Q1. Zeroth Law
Assertion (A): If two systems are separately in thermal equilibrium with a third system, they are in thermal equilibrium with each other.
Reason (R): All systems in thermal equilibrium have the same temperature.
(1) A & R both true and R is correct explanation
(2) A & R both true but R is not correct explanation
(3) A true, R false
(4) A false, R true
Q2. First Law
Assertion (A): Internal energy of an isolated system remains constant.
Reason (R): Energy can neither be created nor destroyed, only converted from one form to another.
(1) A & R both true and R is correct explanation
(2) A & R both true but R is not correct explanation
(3) A true, R false
(4) A false, R true
Q3. Second Law
Assertion (A): Heat cannot spontaneously flow from a colder body to a hotter body.
Reason (R): Total entropy of an isolated system always increases for a spontaneous process.
(1) A & R both true and R is correct explanation
(2) A & R both true but R is not correct explanation
(3) A true, R false
(4) A false, R true
Q4. Third Law
Assertion (A): Entropy of a perfectly crystalline substance is zero at absolute zero temperature.
Reason (R): At absolute zero, only one microstate is possible.
(1) A & R both true and R is correct explanation
(2) A & R both true but R is not correct explanation
(3) A true, R false
(4) A false, R true
๐คฉ3โค1๐ณ1
โญ ๐๐๐ ๐ชEE (๐๐ก, ๐๐, ๐ ๐ ๐ฆ๐ง๐๐ฅ, ๐ ๐๐ & so on) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ข๐๐ ๐๐๐๐ง๐จ๐ฅ๐๐ฆ โ ๐จ๐ก๐๐ ๐ฌ + ๐๐ก ๐@๐ง๐ + ๐ฆ@๐ฉ@๐ + ๐ข๐ง๐๐๐ฅ ๐ง๐ข๐ฃ ๐ง๐๐๐๐๐๐ฅ๐ฆ
โญ ๐จ๐ก๐๐ ๐ฌ (๐ง๐ก๐ , ๐ฅ๐, ๐ฌ๐ฆ๐ฌ, ๐๐๐๐, ๐ฆ๐ง ๐ฆ๐๐ฅ, ๐๐ก๐ฆ๐๐ ๐๐๐ ๐ฆ๐๐ฅ & So On ) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ฆ@๐ฉ@๐ (๐๐ ๐ฆ๐๐ฅ, ๐๐ฆ๐๐๐ฆ๐ ๐๐๐๐ฃ๐๐ฌ๐ ๐ฆ๐๐ฅ, ๐ฃ๐๐ฅ๐ฉ๐๐ญ ๐๐๐๐ก, ๐ฉ๐
๐ฆ๐๐ฅ & ๐ฆ๐ข ๐ข๐ก) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐๐ข๐ฃ๐ฌ๐ฅ๐๐๐๐ง ๐๐๐๐๐จ๐ฃ ๐ข๐ ๐๐๐ ๐ข๐ ๐ง๐๐๐ฆ
โญ ๐ข๐๐ ๐๐๐๐ง๐จ๐ฅ๐๐ฆ โ ๐จ๐ก๐๐ ๐ฌ + ๐๐ก ๐@๐ง๐ + ๐ฆ@๐ฉ@๐ + ๐ข๐ง๐๐๐ฅ ๐ง๐ข๐ฃ ๐ง๐๐๐๐๐๐ฅ๐ฆ
