Chemical Foundations of Biological Systems

MCAT-3200184 book November 13, 2015 15:28 MHID: 1-25-958837-8 ISBN: 1-25-958837-2
UNIT II
Chemical Foundations
of Biological Systems
Foundational Concept: The principles that govern chemical interactions and

reactions form the basis for a broader understanding of the molecular dynamics
of living systems.
CHAPTER 6 The Unique Nature of Water and Its Solutions

CHAPTER 7 The Nature of Molecules and Intermolecular Interactions
CHAPTER 8 Separation and Purification Methods
CHAPTER 9 Structure, Function, and Reactivity of Biologically
Relevant Molecules
CHAPTER 10 Principles of Chemical Thermodynamics and Kinetics
Unit II MINITEST
CHAPTER 6
The Unique Nature

of Water and
Its Solutions
Read This Chapter to Learn About

➤ Acid–Base Reactions
➤ Ions in Solutions
➤ Solubility
➤ Acid–Base Titrations
ACID–BASE REACTIONS
An acid reacts with a base to form an ionic compound, often called a salt, plus water.
Brønsted–Lowry Definition of Acids and Bases

ACIDS
An acid is a compound that produces H+ (hydronium ion) in water solution. There are
strong acids and weak acids. A strong acid is defined as an acid that dissociates fully
into two ions in water solution.
The six strong acids are HCl, HBr, HI, HNO3 , H2 SO4 , and HClO4 .
All other acids are weak acids, defined as an acid that dissociates only to a very
small extent in water solution. Some examples are HF, HCN, H2 CO3 , H3 PO4 , acetic
acid, and oxalic acid.
175
176
UNIT II: BASES
Chemical
Foundations of A base is a compound that produces OH− (hydroxide ion) in water solution. There are
Biological Systems strong bases and weak bases. A strong base fully dissociates into its ions in water solu-
tion. Among the strong bases are hydroxides of groups IA and IIA that are fully soluble
in water. They are LiOH, NaOH, KOH, and Ba(OH)2 .
There are many weak bases, but most of them are organic analogs of ammonia,
NH3 . Ammonia dissolves in water, but only a very small percentage of NH3 molecules
produce NH4 OH, which then dissociates into NH+ 4 and OH .
−
TYPES OF ACID–BASE REACTIONS

When a strong acid reacts with a strong base, the ionic compound that forms is neutral
in water solution. The ionic compound is formed by taking the cation from the base
and the anion from the acid.
HCl + KOH → KCl + H2 O KCl is neutral.

H2 SO4 + NaOH → NaHSO4 + H2 O NaHSO4 is neutral.
When a strong acid reacts with a weak base, the ionic compound that forms is
acidic in water solution.
HCl + NH4 OH → NH4 Cl + H2 O NH4 Cl is acidic.

HClO4 + NH4 OH → NH4 ClO4 + H2 O NH4 ClO4 is acidic.
When a weak acid reacts with a strong base, the ionic compound that forms is basic
in water solution.
HF + NaOH → NaF + H2 O NaF is basic.
HCN + KOH → KCN + H2 O KCN is basic.
Compounds, such as water, that can serve as an acid (donates a proton) or base
(accepts a proton) are referred to as amphiprotic compounds.
Ionization of Water
Acidity is a measure of the concentration of H+ in a dilute water solution. It is mea-
sured using the pH scale, which is based on a process that water undergoes called
autoionization:
H2 O (l) H+ (aq) + OH− (aq) K w = 1 × 10−14
This is an equilibrium process that lies very far to the left. The K for this, in other
words, is very small. It is called K w (for water) and K w = 1 × 10−14 at 25 ◦ C. This means
that approximately 1 out of every 1014 molecules dissociates into ions in this manner.
An acid produces H+ in water solution. A base produces OH− (hydroxide) in water
solution. When an acid reacts with a base, a salt is formed. This chapter discusses these
compounds and their interactions.
177
The pH Scale CHAPTER 6:

The Unique Nature
The pH scale is from 0 to 14. It is a logarithmic scale (powers of 10). Each pH is 10-fold of Water and
Its Solutions
less acidic than the next lower pH value.
At pH 7, a solution is neutral.
[H+ ] = [OH− ]
Writing the K expression,
K w = [H+ ] [OH− ] = 1 × 10−14
At pH 7,
[H+ ] = [OH− ] = 1 × 10−7 M
From this, you can see that the pH = − log [H+ ] and that pOH = − log [OH− ].
When the pH is 7, the pOH is 7 as well.
pH + pOH = 14
When [H+ ] = 1 × 10−3 M, the pH = 3; and when [OH− ] = 1 × 10−11 M, the

pOH = 11.
EXAMPLE: Calculate the pH if [H+ ] is 3.5 × 10−5 M.
SOLUTION:
➤ Because the exponent is −5, the pH is near 5.

➤ pH = − log (3.5 × 10−5 ) = 4.5
EXAMPLE: Calculate [H+ ] when pH = 8.4.
SOLUTION:
➤ 8.4 = − log [H+ ]
➤ [H+ ] = 10−8.4 = 4 × 10−9 M
EXAMPLE: Calculate [OH− ] when pH = 10.6.
SOLUTION:
➤ pOH = 14 – 10.6 = 3.4
➤ [OH− ] = 10−3.4 = 4 × 10−4 M
Conjugate Acids and Bases

A Brønsted–Lowry acid, which is a proton donor, can be represented in general as HX
and a Brønsted–Lowry base, which is a proton acceptor, can be represented as X− . The
general reaction of an acid placed in water would be described in the following form:
HX + H2 O → X− + H3 O+
acid + base → base + acid
178
UNIT II: where the acid (HX) donates a proton to water (which acts as a base) to yield H3 O+ ,
Chemical which is a hydronium ion (a water molecule that has accepted a donated proton). HX
Foundations of
and X− are often referred to as a conjugate acid–base pair defined as a pair of com-
Biological Systems
pounds that differ in structure by one proton. HX is a conjugate acid while X− is the
conjugate base. The acid, which has the proton to donate, is the conjugate acid, while
the base, which is ready to accept the proton, is the conjugate base.
An example of a reaction involving an acid is:
HCl + H2 O → Cl− + H3 O+
(hydrochloric acid) + (water) → (chloride ion) + (hydronium ion)
acid + base → base + acid
The same process applies when a base is placed in water, which yields the general
reaction:
X− + H2 O → HX + OH−
base + acid → acid + base
where the base (X− ) accepts a proton from water (which acts as an acid) to yield the
conjugate acid of the base and OH− (hydroxide ion). An example of a reaction involving
a base is:
NH3 + H2 O → NH+
4 + OH
−
(ammonia) + (water) → (ammonium ion) + (hydroxide ion)

