Why is a logarithmic scale used for the pH scale?
Logarithmic scale:
Logarithms to the base 10
log10 10^x = x
For Example:
log10 10^3 =3
The pH scale
Low pH = high [H+(aq)]
High pH = low [H+(aq)]
A pH increase in 1 represents a 10 fold decrease in [H+(aq)]
Define:
pH = -log10[H+(aq)]
[H+] = 10^-pH
Calculating pH when solution is diluted
E.g
Halving the concentration of a STRONG acid increases its pH by 0.30
The STRENGTH of acids
The EXTENT to which it dissociates into H+(aq) and A-(aq) ions
STRONG Acids:
FULLY DISSCOIATE in aqueous solution
HA(aq) — H+(aq) + A-(aq)
WEAK Acids:
PARTIALLY DISSOCIATE in aqueous solution
HA(aq) (reversible sign) H+(aq) + A-(aq)
pH & [H+] of STRONG ACIDS
pH = -log10[H+(aq)]
[H+(aq)] = 10^-pH
pH & [H+] of WEAK ACIDS
[H+] = square root of (Ka x [HA])
pH = -log10[H+]
WEAK ACID:
Why is concentration in mol dm-3 not used to determine pH?
Not ALL the acid dissociates
pKa = -log10Ka
Ka = 10^-pKa
WEAK ACID:
Acid dissociation constant, Ka
Indicates the extent of acid dissociation
Ka = [products] / [reactants]
= [H+][A-] / [HA] = mol dm-3
LARGE Ka:
- large amount of dissociation
- [product] is high compared to [reactant]
- STRONGER WEAK ACID
SMALL Ka:
- small amount of dissociation
- [reactants] is high compared with [products]
- WEAKER ACID
WEAK ACID:
What is the Ka equation simplified to?
2 APPROXIMATIONS made
Ka = [H+]^2 equilibrium /[HA] start
1) [H+] = [A-] at equilibrium
2) [HA] at eqm = [HA] undissociated
WEAK ACID:
First approximation & its validity
(explained)
The approximation breaks down when the acid is either very strong or very dilute
WEAK ACID:
Second approximation & its validity
(explained)
INVALID FOR:
The equilibrium in Water
Hydronium ion, H3O+(aq) ~ very strong acid
Hydroxide ion, OH-(aq) ~ very strong base
H2O(l) + H2O(l) (reversible sign) H3O+(aq) + OH-(aq)
simplifies to:
H2O(l) (reversible sign) H+(aq) + OH-(aq)
Kw
Kw = [H+(aq)][OH-(aq)]
units: mol2 dm-6
pH of water
At 25 degrees, water has a pH of 7:
[H+(aq)] = 10-pH = 10-7 mol dm-3
The ionisation of water leads to a 1:1 molar ratio of H+ to OH- so:[OH-(aq)] = [H+(aq)]
Hence, 25 degrees:
[OH-] = 10-7 mol dm-3
Kw = [H+][OH-]
= 1x10-14 mol2 dm-6 at 25 degrees
Define the ionic product of water, include its value and units at 25 degrees
Kw = [H+(aq)][OH-(aq)]
= 1.00 x 10-14 mol 2 dm-6 at 25 degrees
Relationship between pKw & Kw
pKw = -log10Kw
What is the value of pKw at 25 degrees?
pKw = -log10Kw
= - log(1x10-14)
= 14
The relationship between [H+] & [OH-]
Kw = [H+][OH-]
= [H+]^2
= 1.00x10-14 mol2 dm-6 at 25 degrees
Kw = [H+][OH-]
10-14 = 10-8 x [OH-]
[OH-] = 10-6 mol dm-3
Indices of [H+] & [OH-] adds up to -14 for integer pH value
Working out pH of STRONG BASES
TWO METHODS
Kw:
[H+] = Kw / [OH-]
pH = -log10[H+]
pOH:
pOH = -log10[OH-]
pH = 14 - pOH
Working out pH of STRONG BASES
Method 1 ~ Kw
Kw = [H+][OH-]
[H+] = Kw/ [OH-]
= 1.00 x 10-14 / [OH-]
pH = -log [H+]
Working out pH of STRONG BASES
Method 2 ~ pOH
pOH = -log10[OH-]
pH + pOH =14
pH = 14 - pOH
Why are pKa values used instead of Ka values when comparing the strength of acids?
Easier to compare because they do not have:
(unlike Ka values)