โญ ๐จ๐ก๐๐ ๐ฌ (๐ง๐ก๐ , ๐ฅ๐, ๐ฌ๐ฆ๐ฌ, ๐๐๐๐, ๐ฆ๐ง ๐ฆ๐๐ฅ, ๐๐ก๐ฆ๐๐ ๐๐๐ ๐ฆ๐๐ฅ & So On ) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ฆ@๐ฉ@๐ (๐๐ ๐ฆ๐๐ฅ, ๐๐ฆ๐๐๐ฆ๐ ๐๐๐๐ฃ๐๐ฌ๐ ๐ฆ๐๐ฅ, ๐ฃ๐๐ฅ๐ฉ๐๐ญ ๐๐๐๐ก, ๐ฉ๐
๐ฆ๐๐ฅ & ๐ฆ๐ข ๐ข๐ก) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐๐ข๐ฃ๐ฌ๐ฅ๐๐๐๐ง ๐๐๐๐๐จ๐ฃ ๐ข๐ ๐๐๐ ๐ข๐ ๐ง๐๐๐ฆ
๐2๐1
Chemistry booster series
โญ ๐๐๐ ๐ชEE (๐๐ก, ๐๐, ๐ ๐ ๐ฆ๐ง๐๐ฅ, ๐ ๐๐ & so on) ๐ฎ๐ฌ๐ฎ๐ฒ โญ ๐ข๐๐ ๐๐๐๐ง๐จ๐ฅ๐๐ฆ โ ๐จ๐ก๐๐ ๐ฌ + ๐๐ก ๐@๐ง๐ + ๐ฆ@๐ฉ@๐ + ๐ข๐ง๐๐๐ฅ ๐ง๐ข๐ฃ ๐ง๐๐๐๐๐๐ฅ๐ฆ โญ ๐จ๐ก๐๐ ๐ฌ (๐ง๐ก๐ , ๐ฅ๐, ๐ฌ๐ฆ๐ฌ, ๐๐๐๐, ๐ฆ๐ง ๐ฆ๐๐ฅ, ๐๐ก๐ฆ๐๐ ๐๐๐ ๐ฆ๐๐ฅ & So On ) ๐ฎ๐ฌ๐ฎ๐ฒ โญ ๐ฆ@๐ฉ@๐ (๐๐ ๐ฆ๐๐ฅ, ๐๐ฆ๐๐๐ฆ๐ ๐๐๐๐ฃ๐๐ฌ๐ ๐ฆ๐๐ฅ, ๐ฃ๐๐ฅ๐ฉ๐๐ญ ๐๐๐๐ก, ๐ฉ๐ ๐ฆ๐๐ฅ & ๐ฆ๐ข ๐ข๐ก) ๐ฎ๐ฌ๐ฎ๐ฒ โญ ๐๐ข๐ฃ๐ฌ๐ฅ๐๐๐๐งโฆ
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๐1๐1๐ณ1
1๏ธโฃ #GIBBSFREEENERGY
โ๏ธ Thermodynamic state function
โ๏ธ Determines spontaneity of process
โ๏ธ Denoted by G
๐ Relation:
G = H โ TS
2๏ธโฃ #TERMSINFORMULA
โ๏ธ H โ Enthalpy
โ๏ธ T โ Absolute temperature (K)
โ๏ธ S โ Entropy
๐ Unit of G โ Joule
3๏ธโฃ #CHANGEINGIBBSENERGY
๐ Formula:
ฮG = ฮH โ TฮS
โ๏ธ Applies at constant T & P
4๏ธโฃ #SIGNIFICANCEOFฮG (VERY IMP )
โ๏ธ ฮG < 0 โ Spontaneous process
โ๏ธ ฮG = 0 โ Equilibrium
โ๏ธ ฮG > 0 โ Non-spontaneous
5๏ธโฃ #CASESBASEDONฮHANDฮS
โ๏ธ ฮH < 0 and ฮS > 0
Process spontaneous at all temperatures
โ๏ธ ฮH > 0 and ฮS < 0
Process non-spontaneous at all temperatures
โ๏ธ ฮH < 0 and ฮS < 0
Spontaneous at low temperature
โ๏ธ ฮH > 0 and ฮS > 0
Spontaneous at high temperature
6๏ธโฃ #TEMPERATUREEFFECT
โ๏ธ Increase in T increases importance of entropy term
โ๏ธ TฮS dominates at high temperature
7๏ธโฃ #GIBBSENERGYATEQUILIBRIUM
โ๏ธ At equilibrium:
ฮG = 0
๐ Relation with equilibrium constant:
ฮGยฐ = โRT ln K
8๏ธโฃ #STANDARDGIBBSFREEENERGY
โ๏ธ Measured at:
โ๏ธ 1 bar pressure
โ๏ธ 298 K temperature
๐ Formula:
ฮGยฐ = ฮHยฐ โ TฮSยฐ
9๏ธโฃ #REACTIONQUOTIENTRELATION
๐ Formula:
ฮG = ฮGยฐ + RT ln Q
โ๏ธ Q = reaction quotient
๐ At equilibrium Q = K
