function as both a base (as in its reaction with hydrogen fluoride) and an acid (as in its reaction with ammonia). Species capable of either donating or accepting protons are called amphiprotric, or more generally, amphoteric, a term that may be used for acids and bases per definitions other than the Brønsted-Lowry one. The equations below show the two possible acid-base reactions for two amphiprotic species, bicarbonate ion and water:

${\text{HCO}}_{3}{}^{-}\left(\text{aq}\right)+{\text{H}}_{2}\text{O}\left(\text{l}\right)\phantom{\rule{4em}{0ex}}{\text{CO}}_{3}{}^{2-}\left(\text{aq}\right)+{\text{H}}_{3}{\text{O}}^{+}\left(\text{aq}\right)$

${\text{HCO}}_{3}{}^{-}\left(\text{aq}\right)+{\text{H}}_{2}\text{O}\left(\text{l}\right)\phantom{\rule{4em}{0ex}}{\text{H}}_{2}{\text{CO}}_{3}\left(\text{aq}\right)+{\text{OH}}^{-}\left(\text{aq}\right)$

The first equation represents the reaction of bicarbonate as an acid with water as a base, whereas the second represents reaction of bicarbonate as a base with water as an acid. When bicarbonate is added to water, both these equilibria are established simultaneously and the composition of the resulting solution may be determined through appropriate equilibrium calculations, as described later in this chapter.

In the liquid state, molecules of an amphiprotic substance can react with one another as illustrated for water in the equations below:

The process in which like molecules react to yield ions is called autoionization. Liquid water undergoes autoionization to a very slight extent; at 25 °C, approximately two out of every billion water molecules are ionized. The extent of the water autoionization process is reflected in the value of its equilibrium constant, the ion-product constant for water, K_w:

${\text{H}}_{2}\text{O}\left(l\right)+{\text{H}}_{2}\text{O}\left(l\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+{\text{OH}}^{\text{−}}\left(aq\right)\phantom{\rule{5em}{0ex}}{K}_{\text{w}}=\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]\left[{\text{OH}}^{\text{−}}\right]$

The slight ionization of pure water is reflected in the small value of the equilibrium constant; at 25 °C, K_w has a value of 1.0 $×$ 10⁻¹⁴. The process is endothermic, and so the extent of ionization and the resulting concentrations of hydronium ion and hydroxide ion increase with temperature. For example, at 100 °C, the value for K_w is about 5.6 $×$ 10⁻¹³, roughly 50 times larger than the value at 25 °C.

Ion Concentrations in Pure Water What are the hydronium ion concentration and the hydroxide ion concentration in pure water at 25 °C?

Solution The autoionization of water yields the same number of hydronium and hydroxide ions. Therefore, in pure water, [H₃O⁺] = [OH⁻] = x. At 25 °C:

${K}_{\text{w}}=\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]\left[{\text{OH}}^{\text{−}}\right]=x=1.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-14}$

So:

$x=\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]=\left[{\text{OH}}^{\text{−}}\right]=\sqrt{1.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-14}}=1.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-7}\phantom{\rule{0.2em}{0ex}}M$

The hydronium ion concentration and the hydroxide ion concentration are the same, 1.0 $×$ 10⁻⁷M.

Check Your Learning The ion product of water at 80 °C is 2.4 $×$ 10⁻¹³. What are the concentrations of hydronium and hydroxide ions in pure water at 80 °C?

Answer:

[H₃O⁺] = [OH⁻] = 4.9 $×$ 10⁻⁷M

The Inverse Relation between [H₃O⁺] and [OH⁻] A solution of an acid in water has a hydronium ion concentration of 2.0 $×$ 10⁻⁶M. What is the concentration of hydroxide ion at 25 °C?

Solution Use the value of the ion-product constant for water at 25 °C

$2{\text{H}}_{2}\text{O}\left(l\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+{\text{OH}}^{\text{−}}\left(aq\right)\phantom{\rule{5em}{0ex}}{K}_{\text{w}}=\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]\left[{\text{OH}}^{\text{−}}\right]=1.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-14}$

to calculate the missing equilibrium concentration.

