Hydrolysis of Salt Solutions

Learning Objectives

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

  • Predict whether a salt solution will be acidic, basic, or neutral
  • Calculate the concentrations of the various species in a salt solution
  • Describe the process that causes solutions of certain metal ions to be acidic


As we have seen in the section on chemical reactions, when an acid and base are mixed, they undergo a neutralization reaction. The word “neutralization” seems to imply that a stoichiometrically equivalent solution of an acid and a base would be neutral. This is sometimes true, but the salts that are formed in these reactions may have acidic or basic properties of their own, as we shall now see.

Acid-Base Neutralization

A solution is neutral when it contains equal concentrations of hydronium and hydroxide ions. When we mix solutions of an acid and a base, an acid-base neutralization reaction occurs. However, even if we mix stoichiometrically equivalent quantities, we may find that the resulting solution is not neutral. It could contain either an excess of hydronium ions or an excess of hydroxide ions because the nature of the salt formed determines whether the solution is acidic, neutral, or basic. The following four situations illustrate how solutions with various pH values can arise following a neutralization reaction using stoichiometrically equivalent quantities:

  1. A strong acid and a strong base, such as HCl(aq) and NaOH(aq) will react to form a neutral solution since the conjugate partners produced are of negligible strength:
    HCl(aq)+NaOH(aq)NaCl(aq)+H2O(l)\text{HCl}\left(aq\right)+\text{NaOH}\left(aq\right)\rightleftharpoons \text{NaCl}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)
  2. A strong acid and a weak base yield a weakly acidic solution, not because of the strong acid involved, but because of the conjugate acid of the weak base.
  3. A weak acid and a strong base yield a weakly basic solution. A solution of a weak acid reacts with a solution of a strong base to form the conjugate base of the weak acid and the conjugate acid of the strong base. The conjugate acid of the strong base is a weaker acid than water and has no effect on the acidity of the resulting solution. However, the conjugate base of the weak acid is a weak base and ionizes slightly in water. This increases the amount of hydroxide ion in the solution produced in the reaction and renders it slightly basic.
  4. A weak acid plus a weak base can yield either an acidic, basic, or neutral solution. This is the most complex of the four types of reactions. When the conjugate acid and the conjugate base are of unequal strengths, the solution can be either acidic or basic, depending on the relative strengths of the two conjugates. Occasionally the weak acid and the weak base will have the same strength, so their respective conjugate base and acid will have the same strength, and the solution will be neutral. To predict whether a particular combination will be acidic, basic or neutral, tabulated K values of the conjugates must be compared.


Stomach Antacids

Our stomachs contain a solution of roughly 0.03 M HCl, which helps us digest the food we eat. The burning sensation associated with heartburn is a result of the acid of the stomach leaking through the muscular valve at the top of the stomach into the lower reaches of the esophagus. The lining of the esophagus is not protected from the corrosive effects of stomach acid the way the lining of the stomach is, and the results can be very painful. When we have heartburn, it feels better if we reduce the excess acid in the esophagus by taking an antacid. As you may have guessed, antacids are bases. One of the most common antacids is calcium carbonate, CaCO3. The reaction,

CaCO3(s)+2HCl(aq)aCl2(aq)+H2O(l)+CO2(g){\text{CaCO}}_{3}\left(s\right)+2\text{HCl}\left(aq\right)\rightleftharpoons {\text{aCl}}_{2}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)+{\text{CO}}_{2}\left(g\right)

not only neutralizes stomach acid, it also produces CO2(g), which may result in a satisfying belch.

Milk of Magnesia is a suspension of the sparingly soluble base magnesium hydroxide, Mg(OH)2. It works according to the reaction:

Mg(OH)2(s)Mg2+(aq)+2OH-(aq)\text{Mg}{\left(\text{OH}\right)}_{2}\left(s\right)\rightleftharpoons {\text{Mg}}^{2+}\left(aq\right)+2{\text{OH}}^{\text{-}}\left(aq\right)

The hydroxide ions generated in this equilibrium then go on to react with the hydronium ions from the stomach acid, so that

H3O++OH-2H2O(l){\text{H}}_{3}{\text{O}}^{\text{+}}+{\text{OH}}^{\text{-}}\rightleftharpoons 2{\text{H}}_{2}\text{O}\left(l\right)

This reaction does not produce carbon dioxide, but magnesium-containing antacids can have a laxative effect.