base + acid → acid + base
Strong Acids and Bases

STRONG ACIDS
A strong acid is an acid where every molecule dissociates into H+ and the counter
ion (the conjugate base). There are six strong acids–-HCl, HBr, HI, HNO3 , H2 SO4 , and
HClO4 .
The equation for the dissociation of HCl is written:
HCl (aq) → H+ (aq) + Cl− (aq)
Because there is no reverse reaction taking place, strong acids do not involve any
equilibrium process. Simple stoichiometry suffices. The concentration of the proton
and the concentration of the conjugate base Cl− are equal to the initial concentration
of the acid.
If 1,000 HCl molecules are dissolved in water, they dissociate into 1,000 H+ and
1,000 Cl− ions.
179
STRONG BASES CHAPTER 6:
The Unique Nature
If the base is a strong base, every molecule dissociates into ions in water solution. The of Water and
most common strong bases are LiOH, NaOH, KOH, and Ba(OH)2 . Its Solutions
KOH (aq) → K+ (aq) + OH− (aq)
Ba(OH)2 (aq) → Ba2+ (aq) + 2 OH− (aq)
There is no equilibrium here; stoichiometry suffices to determine [OH− ] and, thus,

pH. For LiOH, KOH, and NaOH, the base concentration equals the hydroxide
concentration.
[KOH] = [OH− ]
For Ba(OH)2 , the base concentration is half of the hydroxide concentration.

1
[Ba(OH)2 ] = [OH− ]
2
EXAMPLE: Calculate the pH of 0.065 M KOH. This is a strong base with 1 : 1
stoichiometry.
SOLUTION:
➤ [KOH] = [OH− ] = 0.065 M.

➤ pOH = − log 0.065 = 1.2
➤ pH = 14 − 1.2 = 12.8
EXAMPLE: Calculate the pH of 0.065 M Ba(OH)2 . This is a strong base with 1 : 2

stoichiometry.
SOLUTION:
1
➤ [Ba(OH)2 ] = [OH− ] = 0.065
2
➤ [OH− ] = 0.13 M
➤ pOH = − log 0.13 = 0.9
➤ pH = 14 − 0.9 = 13.1
Weak Acids and Bases

WEAK ACIDS
Weak acids have the word acid as part of their name, and they are not one of the six
strong acids.
For weak acids, only 1 out of every 10,000–100,000 molecules undergoes dissocia-
tion to proton and conjugate base or
HA (aq) H+ (aq) + A− (aq)

180
UNIT II: Most of the molecules are still in the HA form. This is an equilibrium process, with
Chemical a very small K a (for acid). The K a values are typically in the range of 10−4 to 10−6 . The
Foundations of K a expression is written as:
Biological Systems
[H+ ] [A− ]
Ka =
[HA]
EXAMPLE: Calculate the pH of 0.15 M HNO3 .
SOLUTION:
➤ This is a strong acid, so the proton concentration is equal to the acid
concentration: [H+ ] = [HNO3 ] = 0 .15 M.
➤ pH = − log 0.15 = 0.8
EXAMPLE: Calculate the pH of 0.15 M HF. For this problem, K a = 6.7 × 10−4 .
SOLUTION: This is a weak acid. The steps for solving this problem are:
➤ Write the equation.

HF (aq) H+ (aq) + F− (aq)
➤ Fill in the table.

HF H+ + F−
At equilibrium 0.15 M x x
(Small K so the initial HF concentration equals the HF concentration at
equilibrium.)
➤ Write the K expression.
[H+ ] [F− ]
Ka =
[HF]
➤ Fill in the equilibrium values.
x2
6.7 × 10−4 =
0.15
➤ Solve the [H+ ] for x.
x = [H+ ] = 1 × 10−2 M
➤ Calculate the pH.
pH = − log (1 × 10−2 ) = 2
WEAK BASES
We use ammonia for the weak base problems because almost all weak bases are organic
derivatives of ammonia. When ammonia is dissolved in water, approximately 1 out of
every 100,000 molecules produces an OH− (hydroxide ion).
The equation is:
NH3 (aq) + H2 O (aq) NH+ −
4 (aq) + OH (aq)
181
This is an equilibrium process and the K b (for base) is 1.8 × 10−5 . The K b expression CHAPTER 6:
is written: The Unique Nature
of Water and
[NH4 + ] [OH− ] Its Solutions
Kb =
[NH3 ]
EXAMPLE: Calculate the pH of 0.065 M NH3 . In this example, K b = 1.8 × 10−5 .
SOLUTION: This is a weak base; there are certain steps to follow.

NH3 (aq) + H2 O (l) NH+ −
4 (aq) + OH (aq)

NH3 NH+
4 + OH−
[NH+ −
4 ] [OH ]
Kb =
[NH3 ]
➤ Fill in the equilibrium values.
➤ Solve for x, i.e., [OH− ].
x2
1.8 × 10−5 =
0.065
x = [OH− ] = 1.1 × 10−3 M
➤ Calculate the pOH.

pOH = 3

pH = 11
POLYPROTIC ACIDS
Polyprotic acids are acids that have more than one proton; therefore, they have more
than one K a . There is just one K a per proton removed. In the following equations, all
substances are in aqueous solution.
➤ Carbonic acid has 2 protons (both weak):

H2 CO3
➤ For the removal of the first proton,
H2 CO3 H+ + HCO3 −1
➤ For the removal of the second proton,

HCO3 −1 H+ + CO3 −2
182
UNIT II: ➤ K a1 for the first proton = 4.3 × 10−7 Weak acid
Chemical
➤ K a2 for the second proton = 4.8 × 10−11 Weaker acid
Foundations of
Biological Systems ➤ Phosphoric acid has 3 protons (all weak):
H3 PO4
➤ Removal of first proton,
H3 PO4 H+ + H2 PO4 −1 K a1 = 6.9 ×10−3

3H → 2H
➤ Removal of second proton,
H2 PO4 −1 H+ + HPO4 −2 K a2 = 6.2 × 10−8

2H → 1H
➤ Removal of third proton,
HPO4 −2 H+ + PO4 −3 K a3 = 4.8 × 10−13
1H → 0H
pH OF A POLYPROTIC ACID SOLUTION

If you are calculating the pH of a solution of carbonic acid or phosphoric acid, only
the first (and largest) K a1 is used. The amount of proton produced by the subsequent
K a values is negligible compared to the first. In all of the equations that follow, every
substance is in aqueous solution except the water, which is liquid.
SALTS OF POLYPROTIC ACIDS

NaHCO3 is the salt of NaOH and H2 CO3 . It is a basic salt (K b ); thus, it produces OH−
and a conjugate acid:
HCO3 −1 + H2 O OH− + H2 CO3 K b1 = 2.3 × 10−8
Na2 CO3 is also a salt of NaOH and H2 CO3 . It is a basic salt (K b ); thus, it produces
OH− and a conjugate acid:
CO3 −2 + H2 O OH− + HCO3 −1 K b2 = 2.1 × 10−4
There are three salts of phosphoric acid:
NaH2 PO4
Na2 HPO4
Na3 PO4
All of these are basic salts; they produce OH− and a conjugate acid
H2 PO4 −1 + H2 O OH− + H3 PO4 K b1 = 1.4 × 10−12