Rearrangement of the K_w expression shows that [OH⁻] is inversely proportional to [H₃O⁺]:

$\left[{\text{OH}}^{\text{−}}\right]=\phantom{\rule{0.2em}{0ex}}\frac{{K}_{\text{w}}}{\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]}\phantom{\rule{0.2em}{0ex}}=\phantom{\rule{0.2em}{0ex}}\frac{1.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-14}}{2.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-6}}\phantom{\rule{0.2em}{0ex}}=5.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-9}$

Compared with pure water, a solution of acid exhibits a higher concentration of hydronium ions (due to ionization of the acid) and a proportionally lower concentration of hydroxide ions. This may be explained via Le Châtelier’s principle as a left shift in the water autoionization equilibrium resulting from the stress of increased hydronium ion concentration.

Substituting the ion concentrations into the K_w expression confirms this calculation, resulting in the expected value:

${K}_{\text{w}}=\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]\left[{\text{OH}}^{\text{−}}\right]=\left(2.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-6}\right)\left(5.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-9}\right)=1.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}{10}^{-14}$

Check Your Learning What is the hydronium ion concentration in an aqueous solution with a hydroxide ion concentration of 0.001 M at 25 °C?

Answer:

[H₃O⁺] = 1 $×$ 10⁻¹¹M

Representing the Acid-Base Behavior of an Amphoteric Substance Write separate equations representing the reaction of ${\text{HSO}}_{3}{}^{\text{−}}$

(a) as an acid with OH⁻

(b) as a base with HI

Solution (a) ${\text{HSO}}_{3}{}^{\text{−}}\left(aq\right)+{\text{OH}}^{\text{−}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{SO}}_{3}{}^{\text{2−}}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)$

(b) ${\text{HSO}}_{3}{}^{\text{−}}\left(aq\right)+\text{HI}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{H}}_{2}{\text{SO}}_{3}\left(aq\right)+{\text{I}}^{\text{−}}\left(aq\right)$

Check Your Learning Write separate equations representing the reaction of ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}$

(a) as a base with HBr

(b) as an acid with OH⁻

Answer:

(a) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}\left(aq\right)+\text{HBr}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{PO}}_{4}\left(aq\right)+{\text{Br}}^{\text{−}}\left(aq\right);$ (b) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}\left(aq\right)+{\text{OH}}^{\text{−}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{HPO}}_{4}{}^{\text{2−}}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)$

Key Concepts and Summary

A compound that can donate a proton (a hydrogen ion) to another compound is called a Brønsted-Lowry acid. The compound that accepts the proton is called a Brønsted-Lowry base. The species remaining after a Brønsted-Lowry acid has lost a proton is the conjugate base of the acid. The species formed when a Brønsted-Lowry base gains a proton is the conjugate acid of the base. Thus, an acid-base reaction occurs when a proton is transferred from an acid to a base, with formation of the conjugate base of the reactant acid and formation of the conjugate acid of the reactant base. Amphiprotic species can act as both proton donors and proton acceptors. Water is the most important amphiprotic species. It can form both the hydronium ion, H₃O⁺, and the hydroxide ion, OH⁻ when it undergoes autoionization:

${\text{2H}}_{2}\text{O(}l\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{O}}^{+}\left(aq\right)+{\text{OH}}^{\text{−}}\left(aq\right)$

The ion product of water, K_w is the equilibrium constant for the autoionization reaction:

${K}_{\text{w}}=\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]\left[{\text{OH}}^{\text{−}}\right]=1.0\phantom{\rule{0.2em}{0ex}}×\phantom{\rule{0.2em}{0ex}}1{0}^{-14}\phantom{\rule{0.2em}{0ex}}\text{at}\phantom{\rule{0.2em}{0ex}}25\phantom{\rule{0.2em}{0ex}}\text{°C}$

Key Equations

K_w = [H₃O⁺][OH⁻] = 1.0 $×$ 10⁻¹⁴ (at 25 °C)

Chemistry End of Chapter Exercises

1. Write equations that show NH₃ as both a conjugate acid and a conjugate base.

One example for NH₃ as a conjugate acid: ${\text{NH}}_{2}{}^{\text{−}}+{\text{H}}^{\text{+}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{NH}}_{3};$ as a conjugate base: ${\text{NH}}_{4}{}^{\text{+}}\left(aq\right)+{\text{OH}}^{\text{−}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{NH}}_{3}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)$

2. Write equations that show ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}$ acting both as an acid and as a base.