๐ #MAXIMUMWORKCONCEPT
โ๏ธ ฮG gives maximum non-expansion work
โ๏ธ Useful in electrochemistry
๐ Electrical work = โฮG
1๏ธโฃ1๏ธโฃ #GIBBSENERGYINELECTROCHEMISTRY
๐ Relation:
ฮGยฐ = โnFEยฐ
โ๏ธ n = number of electrons
โ๏ธ F = Faraday constant
โ๏ธ Eยฐ = standard emf
1๏ธโฃ2๏ธโฃ #UNITSOFฮG
โ๏ธ Joule
โ๏ธ kJ molโปยน (mostly used in chemistry)
1๏ธโฃ3๏ธโฃ #NEET
โ๏ธ ฮG decides feasibility, not rate
โ๏ธ Spontaneous โ fast
โ๏ธ ฮG depends on T, P & composition
โ๏ธ ฮG is state function
1๏ธโฃ4๏ธโฃ #ONELINEREVISION
โ๏ธ Gibbs free energy predicts spontaneity
โ๏ธ ฮG = 0 at equilibrium
โ๏ธ Negative ฮG โ feasible process
โ๏ธ ฮGยฐ related to K and Eยฐ
โ๏ธ Thermodynamic state function
โ๏ธ Determines spontaneity of process
โ๏ธ Denoted by G
๐ Relation:
G = H โ TS
2๏ธโฃ #TERMSINFORMULA
โ๏ธ H โ Enthalpy
โ๏ธ T โ Absolute temperature (K)
โ๏ธ S โ Entropy
๐ Unit of G โ Joule
3๏ธโฃ #CHANGEINGIBBSENERGY
๐ Formula:
ฮG = ฮH โ TฮS
โ๏ธ Applies at constant T & P
4๏ธโฃ #SIGNIFICANCEOFฮG (VERY IMP )
โ๏ธ ฮG < 0 โ Spontaneous process
โ๏ธ ฮG = 0 โ Equilibrium
โ๏ธ ฮG > 0 โ Non-spontaneous
5๏ธโฃ #CASESBASEDONฮHANDฮS
โ๏ธ ฮH < 0 and ฮS > 0
Process spontaneous at all temperatures
โ๏ธ ฮH > 0 and ฮS < 0
Process non-spontaneous at all temperatures
โ๏ธ ฮH < 0 and ฮS < 0
Spontaneous at low temperature
โ๏ธ ฮH > 0 and ฮS > 0
Spontaneous at high temperature
6๏ธโฃ #TEMPERATUREEFFECT
โ๏ธ Increase in T increases importance of entropy term
โ๏ธ TฮS dominates at high temperature
7๏ธโฃ #GIBBSENERGYATEQUILIBRIUM
โ๏ธ At equilibrium:
ฮG = 0
๐ Relation with equilibrium constant:
ฮGยฐ = โRT ln K
8๏ธโฃ #STANDARDGIBBSFREEENERGY
โ๏ธ Measured at:
โ๏ธ 1 bar pressure
โ๏ธ 298 K temperature
๐ Formula:
ฮGยฐ = ฮHยฐ โ TฮSยฐ
9๏ธโฃ #REACTIONQUOTIENTRELATION
๐ Formula:
ฮG = ฮGยฐ + RT ln Q
โ๏ธ Q = reaction quotient
๐ At equilibrium Q = K
๐ #MAXIMUMWORKCONCEPT
โ๏ธ ฮG gives maximum non-expansion work
โ๏ธ Useful in electrochemistry
๐ Electrical work = โฮG
1๏ธโฃ1๏ธโฃ #GIBBSENERGYINELECTROCHEMISTRY