HPO4 −2 + H2 O OH− + H2 PO4 −1 K b2 = 1.6 × 10−7
PO4 −3 + H2 O OH− + HPO4 −2 K b3 = 2.1 × 10−2
183
EXAMPLE: Calculate the pH of 0.1185 M phosphoric acid solution. CHAPTER 6:
The Unique Nature
SOLUTION:
of Water and
➤ For the pH of a polyprotic acid, we use only the K a1 . Its Solutions
K a1 = 6.9 × 10−3
H3 PO4 H+ + H2 PO4 −1
−1
H3 PO4 H+ + H2 PO4
0.1185 M x x
➤ Write K a expression.
[H+ ] [H2 PO4 −1 ]
Ka =
[H3 PO4 ]
➤ Fill in values and solve for x.
x2
6.9 × 10−3 =
0.1185 M

x = [H+ ] = 8.2 × 10−4 = 2.9 × 10−2 M

pH = − log[H+ ] = 1.5
EXAMPLE: Calculate the pH of 0.0165 M sodium hydrogen phosphate.
SOLUTION:
➤ Write the formula.
Na2 HPO4
➤ Recognize that this is a basic salt, so it is a base. So you need a K b .
HPO4 −2 + H2 O OH− + H2 PO4 −1
−2 −1
HPO4 OH− + H2 PO4
0.0165 M x x
➤ Determine which K b is needed.
K b1 involves 2H → 3H
➤ Because our salt has 1H and is going to the conjugate acid with 2H, we
need K b2 .
K b2 = 1.6 × 10−7
184
UNIT II: ➤ Write the K b expression.
Chemical
[OH− ] [H2 PO4 − ]
Foundations of K b2 =
Biological Systems [HPO4 −2 ]
➤ Fill in the values and solve for x.
x2
1.6 × 10−7 =
0.0165 M
x = [OH− ] = 5.1 × 10−5 M
➤ Calculate pOH and pH.
pOH = 4.3
pH = 9.7
SOLUTIONS OF SALTS
When an acid reacts with a base, in stoichiometric quantities, an ionic compound
(a salt) is formed, along with water:
acid + base → salt + H2 O
The ionic compound is neutral, acidic, or basic (when dissolved in water), depend-
ing on which acid and base were used to make it.
CASE 1:
Strong acid + Strong base −→ Neutral salt pH = 7
CASE 2:
Strong acid + Weak base −−→ Acidic salt pH < 7
CASE 3:
Weak acid + Strong base −→ Basic salt pH > 7
We look next at salts from cases 2 and 3 only. In the following equations, all sub-
stances are in aqueous solution except water, which is liquid.
CASE 2 EXAMPLES:
HCl + NH4 OH −→ NH4 Cl + H2 O
HNO3 + NH4 OH −→ NH4 NO3 + H2 O
CASE 3 EXAMPLES:
HF + LiOH −→ LiF + H2 O
HCN + KOH −→ KCN + H2 O

CH3 COOH + KOH− −→ CH3 COO− K+ + H2 O
185
ACIDIC SALTS CHAPTER 6:
The Unique Nature
Acidic salts are formed when a strong acid reacts with a weak base, as in case 2. of Water and
Its Solutions
EXAMPLE: Calculate the pH of 0.078 M ammonium nitrate. For this problem,
K a = 5.6 × 10−10 .
SOLUTION:
➤ Recognize that NH4 NO3 is an acidic salt.

➤ Therefore, it is an acid (produces H+ ).
NH+ +
4 (aq) NH3 (aq) + H (aq)

NH+
4 NH3 + H+
[NH3 ] [H+ ]
Ka =
[NH+
4]
➤ Fill in the values and solve for x, the [H+ ].

x2
5.6 × 10−10 =
0.078 M
x = [H ] = 6.6 × 10−6 M
+
➤ Calculate pH.
pH = 5.2
BASIC SALTS
Basic salts are formed when a strong base reacts with a weak acid, as in case 3.
EXAMPLE: Calculate the pH of 0.035 M KCN. For this problem, K b = 1.6 × 10−5 .
SOLUTION:
➤ Recognize that KCN is a basic salt.

➤ Therefore, it is a base (produces OH− ).
➤ Write the equation. The only ion here that can produce OH− from water is
the cyanide. You must have a negative ion to remove the H+ from H2 O,
leaving OH− .
CN− (aq) + H2 O (l) HCN (aq) + OH− (aq)

CN− HCN + OH−
186
UNIT II: ➤ Write the K expression.
Chemical [HCN] [OH− ]
Foundations of Kb =
[CN− ]
Biological Systems
➤ Fill in the values and solve for x, the [OH− ].
x2
1.6 × 10−5 =
0.035 M
x = [OH− ] = 7.5 × 10−4 M
➤ Calculate pOH.
pOH = 3.1
➤ Calculate pH.
pH = 10.9
Equilibrium Constants
You have just examined the equilibrium constants K a and K b for various acids and
bases. Now see how they work together to produce the ionization constant for water,
K w . First consider the K a expression for an acid and the K b expression for a base:
[H3 O+ ][A− ] [HA][OH− ]
Ka = and Kb =
HA [A− ]
When you multiply K a by K b, you get K a × K b = [H3 O+ ][OH− ] = K w = 1 × 10−14 .
Prove it to yourself by multiplying the K a value of HF (7.2 × 10−4 ) by the K b value of
F− (1.4 × 10−11 ).
One other equilibrium constant to be examined in this chapter is the solubility
product constant of a slightly soluble salt, K sp . Keep in mind that this is an equilib-
rium constant between the ionic compound and a saturated solution of the ions that it
forms. Consider the slight ability of AgCl (s) to dissolve in water. The equation for this is
AgCl (s) → Ag+ (aq) + Cl− (aq). When you write the equilibrium constant expressions
for a reaction, solids, liquids, and solvents are not included. This expression is written
as K sp = [Ag+ ][Cl− ] and has a value of 1.8 × 10−10 . When comparing this to the K sp
for CaSO4 (2.4 × 10−5 ), you see that the calcium sulfate is more soluble than the silver
chloride.
Buffers
DEFINITION OF COMMON BUFFER SYSTEMS
A buffer is a solution that resists change in pH when small amounts of acid or base are
added. It is usually a solution that is made of approximately equal concentrations of
an acid and its conjugate base. The calculation of the pH of a buffer uses exactly the
same method as for a common ion.
187
EXAMPLE: Calculate the pH of a buffer made by mixing 60.0 milliliters (mL) of CHAPTER 6:
0.100 M NH3 with 40.0 mL of 0.100 M NH4 Cl. The equilibrium constant, K a , is The Unique Nature
of Water and
K a = 5.6 × 10−10 Its Solutions
SOLUTION:
➤ Calculate the molarity of each component in the mixture.
(0.0600 L) (0.100 M) = 0.006 mole/0.100 L = 0.060 M NH3
(0.0400 L) (0.100 M) = 0.004 mole/0.100 L = 0.040 M NH4 Cl
➤ Write the equation and fill in the values.

