acids dissociate and release H+ ions in aqueous solutions
alkalis dissociate and release OH- ions in aqueous solutions
H+ ions are neutralised by OH- ions to form water
H+ (aq) + OH- (aq)—> H2O (l)
An alkali is a soluble base
HCl —> H+ (aq) + Cl (aq)
HCl (aq) and Cl- (aq) are called a conjugate acid base pair
In the forward direction, HCl releases a proton to form its conjugate base Cl-
In the reverse direction Cl- accepts a proton to form its conjugate acid HCl
HCl + OH- -> H2O + Cl-
HCl is an acid as it donates H+
OH- is a base as it accepts H+
Monobasic acids —>An acid that contains only one hydrogen atom that can be replaced in an acid base reaction
Dibasic acid —> An acid that has two acidic hydrogen atoms in its molecule
Tribasic acid —> A substance that produces three hydrogen ions per molecule of the acid, when it gets completely dissociated in water
acid + metal —> salt + hydrogen
acid + carbonate —> salt + water + carbon dioxide
acid + base —> salt + water
acid + alkali –> salt + water
the pH scale:
pH less than 7 shows increasing acidity
pH greater than 7 shows increasing alkalinity
pH 7 is neutral
pH - a logarithmic scale:
A low value of [H+ (aq) ] matches a high value of pH
A high value of [H+(aq)] matches a low value of pH
pH = -log[H+ (aq)]
[H+ (aq)] = 10^-pH
Calculating the pH of strong acids:
In aqueous solutions, a strong monobasic acid, HA completely dissociates
HA (aq) —> H+ (aq) + A- (aq)
For a strong acid, [H+ (aq)] is equal to the concentration of the acid, [HA (aq)]
The pH of a strong acid can be calculated directly from the concentration of the acid
The ionic product of water:
Kw = [H+][OH-]
As temperature increases, the equation moves right to oppose the increase in temperature therefore [H+] and [OH-] increases
Kw increases and therefore pH decreases
However, the water is still neutral as [H+] = [OH-]
Kw = [H+]^2
Neutral --> [H+] = [OH-]
Dilution of strong base:
concentration x old volume / new volume
[H+] = Kw / [OH-]
pH = -log( Kw/ [OH-] )
Calculating pH - weak acids:
Can't be calculated by just knowing the concentration
Need to know the original concentration & the extent of the ionisation
The extent of the ionisation is given by Ka. The dissociation constant for a weak acid
CH3CO2H --> CH3CO2- + H+
HA --> A- + H+
Ka = [H+][A-] / [HA]
each acid has its own Ka
The bigger the Ka (more dissociated) - the less weak the acid
pKa:
pKa = -log(Ka)
Ka = 10^-pKa
For pKa, the smaller the number the stronger the acid
Assumption 1: [HA] at equilibrium is presumed to be the same as the original concentration. This is more of a problem for weak acids because [HA] will differ more
Assumption 2: [A-] = [H+]
A strong acid HA completely dissociates : [H+] = [HA]
A weak acid HA partially dissociates: [H+] doesn't equal [HA]
[H+] depends on:
the concentration of the acid
the acid dissociation constant Ka
Determination of Ka:
Experimentally the Ka for a weak acid can be determined by
preparing a standard solution of weak acid of known concentration
measuring the pH of the standard solution using a pH meter
Approximation 1: The dissociation of water is negligible
Approximation 2: The concentration of acids is much greater than the H+ concentration at equilibrium
Water ionises very slightly acting as both an acid and as a base
H2O --> H+(aq) + OH-(aq)
Ka = [H+(aq)][OH- (aq)] / [H2O(l)]
Kw is called the ionic product of water - the ions in water ( H+ and OH-) multiplied together
Kw = [H+ (aq)][OH-(aq)]
Kw varies with temperature
Kw = 1.00 x 10^-14 mol^2dm^-6
On dissociation, water is neutral - it produces the same number of H+ and OH- ions
[H+(aq)] = [OH-(aq)]
Kw is essentially an equilibrium constant that controls the concentration of H+ and OH- in aqueous solutions
A solution is acidic when [H+(aq)] > [OH-(aq)]
A solution is neutral when [H+(aq)] = [OH-(aq)]
A solution is alkaline when [H+(aq)] < [OH-(aq)]
A strong base is an alkali that completely dissociates in solution
NaOH (aq) --> Na+ (aq) + OH-(aq)
NaOH is a monobasic base as each mole of NaOH releases one mole of OH- ions
The pH of a strong base can be calculated from:
the concentration of the base
the ionic product of water Kw
Buffer solution --> solutions which resist changes in pH when small quantities of acid or alkali are added.
Uses of buffer solutions:
Standardising pH meters
Buffering biological systems
Maintaining the pH of shampoos
The weak acid, HA, removes added alkali
The conjugate base, A-, removes added acid
Making a buffer:
Add salt directly
Add approximately half of the mole of strong acid - leaving the acid in excess
Action of the buffer solution:
The conjugate acid-base pair, HA / A- in an acid buffer solution controls the pH
HA --> H+ + A-
The control of pH can be explained in terms of shifts in the equilibrium position using Le Chateliers principle
Conjugate base removes added acids:
On addition of an acid H+
[H+] increases
H+ ions react with the conjugate base A-
The equilibrium position shifts to the left, removing most of the H+ ions
Weak acid removes added alkali:
on addition of an alkali, OH-
[OH-] increases
The small concentration of H+ ions reacts with the OH- ions
HA dissociates, shifting the equilibrium position to the right to restore most of H+ ions
A buffer is most effective at removing either added acid or alkali when there are equal concentrations of the weak acid and its conjugate base
When [HA] = [A-]:
the pH of the buffer solution is the same as the pKa value of HA
the operating pH is typically over about 2 pH units, centered at the pH of the pKa value
the ratio of the concentrations of the weak acid and its conjugate base can then be adjusted to fine-tune the pH of the buffer solution
Buffers in blood:
Human blood contains a buffer of carbonic acid (H2CO3) & bicarbonate anion (HCO3-) in order to maintain blood pH between 7.35 & 7.45
CO2 is an important component of the blood buffer in regulation in the body
The effect of this can be important when the human body is subjected to strenuous conditions