The basic enthalpy of neutralisation is -57.6kj/mol
In practical situations, enthalpy of neutralisation is never exact as H+ and OH- cannot exist on their own
Breaking bonds in acids such as HCN can alter the enthalpy of neutralisation
A Bronsted-Lowry acid is a substance that can donate a proton
A Bronsted-Lowry base is a substance that can accept a proton
Kw = [H+][OH-]
The Kw expression can be used to calculate [H+] if we know the [OH-] and vice versa
Kw is 1x10^-14 so pKw is 14
p infront of something mean -log10 of that thing
When finding the pH of water, square root Kw as the concentration of H+ and OH- is equal
When calculating pH of strong bases, use Kw and rearrange for [H+]
When calculating pH of weak acids, make 2 assumptions:
[H+] = [A-] because they have disassociated at a 1:1 ration
[HA] at equilibrium = [HA] initial as amount of acid disassociation is small
When calculating pH of weak acids, at half the neutralisation volume [HA]=[A-] and pH=pKa
pH of a diluted strong acid:
[H+]=[H+](old) x old volume/new volume
A basic buffer is made from a weak base and the salt of that base
A weak base must have a strong conjugate acid
Buffer solutions contain a resevoir of HA and A- ions
If small amounts of alkali are added to the buffer, the OH- ions react with H+ ions (from the weak acid) to form water. Because there is only a small amount of H+ ions (since the acid only slightly disassociates), equilibrium will shift to produce more H+ ions, lowering the pH
If a small amount of acid is added to the buffer solution, equilibrium will shift to produce more salt and the H+ ions will react with the reservoir A- ions
A buffer can be made from partially neutralising a weak acid
Calculating pH of a buffer:
Rearrange Ka for [H+]
Calculate moles of salt and weak acid
Using ratio, find which reactant is in excess and by how much