NH4 H+ + NH3
Initial 0.040 M 0 0.060 M
−x +x +x
At equilibrium 0.040 M − x x 0.060 M + x

➤ Assume the change is negligible.
➤ Write the K a expression.
[H+ ] [NH3 ]
Ka =
[NH4 + ]
➤ Plug in the values and solve for x.
x (0.060)
5.6 × 10−10 =
0.040
x = [H ] = 3.7 × 10−10 M
+
pH = 9.4
INFLUENCE OF BUFFERS ON A TITRATION CURVE

While titration curves will be covered in more detail later in this chapter, you can use a
titration curve to show the impact of a buffer on a solution and how it resists changes
in pH. Buffers resist change in pH because they contain an acidic component to neu-
tralize OH− ions and a basic component to neutralize H+ ions. Consider the following
situation where a different number of moles of HCl in 1 liter of solution produce var-
ious pH values (see Figure 6-1). If a buffer is made from 0.2 M acetic acid and 0.2 M
sodium acetate, you can see that adding a small amount of the acid has little effect on
the pH, causing the line to remain more horizontal. In order for the line to remain hor-
izontal, the buffer concentration must be sufficiently larger than the amount of acid
being added.
Even if the buffer were made with half the concentration of acetic acid and sodium
acetate, 0.1 M each, the 0.1 M HCl solution would have a pH of 2.72—still shy of the pH
of 1 if there was no buffer present at all.
188
UNIT II:
7
Chemical
Foundations of
6
Biological Systems
5 Buffer 1 HCI
pH
4
3
Purewater
Pure water11HCI
HCI
2
1
1027 1026 1025 1024 1023 1022 1021 100
Moles of HCI added
per liter (CHCI )
FIGURE 6-1 Influence of buffers on a titration curve.
IONS IN SOLUTIONS
Anions and Cations
When an ionic compound is dissolved in a solution, there is a formation of both nega-
tive and positive ions. The negative ions are called anions, while the positive ions are
called cations. For example, when a salt such as sodium chloride is added to water, you
get Na+ and Cl− as the cation and anion, respectively.
NOMENCLATURE OF IONIC COMPOUNDS

Ionic compounds consist of cations and anions. The name of the cation comes first,
and it is named as the element. There are a few complex cations, but the most impor-
tant one is ammonium ion, which has the formula NH4 +1 .
The main group elements form cations in a systematic manner. Elements from
group I always form +1 cations. Elements from group II always form +2 cations. The
metals Al and Ga from group III always form +3 cations. In general, the metals always
form cations.
Anions are generally formed from nonmetals, or groups of nonmetals that are
covalently bonded. The simple cations and anions and many of the complex anions
are listed in the following table.
To name a compound such as Na3 N, the cation Na+1 is called sodium and the
anion N−3 is called nitride. Therefore, the compound is sodium nitride. AlN is alu-
minum nitride; Mg3 N2 is magnesium nitride; and MgO is magnesium oxide.
To write the formula of calcium hydride, the calcium cation is Ca+2 and the anion
hydride is H−1 . Two hydrides are required to balance the +2 charge on the calcium ion,
in order to net out to zero overall. So the formula is CaH2 .
189
TABLE 6-1 Simple and Complex Anions and Cations CHAPTER 6:
The Unique Nature
Main Group Cations and Simple Anions
of Water and
Group IA IIA IIIA IVA VA VIA VIIA Its Solutions
H+ H−
Hydrogen Hydride
Li+ Be2+ Al3+ N3− O2− F−
Lithium Beryllium Aluminum Nitride Oxide Fluoride
Na+ Mg2+ Ga3+ S2− Cl−
Sodium Magnesium Gallium Sulfide Chloride
K+ Ca2+ In3+ Se2− Br−
Potassium Calcium Indium Selenide Bromide
Rb+ Sr2+ Te2− I−
Rubidium Strontium Telluride Iodide
Cs+ Ba2+
Cesium Barium
Complex Anions
Cyanide CN−
Hydroxide OH−
Peroxide O2 −2
Permanganate MnO4 −
Chromate CrO4 −2
Dichromate Cr2 O7 −2
Carbonate CO3 −2 Hydrogen carbonate HCO3 −
Phosphate PO4 −3 Hydrogen phosphate HPO4 −2 Dihydrogen phosphate H2 PO4 −
Phosphite PO3 −3 Hydrogen phosphite HPO3 −2 Dihydrogen phosphite H2 PO3 −
Sulfate SO4 −2 Hydrogen sulfate HSO4 −
Sulfite SO3 −2 Hydrogen sulfite HSO3 −
Nitrate NO3 −
Nitrite NO2 −
Perchlorate ClO4 − Perbromate BrO4 − Periodate IO4 −
Chlorate ClO3 − Bromate BrO3 − Iodate IO3 −
Chlorite ClO2 − Bromite BrO2 − Iodite IO2 −
Hypochlorite ClO− Hypobromite BrO− Hypoiodite IO−
Complex Cation
Ammonium NH4 +
A good method to determine how many cations and how many anions are in a for-
mula is the lowest common denominator method. The lowest common denominator
of the charges is determined (ignoring the signs). This gives the total + charges and the
total − charges necessary.
EXAMPLE: Determine the formula of sodium oxide.
SOLUTION: Sodium is Na+1 and oxide is O−2 . The lowest common denominator
of 1 and 2 (the charges) is 2. Thus, the positive charges must total +2 and the
negative charges must total −2. So there must be 2 sodium cations and 1 oxide
anion, and the formula is Na2 O.
190
UNIT II: Transition metal cations vary in their possible charges; the charge of the metal
Chemical must be written in the name as a roman numeral. Thus, copper (II) oxide means
Foundations of that the copper cation is Cu+2 . Because oxide is always O−2 , the charges balance,
Biological Systems
and the formula is CuO.
Copper (I) oxide means that the copper cation is Cu+1 . Oxide is O−2 . The lowest
common denominator is 2; thus, there must be two Cu+1 cations for every oxide
anion. The formula is Cu2 O.
The complex anions must be memorized. Their names, formulas, and net
charge are given in the previous table.
EXAMPLE: Write the formula of sodium phosphate.
SOLUTION: The sodium cation is Na+1 and the phosphate anion is PO4 −3 . The
lowest common denominator of the charges is 3. Thus, there must be 3 sodium
cations and 1 phosphate anion to result in a net zero charge for the molecule. So
the formula is Na3 PO4 .
HYDRATION AND THE HYDRONIUM ION