๐ Relation:
ฮGยฐ = โnFEยฐ
โ๏ธ n = number of electrons
โ๏ธ F = Faraday constant
โ๏ธ Eยฐ = standard emf
1๏ธโฃ2๏ธโฃ #UNITSOFฮG
โ๏ธ Joule
โ๏ธ kJ molโปยน (mostly used in chemistry)
1๏ธโฃ3๏ธโฃ #NEET
โ๏ธ ฮG decides feasibility, not rate
โ๏ธ Spontaneous โ fast
โ๏ธ ฮG depends on T, P & composition
โ๏ธ ฮG is state function
1๏ธโฃ4๏ธโฃ #ONELINEREVISION
โ๏ธ Gibbs free energy predicts spontaneity
โ๏ธ ฮG = 0 at equilibrium
โ๏ธ Negative ฮG โ feasible process
โ๏ธ ฮGยฐ related to K and Eยฐ
๐ฅ2๐1๐1
โญ ๐๐๐ ๐ชEE ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ (๐๐ก, ๐๐, ๐ ๐ ๐ฆ๐ง๐๐ฅ, ๐ ๐๐ & so on) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ข๐๐ ๐๐๐๐ง๐จ๐ฅ๐๐ฆ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐โ ๐จ๐ก๐๐ ๐ฌ + ๐๐ก ๐@๐ง๐ + ๐ฆ@๐ฉ@๐ + ๐ข๐ง๐๐๐ฅ ๐ง๐ข๐ฃ ๐ง๐๐๐๐๐๐ฅ๐ฆ
โญ ๐จ๐ก๐๐ ๐ฌ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ (๐ง๐ก๐ , ๐ฅ๐, ๐ฌ๐ฆ๐ฌ, ๐๐๐๐, ๐ฆ๐ง ๐ฆ๐๐ฅ, ๐๐ก๐ฆ๐๐ ๐๐๐ ๐ฆ๐๐ฅ & So On ) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ฆ@๐ฉ@๐ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐(๐๐ ๐ฆ๐๐ฅ, ๐๐ฆ๐๐๐ฆ๐ ๐๐๐๐ฃ๐๐ฌ๐ ๐ฆ๐๐ฅ, ๐ฃ๐๐ฅ๐ฉ๐๐ญ ๐๐๐๐ก, ๐ฉ๐
๐ฆ๐๐ฅ & ๐ฆ๐ข ๐ข๐ก) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐๐ข๐ฃ๐ฌ๐ฅ๐๐๐๐ง ๐๐๐๐๐จ๐ฃ ๐ข๐ ๐๐๐๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ ๐ข๐ ๐ง๐๐๐ฆ
โญ ๐ข๐๐ ๐๐๐๐ง๐จ๐ฅ๐๐ฆ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐โ ๐จ๐ก๐๐ ๐ฌ + ๐๐ก ๐@๐ง๐ + ๐ฆ@๐ฉ@๐ + ๐ข๐ง๐๐๐ฅ ๐ง๐ข๐ฃ ๐ง๐๐๐๐๐๐ฅ๐ฆ
โญ ๐จ๐ก๐๐ ๐ฌ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ (๐ง๐ก๐ , ๐ฅ๐, ๐ฌ๐ฆ๐ฌ, ๐๐๐๐, ๐ฆ๐ง ๐ฆ๐๐ฅ, ๐๐ก๐ฆ๐๐ ๐๐๐ ๐ฆ๐๐ฅ & So On ) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ฆ@๐ฉ@๐ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐(๐๐ ๐ฆ๐๐ฅ, ๐๐ฆ๐๐๐ฆ๐ ๐๐๐๐ฃ๐๐ฌ๐ ๐ฆ๐๐ฅ, ๐ฃ๐๐ฅ๐ฉ๐๐ญ ๐๐๐๐ก, ๐ฉ๐
๐ฆ๐๐ฅ & ๐ฆ๐ข ๐ข๐ก) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐๐ข๐ฃ๐ฌ๐ฅ๐๐๐๐ง ๐๐๐๐๐จ๐ฃ ๐ข๐ ๐๐๐๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ ๐ข๐ ๐ง๐๐๐ฆ
โค1๐ฅ1๐1
Chemistry booster series
