1120 acid base

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    • according to the arrhenius theory, an acid dissociates in water to give H+
    • according to the arrhenius theory, a base dissociates in water to give OH-
    • limitations of arrhenius theory
      • solvent can only be water
      • cannot explain acid-base behaviour in non aqueous solution
      • cannot why all salts are neutral
    • according to the bronsted lowry theory, an acid is a proton donor
    • according to the bronsted lowry theory, a base is a proton acceptor
    • a bronsted base must have lone pair electrons
    • according to the lewis theory, an acid is an electron acceptor
    • according to the lewis theory, a base is an electron donor
    • if water is pure and at 25 ºC ,
      [H3O+ ] = [OH− ] = 1 x 10^-7 M
      Kw = [H3O+ ][OH− ] = 1 x 10^-14 M
    • pH = -log[H+]
    • pOH = -log[OH− ]
    • at 25ºC, pKw = pH + pOH = 14
    • Ka is the acid ionisation constant
    • Kb is the base ionisation constant
    • strong acid/base has a large ionising constant (much larger than 1)
    • weak acid/base has a small ionising constant (much smaller than 1)
    • Ka= [H+][A-]/[HA]
    • Kb= [BH+][OH-]/[B]
    • the stronger the acid, the weaker its conjugate base
    • the stronger the acid, the larger its Ka = the smaller its pKa
    • the stronger the base, the larger its Kb = the smaller its pKb
    • The percent ionization of a weak acid/base increases when the solution becomes more dilute.
    • % ionisation = [H+] / Initial [HA] and then times 100%
    • percent ionization depends on:
      1. Initial molarity
      2. ionization constant
    • K <<< 1 = backward favoured
    • K >>> 1 = forward favoured
    • K = 1 = equilibrium
    • Why does diluting the solution favour ionisation?
      Concentration is given by mole/volume.
      If volume increases, it means that concentration will decrease.
      Concerning Ka = [H+][A-]/[HA] , the number of moles of ions in this equation must increase to maintain the constant Ka. (constant = unchanged)
      Therefore this causes the equilibrium to shift to the right / product side, favouring ionisation
    • contribution of self-ionization of water to pH can be ignored unless the solution is extremely dilute
    • If the [H+] from the compound is greater than 1 x 10^-5 M, ignore self ionization of water
    • Polyprotic acids are acids with more than one ionizable proton (can donate multiple H+).
    • Each ionisation of H+ of a polyprotic acid has its own Ka value
    • H3PO4 is a triprotic acid
    • Ka3 < Ka2 < Ka1
      because it is more difficult to remove a proton from a more negatively charged species / weaker acid
    • Phosphoric Acid H3PO4 is a weak acid
    • Ka (acid) x Kb (its conjugate base) = Kw
    • Kb (base) x Ka (its conjugate acid) = Kw (constant)
    • In a conjugate acid base pair, larger Ka means a smaller Kb
    • In a conjugate acid base pair, larger Kb means a smaller Ka
    • When salt is dissolved in water, any pH change is caused by hydrolysis reaction
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