When a water solution contains cations and anions, the water molecules will orient
themselves depending on whether an anion or cation is nearby. Because water is a
polar molecule where oxygen is the negative end, the oxygen of a water molecule will be
oppositely attracted to a cation. When a water molecule is oriented toward an
anion, the hydrogen atoms of the water molecule will be attracted to the anion. This is
because the hydrogen atoms of the water molecule are the positive ends of the molecule
and will be attracted to the negative anions. When the ions are surrounded or solvated
by water molecules, they are called hydrated ions.
Hydrogen ions can also interact with a water molecule. This is found in acid–base
chemistry when a proton is in solution. When in solution, the hydrogen ions (protons)
will form a coordinate covalent bond to a free pair of electrons on the oxygen atom
of a water molecule. This forms the hydronium ion as shown in the reaction
H+ + H2 O → H3 O+ .
SOLUBILITY
Concentration Units
There are various concentration units that can be used to describe how much solute
is dissolved in a certain amount of solution. This section deals with reactions that take
place in solution. The concentration unit that is used to make solutions for reaction is
molarity, which has the symbol M, and is defined as:
M = mole solute/liter (L) solution

191
This definition is also a working equation. There are three variables; if two are known, CHAPTER 6:
the third can be calculated. The Unique Nature
of Water and
EXAMPLE: Calculate the molarity of a solution that is prepared by dissolving 1.192 Its Solutions
grams (g) of oxalic acid (C2 H2 O4 ) in water to a total of 100.0 milliliters (mL) of
solution.
SOLUTION:
1. Convert the mass of oxalic acid to moles.
(1.192 g) (1 mole/90.04 g) = 0.01324 mole oxalic acid
2. Convert the milliliters to liters.

(100.0 mL) (1 L/1000 mL) = 0.1000 L
3. Calculate the molarity.

M = 0.01324 mole/0.1000 L = 0.1324 M
Solubility Product Constant

Insoluble ionic compounds are actually soluble to a very small extent. These solubili-
ties are equilibrium-based processes, with a very small equilibrium constant K .
The solubility equation is written with the solid on the left and the ions in solution
on the right, as shown in the following examples:
CaC2 O4 (s) Ca+2 (aq) + C2 O4 −2 (aq)

PbI2 (s) Pb+2 (aq) + 2I− (aq)
Ca3 (PO4 )2 (s) 3Ca+2 (aq) + 2PO4 −3 (aq)
The K expression for solubility product constant—called K sp —is written as:
K sp = [Ca+2 ] [C2 O4 −2 ]
K sp = [Pb+2 ] [I− ]2
K sp = [Ca+2 ]3 [PO4 −3 ]2
The solubility of the compound (in M units) can be calculated from the K sp data.
CaF2 (s) Ca+2 (aq) + 2F− (aq)
➤ Fill in the values.

Ca+2 + 2F−
Initial 0 0
+x +2x
At equilibrium x 2x
➤ Write the K sp expression.
K sp = [Ca+2 ] [F− ]2
192
UNIT II: ➤ Plug in value for K sp (found in the following table) and solve for x.
Chemical
Foundations of 4.0 × 10−11 = x(2x)2 = 4x3
Biological Systems x = [Ca+2 ] = 2.2 × 10−4 M
TABLE 6-2 Solubility Products of Some Slightly Soluble Ionic Compounds at 25 ◦ C
Compound Ksp
Aluminum hydroxide [Al(OH)3 ] 1.8 × 10−33

Barium carbonate (BaCO3 ) 8.1 × 10−9
Barium fluoride (BaF2 ) 1.7 × 10−6
Barium sulfate (BaSO4 ) 1.1 × 10−10
Bismuth sulfide (Bi2 S3 ) 1.6 × 10−72
Cadmium sulfide (CdS) 8.0 × 10−28
Calcium carbonate (CaCO3 ) 8.7 × 10−9
Calcium fluoride (CaF2 ) 4.0 × 10−11
Calcium hydroxide [Ca(OH)2 ] 8.0 × 10−6
Calcium phosphate [Ca3 (PO4 )2 ] 1.2 × 10−26
Chromium (III) hydroxide [Cr(OH)3 ] 3.0 × 10−29
Cobalt (II) sulfide (CoS) 4.0 × 10−21
Copper (I) bromide (CuBr) 4.2 × 10−8
Copper (I) iodide (CuI) 5.1 × 10−12
Copper (II) hydroxide [Cu(OH)2 ] 2.2 × 10−20
Copper (II) sulfide (CuS) 6.0 × 10−37
Iron (II) hydroxide [Fe(OH)2 ] 1.6 × 10−14
Iron (III) hydroxide [Fe(OH)3 ] 1.1 × 10−36
Iron (II) sulfide (FeS) 6.0 × 10−19
Lead (II) carbonate (PbCO3 ) 3.3 × 10−14
Lead (II) chloride (PbCl2 ) 2.4 × 10−4
Lead (II) chromate (PbCrO4 ) 2.0 × 10−14
Lead (II) fluoride (PbF2 ) 4.1 × 10−8
Lead (II) iodide (PbI2 ) 1.4 × 10−8
Lead (II) sulfide (PbS) 3.4 × 10−8
Magnesium carbonate (MgCO3 ) 4.0 × 10−5
Magnesium hydroxide [Mg(OH)2 ] 1.2 × 10−11
Manganese (II) sulfide (MnS) 3.0 × 10−14
Mercury (I) chloride (Hg2 Cl2 ) 3.5 × 10−18
Mercury (II) sulfide (HgS) 4.0 × 10−54
Nickel (II) sulfide (NiS) 1.4 × 10−24
Silver bromide (AgBr) 7.7 × 10−13
Silver carbonate (Ag2 CO3 ) 8.1 × 10−12
Silver chloride (AgCl) 1.6 × 10−10
Silver iodide (AgI) 8.3 × 10−17
Silver sulfate (Ag2 SO4 ) 1.4 × 10−5
Silver sulfide (Ag2 S) 6.0 × 10−51
Strontium carbonate (SrCO3 ) 1.6 × 10−9
Strontium sulfate (SrSO4 ) 1.6 × 10−9
Tin (II) sulfide (SnS) 1.0 × 10−26
Zinc hydroxide [Zn(OH)2 ] 1.8 × 10−14
Zinc sulfide (ZnS) 3.0 × 10−23
Conversely, the K sp can be calculated using solubility data.

193
EXAMPLE: Calculate the K sp of lead (II) iodide if the solubility is 1.2 × 10−3 M. CHAPTER 6:
The Unique Nature
SOLUTION: The solubility equals x; therefore, x = 1.2 × 10−3 . of Water and
Its Solutions
PbI2 (s) Pb+2 (aq) + 2I− (aq)

Pb+2 + 2I−
Initial 0 0
+1.2 × 10−3 (x) +2.4 × 10−3 (2x)
At equilibrium +1.2 × 10−3 +2.4 × 10−3

K sp = [Pb+2 ] [I− ]2
➤ Plug in values and solve for K sp .
K sp = (1.2 × 10−3 ) (2.4 × 10−3 )2
K sp = 6.9 × 10−9
Common Ion Effect

When one of the ions is added to a solution at equilibrium, the equilibrium shifts to
remove the added ion; thus the solubility lessens and more precipitate forms.
EXAMPLE: Calculate the solubility of calcium oxalate in 0.15 M calcium chloride.