โญ ๐๐๐ ๐ชEE ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ (๐๐ก, ๐๐, ๐ ๐ ๐ฆ๐ง๐๐ฅ, ๐ ๐๐ & so on) ๐ฎ๐ฌ๐ฎ๐ฒ โญ ๐ข๐๐ ๐๐๐๐ง๐จ๐ฅ๐๐ฆ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐โ ๐จ๐ก๐๐ ๐ฌ + ๐๐ก ๐@๐ง๐ + ๐ฆ@๐ฉ@๐ + ๐ข๐ง๐๐๐ฅ ๐ง๐ข๐ฃ ๐ง๐๐๐๐๐๐ฅ๐ฆ โญ ๐จ๐ก๐๐ ๐ฌ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ (๐ง๐ก๐ , ๐ฅ๐, ๐ฌ๐ฆ๐ฌ, ๐๐๐๐, ๐ฆ๐ง ๐ฆ๐๐ฅ, ๐๐ก๐ฆ๐๐ ๐๐๐ ๐ฆ๐๐ฅ & So On ) ๐ฎ๐ฌ๐ฎ๐ฒ โญ ๐ฆ@๐ฉ@๐ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐(๐๐ ๐ฆ๐๐ฅ, ๐๐ฆ๐๐๐ฆ๐ ๐๐๐๐ฃ๐๐ฌ๐โฆ
Join kr lena all bcz in sbke full lec + crash course+ handwriting notes +short notes + test All in one milega
Haar batch ka even more then batch content
Haar batch ka even more then batch content
โค1๐คฉ1๐1
Q1.
Assertion (A): For a spontaneous process at constant temperature and pressure, ฮG is negative.
Reason (R): Spontaneous processes occur with decrease in Gibbs free energy.
Options:
(1) A & R true, R correct explanation
(2) A & R true, R not explanation
(3) A true, R false
(4) A false, R true
Q2.
Assertion (A): When ฮG = 0, the system is at equilibrium.
Reason (R): At equilibrium, forward and backward reaction rates are equal
Q3.
Assertion (A): A reaction with ฮH < 0 and ฮS < 0 is spontaneous at all temperatures.
Reason (R): Decrease in enthalpy always favours spontaneity.
Q5. (Numerical concept)
Assertion (A): If ฮH = โ40 kJ and ฮS = โ100 J Kโปยน, reaction is spontaneous at low temperature.
Reason (R): Negative ฮS disfavors spontaneity at high temperature
๐1๐1๐ณ1
โญ ๐๐๐ ๐ชEE ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ (๐๐ก, ๐๐, ๐ ๐ ๐ฆ๐ง๐๐ฅ, ๐ ๐๐ & so on) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ข๐๐ ๐๐๐๐ง๐จ๐ฅ๐๐ฆ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐โ ๐จ๐ก๐๐ ๐ฌ + ๐๐ก ๐@๐ง๐ + ๐ฆ@๐ฉ@๐ + ๐ข๐ง๐๐๐ฅ ๐ง๐ข๐ฃ ๐ง๐๐๐๐๐๐ฅ๐ฆ
โญ ๐จ๐ก๐๐ ๐ฌ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ (๐ง๐ก๐ , ๐ฅ๐, ๐ฌ๐ฆ๐ฌ, ๐๐๐๐, ๐ฆ๐ง ๐ฆ๐๐ฅ, ๐๐ก๐ฆ๐๐ ๐๐๐ ๐ฆ๐๐ฅ & So On ) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ฆ@๐ฉ@๐ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐(๐๐ ๐ฆ๐๐ฅ, ๐๐ฆ๐๐๐ฆ๐ ๐๐๐๐ฃ๐๐ฌ๐ ๐ฆ๐๐ฅ, ๐ฃ๐๐ฅ๐ฉ๐๐ญ ๐๐๐๐ก, ๐ฉ๐