Several antacids have aluminum hydroxide, Al(OH)3, as an active ingredient. The aluminum hydroxide tends to cause constipation, and some antacids use aluminum hydroxide in concert with magnesium hydroxide to balance the side effects of the two substances.

Culinary Aspects of Chemistry

Cooking is essentially synthetic chemistry that happens to be safe to eat. There are a number of examples of acid-base chemistry in the culinary world. One example is the use of baking soda, or sodium bicarbonate in baking. NaHCO3 is a base. When it reacts with an acid such as lemon juice, buttermilk, or sour cream in a batter, bubbles of carbon dioxide gas are formed from decomposition of the resulting carbonic acid, and the batter “rises.” Baking powder is a combination of sodium bicarbonate, and one or more acid salts that react when the two chemicals come in contact with water in the batter.

Many people like to put lemon juice or vinegar, both of which are acids, on cooked fish (Figure 1). It turns out that fish have volatile amines (bases) in their systems, which are neutralized by the acids to yield involatile ammonium salts. This reduces the odor of the fish, and also adds a “sour” taste that we seem to enjoy.

An image is shown of two fish with heads removed and skin on with lemon slices placed in the body cavity. Figure 1. A neutralization reaction takes place between citric acid in lemons or acetic acid in vinegar, and the bases in the flesh of fish.


Pickling is a method used to preserve vegetables using a naturally produced acidic environment. The vegetable, such as a cucumber, is placed in a sealed jar submerged in a brine solution. The brine solution favors the growth of beneficial bacteria and suppresses the growth of harmful bacteria. The beneficial bacteria feed on starches in the cucumber and produce lactic acid as a waste product in a process called fermentation. The lactic acid eventually increases the acidity of the brine to a level that kills any harmful bacteria, which require a basic environment. Without the harmful bacteria consuming the cucumbers they are able to last much longer than if they were unprotected. A byproduct of the pickling process changes the flavor of the vegetables with the acid making them taste sour.

Salts of Weak Bases and Strong Acids

When we neutralize a weak base with a strong acid, the product is a salt containing the conjugate acid of the weak base. This conjugate acid is a weak acid. For example, ammonium chloride, NH4Cl, is a salt formed by the reaction of the weak base ammonia with the strong acid HCl:

NH3(aq)+HCl(aq)NH4Cl(aq){\text{NH}}_{3}\left(aq\right)+\text{HCl}\left(aq\right)\longrightarrow {\text{NH}}_{4}\text{Cl}\left(aq\right)

A solution of this salt contains ammonium ions and chloride ions. The chloride ion has no effect on the acidity of the solution since HCl is a strong acid. Chloride is a very weak base and will not accept a proton to a measurable extent. However, the ammonium ion, the conjugate acid of ammonia, reacts with water and increases the hydronium ion concentration:

NH4+(aq)+H2O(l)H3O+(aq)+NH3(aq){\text{NH}}_{4}{}^{\text{+}}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+{\text{NH}}_{3}\left(aq\right)

The equilibrium equation for this reaction is simply the ionization constant. Ka, for the acid
NH4+:{\text{NH}}_{4}{}^{\text{+}}:


[H3O+][NH3][NH4+]=Ka\frac{\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]\left[{\text{NH}}_{3}\right]}{\left[{\text{NH}}_{4}{}^{\text{+}}\right]}={K}_{\text{a}}

We will not find a value of Ka for the ammonium ion in Ionization Constants of Weak Acids. However, it is not difficult to determine Ka for
NH4+{\text{NH}}_{4}{}^{\text{+}}
from the value of the ionization constant of water, Kw, and Kb, the ionization constant of its conjugate base, NH3, using the following relationship:

Kw=Ka×Kb{K}_{\text{w}}={K}_{\text{a}}\times {K}_{\text{b}}

This relation holds for any base and its conjugate acid or for any acid and its conjugate base.

Example 1: The pH of a Solution of a Salt of a Weak Base and a Strong Acid

Aniline is an amine that is used to manufacture dyes. It is isolated as aniline hydrochloride,
[C6H5NH3+]Cl\left[{\text{C}}_{6}{\text{H}}_{5}{\text{NH}}_{3}{}^{\text{+}}\right]\text{Cl}
, a salt prepared by the reaction of the weak base aniline and hydrochloric acid. What is the pH of a 0.233 M solution of aniline hydrochloride?