The equilibrium constant, K sp , is:
K sp = 2.3 × 10−9
SOLUTION:
CaC2 O4 (s) Ca+2 (aq) + C2 O4 −2 (aq)

Ca+2 + C2 O4 −2
Initial 0.15 0
+x +x
At equilibrium 0.15 + x x
K sp = [Ca+2 ] [C2 O4 −2 ]
194
UNIT II: ➤ Plug in values and solve for x.
Chemical
Foundations of 2.3 × 10−9 = (0.15)x
Biological Systems x = [C2 O4 −2 ] = 1.5 × 10−8 M
The common ion effect occurs when you add strong acid or strong base to a solu-
tion of weak acid or weak base at equilibrium. The added base or acid reacts to form
more of one of the components in equilibrium.
EXAMPLE: Calculate the concentration of acetate ion in a solution that is 0.10 M

HAc and 0.010 M HCl. The equilibrium constant, K a , is:
K a = 1.8 × 10−5
SOLUTION:

HAc (aq) H+ (aq) + Ac− (aq)

HAc H+ + Ac−
Initial 0.10 0.010 0
−x +x +x
At equilibrium 0.10 − x 0.010 + x x

➤ Write the K a expression.
[H+ ] [Ac− ]
Ka =
[HAc]
➤ Plug in values.
(0.010) x
1.8 × 10−5 =
0.10
➤ Solve for x.
x = [Ac− ] = 1.8 × 10−4 M
COMPLEX ION FORMATION

Many metal ions can accept electron pairs from other molecules (Lewis bases), causing
the metal ions to act as Lewis acids. When these metal ions accept these electron pairs,
a complex ion forms. Some examples are:
Ag+ (aq) + 2NH3 (aq) → Ag(NH3 )2+ (aq)

Cu2+ (aq) + 4CN− (aq) → Cu(CN)4 (aq)
2−
Cd2+ (aq) + 4Br− (aq) → CdBr4 (aq)

2−
195
Accompanying these complexes are equilibrium constants of formation, or forma- CHAPTER 6:
tion constants, K f . The greater the value of K f , the more stable the complex of ions will The Unique Nature
be in aqueous solution. of Water and
Its Solutions
COMPLEX IONS AND SOLUBILITY

The addition of a Lewis base can drive an equilibrium and allow a slightly soluble salt
to be more soluble. For example, AgCl will be only slightly soluble in water according
to the reaction:
AgCl (s) → Ag+ (aq) + Cl− (aq)
However, should an electron pair be introduced into the preceding reaction, the
equilibrium can be shifted toward the right. If cyanide ion were then added to the pre-
ceding reaction, CN− would bond to Ag+ to form the complex ion Ag(CN)−
2 . This com-
plex ion has an equilibrium constant of formation, which is on the order of 10 21 . The
cyanide ion does a terrific job of removing the silver ions from solution, driving the
reaction to the right and increasing the solubility of AgCl.
SOLUBILITY AND pH
Lowering the pH increases the solubility of basic ionic compounds. If you calculate
the solubility of a basic compound in pure water as a reference, you can compare the
solubility at a lower pH.
EXAMPLE: (Part I—Reference): Calculate the solubility of nickel (II) hydroxide in

pure water. The solubility constant, K sp , is:
K sp = 2.0 × 10−15
SOLUTION:
Ni(OH)2 (s) Ni+2 (aq) + 2OH− (aq)

Ni+2 + 2OH−
Initial 0 0
+x +2x
At equilibrium x 2x
K sp = [Ni+2 ] [OH− ]2
➤ Plug in values and solve for x.

2.0 × 10−15 = x(2x)2
x = [Ni+2 ] = 7.9 × 10−6 M
196
UNIT II: EXAMPLE: (Part II): Calculate the solubility of nickel (II) hydroxide at pH 8.
Chemical
SOLUTION:
Foundations of
Biological Systems ➤ The pOH = 6; therefore, [OH− ] = 1 × 10−6 M.
➤ Plug in values using this concentration of OH− .
2.0 × 10−15 = x(1 × 10−6 )2
x = [Ni+2 ] = 2 × 10−3 M
EXAMPLE: (Part III): What is the pH of a saturated solution of nickel (II)

hydroxide in pure water?
SOLUTION:
[OH− ] = 2x = 2(7.9 × 10−6 ) = 1.6 × 10−5 M

pOH = 4.8
pH = 9.2
This says that at any pH less than 9.2, the solubility is > 7.9 × 10−6 M, and as shown
previously, at pH 8, the solubility is 2 × 10−3 M.
ACID–BASE TITRATIONS
An acid–base titration is the addition of a quantity of base of known concentration,
using a burette, to a known volume of acid of unknown concentration, until the end-
point is reached. An indicator compound, such as phenolphthalein, is added so that
a color change occurs at the endpoint. At that point, an equivalent amount of base has
been added, and the volume that contains that amount is determined from the initial
and final volumes on the burette. The concentration of the acid solution can then be
calculated.
EXAMPLE: A 25.0-mL sample of HCl is titrated with 0.0750 M NaOH. The titration
requires 32.7 mL of base to reach the endpoint. Calculate the molarity of the HCl.
SOLUTION:
➤ Write the equation for the reaction.
HCl + NaOH → NaCl + H2 O
➤ The stoichiometry of HCl to NaOH is 1 : 1.

➤ Calculate the moles of base added in the titration.
(0.0750 M) (0.0327 L) = 0.00245 mole NaOH added
➤ Calculate the moles of acid in the solution.

(0.00245 mole base) (1 mole acid/1 mole base) = 0.00245 mole acid
➤ Calculate the molarity of the acid.

M = mole/L = 0.00245 mole/0.0250 L = 0.098 M acid
197
There are two major types of acid–base titrations. One is the addition of strong CHAPTER 6:
base to strong acid; the other is the addition of strong base to weak acid. The pH of the The Unique Nature
endpoint solution can be calculated for the second case. of Water and
Its Solutions
Addition of Strong Base to Strong Acid

➤ The initial pH is the pH of the strong acid solution.
[H+ ] = [HA]
➤ At the midpoint, calculate the moles of acid left.

