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+ (KSP)
Salts of strong base and strong acid Acids: Liberates H2 on reacting with metals
cC + dD
aA neutral solution and does not undergo hy- Turns blue litumus into red
drolysis. eg. naCl, KCl Base: Taste bitter and feel soapy
K sp = [C] c [D] d Salt of weak base and Strong Acid
Turns red litmus into blue
Ionic product Kw H 1
of water Kh = ; p = [pK 2 − pK b − log c]
Kb 2
Salt of weak Acid and weak base Acidic ⇒ [H 3 O + ] > [OH− ]
+ −
H 3 O + OH
2H 2 O
Kw 1 Basic ⇒ [H 3 O + ] < [OH− ]
Kh = ; p H = [pK w − pK a − pK b ]
K w = [H 3 O + ][OH− ] = 1 × 10−14 M 2 Ka × Kb 2 Neutral ⇒ [H 3 O + ] = [OH− ]
∴ [OH− ] = [H+ ] = 10−7 M @ 298 K
B
pK w = pK a + pK b = 14
UILI RI
Q
Factor's of reaction
UM
Ostwald's Dilution Law
Le Chatlier's Principle
E
Effect of concentration change
Applicable for weak K electrlytes concentration →, equilibrium shift
Direction of
K forward.
∴ K c = Cα 2 or α = c reaction
C Effect of pressure change equilibrium
So, α =
1
orα ∝ v Qc < Kc will shift in the direction having
smaller number of moles.
c Reaction goes
Where V is the volume of solution Effect of temperature change
from left to right
at infinite dilution For exothermic → low temperature
Qc < Kc favors formation of reactants.
Reaction goes from For Endothermic → High temperature
right to left favors formation of products.
Qc = Kc Effect of inert gas → No change
Law of chemical Equilibrium No net reaction Effect of catalyst → No change
occurs
Equilibrium Law
Relation between equilibrium
aA + bB
cC + dD constant ckp + kc Definition
[C] C [D] d
Kc = a 6
K p = K c (RT)∆ng Equilibrium set up in a
physical process like
[A] [B] Chemical reaction reach a
evaporation of water
state of dynamic equilibrium etc.
Here Kc is equilibrium constant
in which the rate of forward
(s)
(l) Chemical
reaction and reaction are
(l)
(g)
same and there is no net
(g)
(s) Equilibrium attained in
PH Concept charge in composition
a chemical reaction
Gibb's energy
3H 2 + N 2
2NH 3
∆G = RT ln K p H = − log[H+ ] Homogeneous Hetrogeneous
∆G = -ve, spontaneous reaction H + Possible only in a closed
p = − log[H 3 O ]
Reaction proceeds forward. system.
∆G = +ve, Non spontaneous 1 Reactant and product Reactant and
for weak acid → p H = (C K − log c) are in same phase product are in Both reaction occur at
reation 2 p a different phase same rate
Reaction proceeds backward
All measurable property
∆G = zero, equilibrium achieved remains constant