Acids, Bases and Buffers Flashcards
What is a Bronsted-Lowry acid?
A proton donor
What is a Bronsted-Lowry base?
A proton acceptor. (Dissociates OH-)
What happens when you put a strong acid into water?
The acid donates its proton, which forms a covalent bond with the water, producing H30+ and a negative ion.
Eg: HCl + H20 —> H3O+ + Cl-
(water can act as both an acid and base)
Why is water both an acid and base?
HCl + H2O —> H3O+ + Cl-
H30+ + Cl- —> HCl + H2O
Water accepts protons from stonger acids (base) and donates protons and donates a proton to the Cl- (acid)
(water can act as both an acid and base)
What are conjugate acid-base pairs?
Where both species in a reversible reaction act as both a base and acid.
Eg: CH3COOH (aq)+H2O (l)⇌CH3COO- (aq) +H3O+ (aq)
HCl(aq)+ H2O(l)⇌H3O+(aq) + Cl-(aq)
Give an example of a monobasic, dibasic, and tribasic acid.
HCl, H2S04, H3PO4
What is Ka? Give its expression
Acid dissociation constant, useful for weak acids as they don’t fully dissociate.
Ka = [H+][A-] / [HA]
HA⇌ H+ + A-
[H+] is the concentration of hydrogen ions, [A-] is the concentration of the conjugate base, [HA] is the concentration of the acid
How do you find pH from [H+]
pH= -log[H+]
How do you find [H+] from pH?
[H+]= 10^-pH
What is kw?
The acid dissociation constant of water multiplied by water concentration = ionic product of water = Kw.
kc = [H+] [OH-] / [H2O]. Because the concentration of water is constant:
kc = [H2O] = [H+] [OH-]
Kw = [H+] [OH-] = 1x10^-14 mol2 dm-6 AT 298K
What can be Kw used for?
Any aqueous solution. So the product oh [H+] [OH-] must be 1x10^-14 mol2 d m-6
How do you find the pH of strong bases?
[OH-] = base concentration (when monoprotic).
Insert into kw equation and rearrange for [H+].
[H+] = 1x10^-14 / [OH-]
Insert [H+] into pH=-log[H+]
What is ka in weak acids and explain why.
ka = [H+]^2 / [HA]
This is because weak acids partially dissociate so the concentration of H+ will be equal to conjugate base concentration (when the acid is all that is in solution).
What does a very small ka indicate about ewuilibrium posotion and acid strength.
The equilibrium is far to the left so the acid must be weak due to lack of dissociation into the conjugate base and protons.
What are the two assumptions made when using ka to find pH of weak acids?
That the concentration of H+ and conjugate base are the same.
That the concentration of the associated acid stays the same, or barely changes.
(As ka increases, more H+ is dissociated so the second assumption becomes less true)
So, ka is only useful for weak acids.