➤ Then calculate the M of the acid solution.
➤ Calculate the pH at the midpoint.
➤ At the endpoint, the pH is 7, because the salt is neutral.
Addition of Strong Base to Weak Acid

➤ The initial pH is the pH of the weak acid solution.
K a = x2 /[HA]
x = [H+ ]
pH = − log [H+ ]
➤ At the midpoint, use the Henderson–Hasselbach equation after calculating the

molarity of each component.
[A− ]
pH = pK a + log where pK a = − log K a
[HA]
➤ At the endpoint, it's the pH of a basic salt solution.
➤ Calculate the molarity of the salt.
➤ Calculate the K b .
K b = x2 /[A− ]
x = [OH− ]
➤ Calculate pOH.
➤ Calculate pH.
EXAMPLE: A 25.0-mL sample of 0.0875 M acetic acid is titrated with 0.150 M NaOH.
Consider the following given values:
K a = 1.8 × 10−5 pK a = 4.74
SOLUTION:
➤ Calculate the pH of the initial acid solution.

HA (aq) H+ (aq) + A− (aq)
[H+ ] [A− ]
Ka =
[HA]
198
UNIT II: 1.8 × 10−5 = x2 /0.0875
Chemical
x = [H+ ] = 1.25 × 10−3 M
Foundations of
Biological Systems pH = 2.9
➤ Calculate the pH at the point when 5.0 mL of base has been added.
(0.005 L) (0.150 M NaOH) = 7.5 × 10−4 mole base added
➤ Reacts with 7.5 × 10−4 mole acid.

(0.0250 L) (0.0875 M acid) = 2.188 × 10−3 mole acid initially
➤ Subtract 7.5 × 10−4 mole acid that is now gone to get:

1.438 × 10−3 mole acid in 30 mL = 0.0479 M acid, and
7.5 × 10−4 mole conj base in 30 mL = 0.0250 M base
➤ Plug into the Henderson–Hasselbach equation.

0.0250
pH = 4.74 + log
0.0479
pH = 4.5
➤ Calculate the pH at the endpoint of the titration.

Here, you have added 2.188 × 10−3 mole NaOH to completely neutralize
the initial amount of acid. This requires 2.188 × 10−3 mole/0.150 M = 0.0146 L
NaOH solution.
[A− ] = 2.188 × 10−3 mole/0.0396 L total = 0.055 M conj base
➤ Calculate K b = K w /K a = 5.6 × 10−10
K b = x2 /0.055 M = 5.6 × 10−10

x = [OH− ] = 5.5 × 10−6 M
pOH = 5.3
pH = 8.7
Indicators
The easiest way to tell the approximate pH value of a solution is via the use of an indi-
cator. Universal indicators are usually made from a blend of indicators and can have
more than six distinct colors to give more exact pH values. Other indicators, such as
litmus, have just two colors. When choosing an indicator for a titration, there is much
to consider.
Indicators such as phenolphthalein are useful during a titration because their
change in color tells you when the endpoint has been reached. The reaching of the
endpoint is the reaching of the equivalence point as well. Not all indicators turn color
at the same pH. This is why you need to pick an indicator with a pK that is close
199
to the equivalence point. For example, the equivalence point in a titration between CHAPTER 6:
NaOH and acetic acid is about 9.2. You would choose phenolphthalein for this reaction The Unique Nature
because it has a pK of 9.3. If you were to titrate a strong acid and a weak base, then of Water and
Its Solutions
methyl orange might be used as an indicator. The pK of this indicator is about 3.7,
and it changes color at a pH range of 3.1–4.4.
Neutralization
Neutralization is the process by which an acid and base are mixed together to form a
salt and water. A classic example is the reaction between HCl and NaOH to form NaCl
and H2 O. Because the three ionic compounds in the reaction are all completely soluble
electrolytes, the net ionic reaction for the neutralization of these substances will be:
H+ + OH− → H2 O
However, this is not the only type of neutralization that you can find. For example,
if you were to have an acid spill in the laboratory, you would use sodium bicarbonate
(NaHCO3 ) or sodium carbonate (Na2 CO3 ) to neutralize the spill. In these cases, the
acid is neutralized and carbon dioxide is formed. The equations for the reactions are:
HCl + NaHCO3 → NaCl + H2 O + CO2
2HCl + Na2 CO3 → 2NaCl + H2 O + CO2
Interpretation of Titration Curves

As a base or acid is titrated, the pH can be measured and plotted to form a titration
curve. In general, there are three more common shapes to be familiar with and one
that is less popular. In Figure 6-2, you can see the titration curve of a strong acid and a
strong base. As the strong base is titrated with the strong acid, the pH for the most part
stays relatively high until the equivalence point is reached. At the equivalence point,
the slope will be the steepest and the pH will be 7.
When a weak base is titrated with a strong acid, the pH will start at a lower basic
value and the endpoint will occur at a pH that is on the acidic side of the pH scale. The
opposite will occur when a strong base is titrated with a weak acid; the pH will start
very basic and the pH at the equivalence point will be in the basic range.
One more case to consider is when a diprotic or polyprotic acid is involved (see
Figure 6-3.). In the case of acids such as H2 CO3 or H3 PO4 , the curves will have more
than one equivalence point. Consider the titration of 25 mL of 0.100 M H2 CO3 with
0.100 M NaOH. The pH starts low as there is just acid present. When the first H+ ion is
completely removed from the acid, you have the first equivalence point, which takes
place after 25 mL of base are added. Now the base is titrating against the HCO−
3 . The
second equivalence point at 50 mL of base added shows another equivalence point
and a steep part of the curve. This shows the complete removal of the H+ ion from the
HCO−
2−
3 to form CO3 .
200
UNIT II:
Strong acid – strong base Strong acid – weak base
Chemical
pH pH
Foundations of
Biological Systems
7 7
Volume of acid added Volume of acid added
Weak acid – strong base Weak acid – weak base

pH pH
7 7
Volume of acid added Volume of acid added
FIGURE 6-2 Titration curves.
14
13
12
11
10
9
8
pH 7
6
5
4
3
2
1
0
0 10 20 30 40 50 60
mL 0.100 M NaOH added to 25 mL 0.100 M H2CO3
FIGURE 6-3 Titration curve when a diprotic or polyprotic acid is involved.
Oxidation–Reduction Reactions
Oxidation–reduction reactions, the third type of reaction in solution (next to precipi-
tation reactions and acid-base reactions), involve the transfer of one or more electrons
from one species in the reaction to another.
Any species that loses electrons is oxidized. Any species that gains electrons is
reduced. Oxidation and reduction can be tracked using the oxidation number of each
201
atom. Each atom in a formula has an oxidation number. It is similar to a charge; for CHAPTER 6:
simple ions, the charge and the oxidation number are the same. For atoms of an ele- The Unique Nature
ment, the oxidation number is always zero. of Water and
Its Solutions
RULES FOR OXIDATION NUMBERS

➤ The oxidation number of an atom in a pure element is zero.
➤ The oxidation number of a simple ion is the same as its charge.
➤ The oxidation number of oxygen is usually −2, except in peroxides, where it is −1.
➤ The oxidation number of hydrogen in a covalent compound is +1 unless it is
bonded to boron, where it is −1.
➤ The oxidation number of hydrogen in an ionic compound is −1.
➤ The oxidation number of fluorine is always −1.
➤ The sum of all the oxidation numbers in a neutral compound is always zero.
When the oxidation number of an atom decreases from one side of the equation to
the other side, that atom is reduced. If an oxidation number increases, that atom is
oxidized.
EXAMPLE: State which atom is oxidized and which is reduced in the following
equation:
Fe + Cu+2 → Fe+2 + Cu
SOLUTION:
1. Because Fe is an element, its oxidation number is 0.