3. Show by suitable net ionic equations that each of the following species can act as a Brønsted-Lowry acid:

(a) ${\text{H}}_{3}{\text{O}}^{\text{+}}$

(b) HCl

(c) NH₃

(d) CH₃CO₂H

(e) ${\text{NH}}_{4}{}^{\text{+}}$

(f) ${\text{HSO}}_{4}{}^{\text{−}}$

(a) ${\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}^{\text{+}}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right);$ (b) $\text{HCl}\left(\mathrm{aq}\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}^{\text{+}}\left(aq\right)+{\text{Cl}}^{\text{−}}\left(aq\right);$ (c) ${\text{NH}}_{3}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}^{\text{+}}\left(aq\right)+{\text{NH}}_{2}{}^{\text{−}}\left(aq\right);$ (d) ${\text{CH}}_{3}{\text{CO}}_{2}\text{H}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}^{\text{+}}\left(aq\right)+{\text{CH}}_{3}{\text{CO}}_{2}{}^{\text{−}}\left(aq\right);$ (e) ${\text{NH}}_{4}{}^{\text{+}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}^{\text{+}}\left(aq\right)+{\text{NH}}_{3}\left(aq\right);$ (f) ${\text{HSO}}_{4}{}^{\text{−}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}^{+}\left(aq\right)+{\text{SO}}_{4}{}^{\text{2−}}\left(aq\right)$

4. Show by suitable net ionic equations that each of the following species can act as a Brønsted-Lowry acid:

(a) HNO₃

(b) ${\text{PH}}_{4}{}^{\text{+}}$

(c) H₂S

(d) CH₃CH₂COOH

(e) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}$

(f) HS⁻

5. Show by suitable net ionic equations that each of the following species can act as a Brønsted-Lowry base:

(a) H₂O

(b) OH⁻

(c) NH₃

(d) CN⁻

(e) S²⁻

(f) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}$

(a) ${\text{H}}_{2}\text{O}\left(l\right)+{\text{H}}^{\text{+}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right);$ (b) ${\text{OH}}^{\text{−}}\left(aq\right)+{\text{H}}^{\text{+}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}_{2}\text{O}\left(l\right);$ (c) ${\text{NH}}_{3}\left(aq\right)+{\text{H}}^{\text{+}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{NH}}_{4}{}^{\text{+}}\left(aq\right);$ (d) ${\text{CN}}^{\text{−}}\left(aq\right)+{\text{H}}^{\text{+}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}\text{HCN}\left(aq\right);$ (e) ${\text{S}}^{2-}\left(aq\right)+{\text{H}}^{\text{+}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{HS}}^{\text{−}}\left(aq\right);$ (f) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}\left(aq\right)+{\text{H}}^{\text{+}}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{PO}}_{4}\left(aq\right)$

6. Show by suitable net ionic equations that each of the following species can act as a Brønsted-Lowry base:

(a) HS⁻

(b) ${\text{PO}}_{4}{}^{\text{3−}}$

(c) ${\text{NH}}_{2}{}^{\text{−}}$

(d) C₂H₅OH

(e) O²⁻

(f) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}$

7. What is the conjugate acid of each of the following? What is the conjugate base of each?

(a) OH⁻

(b) H₂O

(c) ${\text{HCO}}_{3}{}^{\text{−}}$

(d) NH₃

(e) ${\text{HSO}}_{4}{}^{\text{−}}$

(f) H₂O₂

(g) HS⁻

(h) ${\text{H}}_{5}{\text{N}}_{2}{}^{\text{+}}$

(a) H₂O, O²⁻; (b) H₃O⁺, OH⁻; (c) H₂CO₃, ${\text{CO}}_{3}{}^{\text{2−}};$ (d) ${\text{NH}}_{4}{}^{\text{+}},$ ${\text{NH}}_{2}{}^{\text{−}};$ (e) H₂SO₄, ${\text{SO}}_{4}{}^{\text{2−}};$ (f) ${\text{H}}_{3}{\text{O}}_{2}{}^{\text{+}},$ ${\text{HO}}_{2}{}^{\text{−}};$ (g) H₂S; S²⁻; (h) ${\text{H}}_{6}{\text{N}}_{2}{}^{2+},$ H₄N₂