C6H5NH3+(aq)+H2O(l)H3O+(aq)+C6H5NH2(aq){\text{C}}_{6}{\text{H}}_{5}{\text{NH}}_{3}{}^{\text{+}}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+{\text{C}}_{6}{\text{H}}_{5}{\text{NH}}_{2}\left(aq\right)





Check Your Learning

  1. Do the calculations and show that the hydronium ion concentration for a 0.233-M solution of
    C6H5NH3+{\text{C}}_{6}{\text{H}}_{5}{\text{NH}}_{3}{}^{\text{+}}
    is 2.3
    ×\times
    10−3 and the pH is 2.64.
  2. What is the hydronium ion concentration in a 0.100-M solution of ammonium nitrate, NH4NO3, a salt composed of the ions
    NH4+{\text{NH}}_{4}{}^{\text{+}}
    and
    NO3-{\text{NO}}_{3}{}^{\text{-}}
    . Use the data in Table 2 on Relative Strengths of Acids and Bases to determine Kb for the ammonium ion. Which is the stronger acid
    C6H5NH3+{\text{C}}_{6}{\text{H}}_{5}{\text{NH}}_{3}{}^{\text{+}}
    or
    NH4+?{\text{NH}}_{4}{}^{\text{+}}?






Salts of Weak Acids and Strong Bases

When we neutralize a weak acid with a strong base, we get a salt that contains the conjugate base of the weak acid. This conjugate base is usually a weak base. For example, sodium acetate, NaCH3CO2, is a salt formed by the reaction of the weak acid acetic acid with the strong base sodium hydroxide:

CH3CO2H(aq)+NaOH(aq)NaCH3CO2(aq)+H2O(aq){\text{CH}}_{3}{\text{CO}}_{2}\text{H}\left(aq\right)+\text{NaOH}\left(aq\right)\longrightarrow {\text{NaCH}}_{3}{\text{CO}}_{2}\left(aq\right)+{\text{H}}_{2}\text{O}\left(aq\right)

A solution of this salt contains sodium ions and acetate ions. The sodium ion, as the conjugate acid of a strong base, has no effect on the acidity of the solution. However, the acetate ion, the conjugate base of acetic acid, reacts with water and increases the concentration of hydroxide ion:

CH3CO2-(aq)+H2O(l)CH3CO2H(aq)+OH-(aq){\text{CH}}_{3}{\text{CO}}_{2}{}^{\text{-}}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{CH}}_{3}{\text{CO}}_{2}\text{H}\left(aq\right)+{\text{OH}}^{\text{-}}\left(aq\right)

The equilibrium equation for this reaction is the ionization constant, Kb, for the base
CH3CO2-{\text{CH}}_{3}{\text{CO}}_{2}{}^{\text{-}}
. The value of Kb can be calculated from the value of the ionization constant of water, Kw, and Ka, the ionization constant of the conjugate acid of the anion using the equation:

Kw=Ka×Kb{K}_{\text{w}}={K}_{\text{a}}\times {K}_{\text{b}}

For the acetate ion and its conjugate acid we have:

Kb(forCH3CO2-)=KwKa(forCH3CO2H)=1.0×10141.8×105=5.6×1010{K}_{\text{b}}\left(\text{for}{\text{CH}}_{3}{\text{CO}}_{2}{}^{\text{-}}\right)=\frac{{K}_{\text{w}}}{{K}_{\text{a}}\left(\text{for}{\text{CH}}_{3}{\text{CO}}_{2}\text{H}\right)}=\frac{1.0\times {10}^{-14}}{1.8\times {10}^{-5}}=5.6\times {10}^{-10}

Some handbooks do not report values of Kb. They only report ionization constants for acids. If we want to determine a Kb value using one of these handbooks, we must look up the value of Ka for the conjugate acid and convert it to a Kb value.

Example 2: Equilibrium in a Solution of a Salt of a Weak Acid and a Strong Base

Determine the acetic acid concentration in a solution with
[CH3CO2-]=0.050M\left[{\text{CH}}_{3}{\text{CO}}_{2}{}^{\text{-}}\right]=0.050M
and [OH] = 2.5
×\times
10−6M at equilibrium. The reaction is:

CH3CO2-(aq)+H2O(l)CH3CO2H(aq)+OH-(aq){\text{CH}}_{3}{\text{CO}}_{2}{}^{\text{-}}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{CH}}_{3}{\text{CO}}_{2}\text{H}\left(aq\right)+{\text{OH}}^{\text{-}}\left(aq\right)





Check Your Learning

What is the pH of a 0.083-M solution of CN? Use 4.0
×\times
10−10 as Ka for HCN. Hint: We will probably need to convert pOH to pH or find
[H3O+]\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]
using [OH] in the final stages of this problem.