2. Because Cu+2 is a simple ion, its oxidation number is +2.
3. Fe+2 is a simple ion; its oxidation number is +2.
4. Cu is an element; its oxidation number is 0.
5. Therefore, Fe is going from 0 to +2; Fe is being oxidized.
6. Cu is going from +2 to 0; Cu is reduced.
EXAMPLE: Try another problem. Which atom is oxidized and which is reduced?
2Sb + 3Cl2 → 2SbCl3
SOLUTION:
1. Because Sb is an element; its oxidation number is 0.

2. Because Cl2 is an element; its oxidation number of each Cl is 0.
3. Sb in SbCl3 is the ion Sb+3 ; oxidation number +3.
4. Cl in SbCl3 is the ion Cl−1 ; oxidation number −1.
5. Therefore,
Sb0 → Sb+3 oxidation

Cl0 → Cl−1 reduction
202
UNIT II: COMMON TYPES OF OXIDATION–REDUCTION REACTIONS
Chemical
Foundations of A few of the more common classifications of oxidation–reduction reactions are
Biological Systems combination reactions, decomposition reactions, single displacement reactions, and
combustion reactions.
A combination reaction occurs when two substances combine to form a third
substance.
CaO (s) + SO2 (g) → CaSO3 (s)
A decomposition reaction occurs when a single substance decomposes to two or

more substances.
2KClO3 → 2KCl + 3O2
A single displacement reaction occurs when an element reacts with an ionic

compound and replaces the cation in the compound. The original cation becomes an
element.
Cu + 2AgNO3 → 2Ag + Cu(NO3 )2
A combustion reaction occurs when a substance reacts with oxygen to produce

one or more oxides.
4Fe + 3O2 → 2Fe2 O3
OXIDATION–REDUCTION TITRATIONS
Oxidation–reduction titration typically does not require an indicator compound to be
added, because there is often an automatic color change on reaction.
EXAMPLE: A 25.0 mL sample of MnO4 − is titrated with 0.0485 M I− solution. To

reach the endpoint, 18.7 mL of the I− solution is required. Calculate the molarity
of the MnO4 − solution. The balanced equation is:
10I− + 16H+ + 2MnO4 − → 5I2 + 2Mn+2 + 8H2 O
➤ Calculate the moles of I− added.

(0.0485 mole/L) (0.0187 L) = 9.07 × 10−4 mole I− added
➤ Calculate the moles of MnO4 − .

(9.07 × 10−4 mole I− ) (2 mole MnO4 − /10 mole I− )
= 1.81 × 10−4 mole MnO4 −
➤ Calculate the molarity of MnO4 − .

M = 1.81 × 10−4 mole/0.0250 L = 0.00726 M MnO4 −

Chemical Foundations of Biological Systems

Uploaded by

Copyright:

Available Formats

Chemical Foundations of Biological Systems

Uploaded by

Document Information

Original Description:

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Chemical Foundations of Biological Systems

Uploaded by

Copyright:

Available Formats

MCAT-3200184 book November 13, 2015 15:28 MHID: 1-25-958837-8 ISBN: 1-25-958837-2

Foundational Concept: The principles that govern chemical interactions and

CHAPTER 6 The Unique Nature of Water and Its Solutions

The Unique Nature

Read This Chapter to Learn About

Brønsted–Lowry Definition of Acids and Bases

TYPES OF ACID–BASE REACTIONS

HCl + KOH → KCl + H2 O KCl is neutral.

HCl + NH4 OH → NH4 Cl + H2 O NH4 Cl is acidic.

The pH Scale CHAPTER 6:

Writing the K expression,

K w = [H+ ] [OH− ] = 1 × 10−14

[H+ ] = [OH− ] = 1 × 10−7 M

When [H+ ] = 1 × 10−3 M, the pH = 3; and when [OH− ] = 1 × 10−11 M, the

EXAMPLE: Calculate the pH if [H+ ] is 3.5 × 10−5 M.

➤ Because the exponent is −5, the pH is near 5.

EXAMPLE: Calculate [H+ ] when pH = 8.4.

EXAMPLE: Calculate [OH− ] when pH = 10.6.

Conjugate Acids and Bases

(ammonia) + (water) → (ammonium ion) + (hydroxide ion)

Strong Acids and Bases

HCl (aq) → H+ (aq) + Cl− (aq)

KOH (aq) → K+ (aq) + OH− (aq)

Ba(OH)2 (aq) → Ba2+ (aq) + 2 OH− (aq)

There is no equilibrium here; stoichiometry suffices to determine [OH− ] and, thus,

For Ba(OH)2 , the base concentration is half of the hydroxide concentration.

➤ [KOH] = [OH− ] = 0.065 M.

EXAMPLE: Calculate the pH of 0.065 M Ba(OH)2 . This is a strong base with 1 : 2

Weak Acids and Bases

HA (aq) H+ (aq) + A− (aq)

➤ Write the equation.

➤ Fill in the table.

➤ Calculate the pH.

EXAMPLE: Calculate the pH of 0.065 M NH3 . In this example, K b = 1.8 × 10−5 .

SOLUTION: This is a weak base; there are certain steps to follow.

➤ Write the equation.

➤ Fill in the table.

➤ Calculate the pOH.

➤ Calculate the pH.

➤ Carbonic acid has 2 protons (both weak):

➤ For the removal of the second proton,

➤ Removal of first proton,

H3 PO4 H+ + H2 PO4 −1 K a1 = 6.9 ×10−3

➤ Removal of second proton,

H2 PO4 −1 H+ + HPO4 −2 K a2 = 6.2 × 10−8

➤ Removal of third proton,

HPO4 −2 H+ + PO4 −3 K a3 = 4.8 × 10−13

pH OF A POLYPROTIC ACID SOLUTION

SALTS OF POLYPROTIC ACIDS

HCO3 −1 + H2 O OH− + H2 CO3 K b1 = 2.3 × 10−8

CO3 −2 + H2 O OH− + HCO3 −1 K b2 = 2.1 × 10−4

There are three salts of phosphoric acid:

H2 PO4 −1 + H2 O OH− + H3 PO4 K b1 = 1.4 × 10−12

➤ Calculate the pH.

EXAMPLE: Calculate the pH of 0.0165 M sodium hydrogen phosphate.

➤ Calculate pOH and pH.

acid + base → salt + H2 O

Strong acid + Strong base −→ Neutral salt pH = 7

Strong acid + Weak base −−→ Acidic salt pH < 7