8. What is the conjugate acid of each of the following? What is the conjugate base of each?

(a) H₂S

(b) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}$

(c) PH₃

(d) HS⁻

(e) ${\text{HSO}}_{3}{}^{\text{−}}$

(f) ${\text{H}}_{3}{\text{O}}_{2}{}^{\text{+}}$

(g) H₄N₂

(h) CH₃OH

9. Identify and label the Brønsted-Lowry acid, its conjugate base, the Brønsted-Lowry base, and its conjugate acid in each of the following equations:

(a) ${\text{HNO}}_{3}+{\text{H}}_{2}\text{O}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{O}}^{\text{+}}+{\text{NO}}_{3}{}^{\text{−}}$

(b) ${\text{CN}}^{\text{−}}+{\text{H}}_{2}\text{O}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}\text{HCN}+{\text{OH}}^{\text{−}}$

(c) ${\text{H}}_{2}{\text{SO}}_{4}+{\text{Cl}}^{\text{−}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}\text{HCl}+{\text{HSO}}_{4}{}^{\text{−}}$

(d) ${\text{HSO}}_{4}{}^{\text{−}}+{\text{OH}}^{\text{−}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{SO}}_{4}{}^{\text{2−}}+{\text{H}}_{2}\text{O}$

(e) ${\text{O}}^{2-}+{\text{H}}_{2}\text{O}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}2{\mathrm{OH}}^{\text{−}}$

(f) ${\left[\text{Cu}{\left({\text{H}}_{2}\text{O}\right)}_{3}\left(\text{OH}\right)\right]}^{\text{+}}+{\left[\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{6}\right]}^{3+}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\left[\text{Cu}{\left({\text{H}}_{2}\text{O}\right)}_{4}\right]}^{2+}+{\left[\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{5}\left(\text{OH}\right)\right]}^{2+}$

(g) ${\text{H}}_{2}\text{S}+{\text{NH}}_{2}{}^{\text{−}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{HS}}^{\text{−}}+{\text{NH}}_{3}$

10. The labels are Brønsted-Lowry acid = BA; its conjugate base = CB; Brønsted-Lowry base = BB; its conjugate acid = CA. (a) HNO₃(BA), H₂O(BB), H₃O⁺(CA), ${\text{NO}}_{3}{}^{\text{−}}\left(\text{CB}\right);$ (b) CN⁻(BB), H₂O(BA), HCN(CA), OH⁻(CB); (c) H₂SO₄(BA), Cl⁻(BB), HCl(CA), ${\text{HSO}}_{4}{}^{\text{−}}\left(\text{CB}\right);$ (d) ${\text{HSO}}_{4}{}^{\text{−}}\left(\text{BA}\right),$ OH⁻(BB), ${\text{SO}}_{4}{}^{\text{2−}}$ (CB), H₂O(CA); (e) O²⁻(BB), H₂O(BA) OH⁻(CB and CA); (f) [Cu(H₂O)₃(OH)]⁺(BB), [Al(H₂O)₆]³⁺(BA), [Cu(H₂O)₄]²⁺(CA), [Al(H₂O)₅(OH)]²⁺(CB); (g) H₂S(BA), ${\text{NH}}_{2}{}^{\text{−}}\left(\text{BB}\right),$ HS⁻(CB), NH₃(CA)

11. Identify and label the Brønsted-Lowry acid, its conjugate base, the Brønsted-Lowry base, and its conjugate acid in each of the following equations:

(a) ${\text{NO}}_{2}{}^{\text{−}}+{\text{H}}_{2}\text{O}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{HNO}}_{2}+{\text{OH}}^{\text{−}}$

(b) $\text{HBr}+{\text{H}}_{2}\text{O}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{O}}^{\text{+}}+{\text{Br}}^{\text{−}}$

(c) ${\text{HS}}^{\text{−}}+{\text{H}}_{2}\text{O}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}_{2}\text{S}+{\text{OH}}^{\text{−}}$

(d) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}+{\text{OH}}^{\text{−}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{HPO}}_{4}{}^{\text{2−}}+{\text{H}}_{2}\text{O}$

(e) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}+\text{HCl}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{PO}}_{4}+{\text{Cl}}^{\text{−}}$