Equilibrium in a Solution of a Salt of a Weak Acid and a Weak Base

In a solution of a salt formed by the reaction of a weak acid and a weak base, to predict the pH, we must know both the Ka of the weak acid and the Kb of the weak base. If Ka > Kb, the solution is acidic, and if Kb > Ka, the solution is basic.

Example 3: Determining the Acidic or Basic Nature of Salts

Determine whether aqueous solutions of the following salts are acidic, basic, or neutral:

  1. KBr
  2. NaHCO3
  3. NH4Cl
  4. Na2HPO4
  5. NH4F






Check Your Learning

Determine whether aqueous solutions of the following salts are acidic, basic, or neutral:

  1. K2CO3
  2. CaCl2
  3. KH2PO4
  4. (NH4)2CO3
  5. AlBr3






The Ionization of Hydrated Metal Ions

If we measure the pH of the solutions of a variety of metal ions we will find that these ions act as weak acids when in solution. The aluminum ion is an example. When aluminum nitrate dissolves in water, the aluminum ion reacts with water to give a hydrated aluminum ion,
Al(H2O)63+\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{6}{}^{3+}
, dissolved in bulk water. What this means is that the aluminum ion has the strongest interactions with the six closest water molecules (the so-called first solvation shell), even though it does interact with the other water molecules surrounding this
Al(H2O)63+\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{6}{}^{3+}
cluster as well:

Al(NO3)3(s)+6H2O(l)Al(H2O)63+(aq)+3NO3-(aq)\text{Al}{\left({\text{NO}}_{3}\right)}_{3}\left(s\right)+6{\text{H}}_{2}\text{O}\left(l\right)\longrightarrow \text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{6}{}^{3+}\left(aq\right)+3{\text{NO}}_{3}{}^{\text{-}}\left(aq\right)

We frequently see the formula of this ion simply as “Al3+(aq)”, without explicitly noting the six water molecules that are the closest ones to the aluminum ion and just describing the ion as being solvated in water (hydrated). This is similar to the simplification of the formula of the hydronium ion,
H3O+{\text{H}}_{3}{\text{O}}^{\text{+}}
to H+. However, in this case, the hydrated aluminum ion is a weak acid (Figure 2) and donates a proton to a water molecule. Thus, the hydration becomes important and we may use formulas that show the extent of hydration:

Al(H2O)63+(aq)+H2O(l)H3O+(aq)+Al(H2O)5(OH)2+(aq)Ka=1.4×105\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{6}{}^{3+}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{5}{\left(\text{OH}\right)}^{2+}\left(aq\right){K}_{\text{a}}=1.4\times {10}^{-5}

As with other polyprotic acids, the hydrated aluminum ion ionizes in stages, as shown by:

Al(H2O)63+(aq)+H2O(l)H3O+(aq)+Al(H2O)5(OH)2+(aq)\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{6}{}^{3+}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{5}{\left(\text{OH}\right)}^{2+}\left(aq\right)


Al(H2O)5(OH)2+(aq)+H2O(l)H3O+(aq)+Al(H2O)4(OH)2+(aq)\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{5}{\left(\text{OH}\right)}^{2+}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{4}{\left(\text{OH}\right)}_{2}{}^{\text{+}}\left(aq\right)


Al(H2O)4(OH)2+(aq)+H2O(l)H3O+(aq)+Al(H2O)3(OH)3(aq)\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{4}{\left(\text{OH}\right)}_{2}{}^{\text{+}}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{3}{\left(\text{OH}\right)}_{3}\left(aq\right)

Note that some of these aluminum species are exhibiting amphiprotic behavior, since they are acting as acids when they appear on the right side of the equilibrium expressions and as bases when they appear on the left side.

A reaction is shown using ball and stick models. On the left, inside brackets with a superscript of 3 plus outside to the right is structure labeled “[ A l ( H subscript 2 O ) subscript 6 ] superscript 3 plus.” Inside the brackets is s central grey atom to which 6 red atoms are bonded in an arrangement that distributes them evenly about the central grey atom. Each red atom has two smaller white atoms attached in a forked or bent arrangement. Outside the brackets to the right is a space-filling model that includes a red central sphere with two smaller white spheres attached in a bent arrangement. Beneath this structure is the label “H subscript 2 O.” A double sided arrow follows. Another set of brackets follows to the right of the arrows which have a superscript of two plus outside to the right. The structure inside the brackets is similar to that on the left, except a white atom is removed from the structure. The label below is also changed to “[ A l ( H subscript 2 O ) subscript 5 O H ] superscript 2 plus.” To the right of this structure and outside the brackets is a space filling model with a central red sphere to which 3 smaller white spheres are attached. This structure is labeled “H subscript 3 O superscript plus.” Figure 3. When an aluminum ion reacts with water, the hydrated aluminum ion becomes a weak acid.
However, the ionization of a cation carrying more than one charge is usually not extensive beyond the first stage. Additional examples of the first stage in the ionization of hydrated metal ions are:

Fe(H2O)63+(aq)+H2O(l)H3O+(aq)+Fe(H2O)5(OH)2+(aq)Ka=2.74\text{Fe}{\left({\text{H}}_{2}\text{O}\right)}_{6}{}^{3+}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+\text{Fe}{\left({\text{H}}_{2}\text{O}\right)}_{5}{\left(\text{OH}\right)}^{2+}\left(aq\right){K}_{\text{a}}=2.74


Cu(H2O)62+(aq)+H2O(l)H3O+(aq)+Cu(H2O)5(OH)+(aq)Ka= 6.3\text{Cu}{\left({\text{H}}_{2}\text{O}\right)}_{6}{}^{2+}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+\text{Cu}{\left({\text{H}}_{2}\text{O}\right)}_{5}{\left(\text{OH}\right)}^{\text{+}}\left(aq\right){K}_{\text{a}}=~6.3


Zn(H2O)42+(aq)+H2O(l)H3O+(aq)+Zn(H2O)3(OH)+(aq)Ka=9.6\text{Zn}{\left({\text{H}}_{2}\text{O}\right)}_{4}{}^{2+}\left(aq\right)+{\text{H}}_{2}\text{O}\left(l\right)\rightleftharpoons {\text{H}}_{3}{\text{O}}^{\text{+}}\left(aq\right)+\text{Zn}{\left({\text{H}}_{2}\text{O}\right)}_{3}{\left(\text{OH}\right)}^{\text{+}}\left(aq\right){K}_{\text{a}}=9.6

Example 4: Hydrolysis of [Al(H2O)6]3+

Calculate the pH of a 0.10-M solution of aluminum chloride, which dissolves completely to give the hydrated aluminum ion
[Al(H2O)6]3+{\left[\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{6}\right]}^{3+}
in solution.





Check Your Learning

What is
[Al(H2O)5(OH)2+]\left[\text{Al}{\left({\text{H}}_{2}\text{O}\right)}_{5}{\left(\text{OH}\right)}^{2+}\right]
in a 0.15-M solution of Al(NO3)3 that contains enough of the strong acid HNO3 to bring
[H3O+]\left[{\text{H}}_{3}{\text{O}}^{\text{+}}\right]
to 0.10 M?





The constants for the different stages of ionization are not known for many metal ions, so we cannot calculate the extent of their ionization. However, practically all hydrated metal ions other than those of the alkali metals ionize to give acidic solutions. Ionization increases as the charge of the metal ion increases or as the size of the metal ion decreases.

Key Concepts and Summary

The characteristic properties of aqueous solutions of Brønsted-Lowry acids are due to the presence of hydronium ions; those of aqueous solutions of Brønsted-Lowry bases are due to the presence of hydroxide ions. The neutralization that occurs when aqueous solutions of acids and bases are combined results from the reaction of the hydronium and hydroxide ions to form water. Some salts formed in neutralization reactions may make the product solutions slightly acidic or slightly basic.

Solutions that contain salts or hydrated metal ions have a pH that is determined by the extent of the hydrolysis of the ions in the solution. The pH of the solutions may be calculated using familiar equilibrium techniques, or it may be qualitatively determined to be acidic, basic, or neutral depending on the relative Ka and Kb of the ions involved.

Exercises

  1. Determine whether aqueous solutions of the following salts are acidic, basic, or neutral:

    1. Al(NO3)3
    2. RbI
    3. KHCO2
    4. CH3NH3Br


  2. Determine whether aqueous solutions of the following salts are acidic, basic, or neutral:

    1. FeCl3
    2. K2CO3
    3. NH4Br
    4. KClO4


  3. Novocaine, C13H21O2N2Cl, is the salt of the base procaine and hydrochloric acid. The ionization constant for procaine is 7
    ×\times
    10−6. Is a solution of novocaine acidic or basic? What are [H3O+], [OH], and pH of a 2.0% solution by mass of novocaine, assuming that the density of the solution is 1.0 g/mL.






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