(f) ${\left[\text{Fe}{\left({\text{H}}_{2}\text{O}\right)}_{5}\left(\text{OH}\right)\right]}^{2+}+{\left[\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{6}\right]}^{3+}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{[Fe}{\left({\text{H}}_{2}\text{O}\right)}_{6}\right]}^{3+}+{\left[\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{5}\left(\text{OH}\right)\right]}^{2+}$

(g) ${\text{CH}}_{3}\text{OH}+{\text{H}}^{\text{−}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{CH}}_{3}{\text{O}}^{\text{−}}+{\text{H}}_{2}$

12. What are amphiprotic species? Illustrate with suitable equations.

Amphiprotic species may either gain or lose a proton in a chemical reaction, thus acting as a base or an acid. An example is H₂O. As an acid: ${\text{H}}_{2}\text{O}\left(aq\right)+{\text{NH}}_{3}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{NH}}_{4}{}^{\text{+}}\left(aq\right)+{\text{OH}}^{\text{−}}\left(aq\right).$ As a base: ${\text{H}}_{2}\text{O}\left(aq\right)+\text{HCl}\left(aq\right)\phantom{\rule{0.2em}{0ex}}⇌\phantom{\rule{0.2em}{0ex}}{\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+{\text{Cl}}^{\text{−}}\left(aq\right)$

13. State which of the following species are amphiprotic and write chemical equations illustrating the amphiprotic character of these species:

(a) H₂O

(b) ${\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}$

(c) S²⁻

(d) ${\text{CO}}_{3}{}^{\text{2−}}$

(e) ${\text{HSO}}_{4}{}^{\text{−}}$

14. State which of the following species are amphiprotic and write chemical equations illustrating the amphiprotic character of these species.

(a) NH₃

(b) ${\text{HPO}}_{4}{}^{\text{−}}$

(c) Br⁻

(d) ${\text{NH}}_{4}{}^{\text{+}}$

(e) ${\text{ASO}}_{4}{}^{\text{3−}}$

amphiprotic: (a) ${\text{NH}}_{3}+{\text{H}}_{3}{\text{O}}^{\text{+}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{NH}}_{4}\text{OH}+{\text{H}}_{2}\text{O},$ ${\text{NH}}_{3}+{\text{OCH}}_{3}{}^{\text{−}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{NH}}_{2}{}^{\text{−}}+{\text{CH}}_{3}\text{OH};$ (b) ${\text{HPO}}_{4}{}^{\text{2−}}+{\text{OH}}^{\text{−}}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{PO}}_{4}{}^{\text{3−}}+{\text{H}}_{2}\text{O},$ ${\text{HPO}}_{4}{}^{\text{2−}}+{\text{HClO}}_{4}\phantom{\rule{0.2em}{0ex}}⟶\phantom{\rule{0.2em}{0ex}}{\text{H}}_{2}{\text{PO}}_{4}{}^{\text{−}}+{\text{ClO}}_{4}{}^{\text{−}};$ not amphiprotic: (c) Br⁻; (d) ${\text{NH}}_{4}{}^{\text{+}};$ (e) ${\text{AsO}}_{4}{}^{\text{3−}}$

15. Is the self-ionization of water endothermic or exothermic? The ionization constant for water (K_w) is 2.9 $×$ 10⁻¹⁴ at 40 °C and 9.3 $×$ 10⁻¹⁴ at 60 °C.

Glossary

acid ionization: reaction involving the transfer of a proton from an acid to water, yielding hydronium ions and the conjugate base of the acid

amphiprotic: species that may either donate or accept a proton in a Bronsted-Lowry acid-base reaction

amphoteric: species that can act as either an acid or a base

autoionization: reaction between identical species yielding ionic products; for water, this reaction involves transfer of protons to yield hydronium and hydroxide ions

base ionization: reaction involving the transfer of a proton from water to a base, yielding hydroxide ions and the conjugate acid of the base

Brønsted-Lowry acid: proton donor

Brønsted-Lowry base: proton acceptor

conjugate acid: substance formed when a base gains a proton

conjugate base: substance formed when an acid loses a proton

ion-product constant for water (K_w): equilibrium constant for the autoionization of water

License

Icon for the Creative Commons Attribution 4.0 International License

Learning Objectives

Key Concepts and Summary

Key Equations

Chemistry End of Chapter Exercises

Glossary

License

Share This Book