๐ฆ๐๐ฅ & ๐ฆ๐ข ๐ข๐ก) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐๐ข๐ฃ๐ฌ๐ฅ๐๐๐๐ง ๐๐๐๐๐จ๐ฃ ๐ข๐ ๐๐๐๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ ๐ข๐ ๐ง๐๐๐ฆ
โญ ๐ข๐๐ ๐๐๐๐ง๐จ๐ฅ๐๐ฆ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐โ ๐จ๐ก๐๐ ๐ฌ + ๐๐ก ๐@๐ง๐ + ๐ฆ@๐ฉ@๐ + ๐ข๐ง๐๐๐ฅ ๐ง๐ข๐ฃ ๐ง๐๐๐๐๐๐ฅ๐ฆ
โญ ๐จ๐ก๐๐ ๐ฌ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ (๐ง๐ก๐ , ๐ฅ๐, ๐ฌ๐ฆ๐ฌ, ๐๐๐๐, ๐ฆ๐ง ๐ฆ๐๐ฅ, ๐๐ก๐ฆ๐๐ ๐๐๐ ๐ฆ๐๐ฅ & So On ) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐ฆ@๐ฉ@๐ ๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐(๐๐ ๐ฆ๐๐ฅ, ๐๐ฆ๐๐๐ฆ๐ ๐๐๐๐ฃ๐๐ฌ๐ ๐ฆ๐๐ฅ, ๐ฃ๐๐ฅ๐ฉ๐๐ญ ๐๐๐๐ก, ๐ฉ๐
๐ฆ๐๐ฅ & ๐ฆ๐ข ๐ข๐ก) ๐ฎ๐ฌ๐ฎ๐ฒ
โญ ๐๐ข๐ฃ๐ฌ๐ฅ๐๐๐๐ง ๐๐๐๐๐จ๐ฃ ๐ข๐ ๐๐๐๐๐ฅ๐๐๐ ๐๐ข๐ฅ๐๐ ๐ข๐ ๐ง๐๐๐ฆ
โค2๐ฅ1๐1
Chemistry booster series
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โคโ๐ฅ4โค2๐ฅฐ1
1๏ธโฃ #CHEMICALEQUILIBRIUM
โ๏ธ State where forward & reverse reactions occur at same rate
โ๏ธ Concentrations of reactants & products become constant
๐ Example:
Nโ + 3Hโ โ 2NHโ
2๏ธโฃ #EQUILIBRIUMCONSTANT (K)
โ๏ธ Ratio of product concentrations to reactant concentrations
โ๏ธ Each raised to power of stoichiometric coefficient
๐ General reaction:
aA + bB โ cC + dD
๐ Expression:
Kc = [C]แถ[D]แต / [A]แต[B]แต
3๏ธโฃ #TYPESOFEQUILIBRIUMCONSTANT
โ๏ธ Kc โ concentration based
โ๏ธ Kp โ partial pressure based
๐ Relation:
Kp = Kc(RT)โฟ
โ๏ธ n = moles of gaseous products โ moles of gaseous reactants
4๏ธโฃ #SIGNIFICANCEOFK
โ๏ธ Predicts extent of reaction
โ๏ธ Tells position of equilibrium
๐ Values:
โ๏ธ K โซ 1 โ Product favoured
โ๏ธ K โช 1 โ Reactant favoured
โ๏ธ K โ 1 โ Both present
5๏ธโฃ #REACTIONQUOTIENT (Q)
โ๏ธ Same expression as K
โ๏ธ Calculated at any stage of reaction
๐ Comparison:
โ๏ธ Q < K โ reaction proceeds forward
โ๏ธ Q > K โ reaction proceeds backward
โ๏ธ Q = K โ equilibrium
6๏ธโฃ #APPLICATION1DIRECTIONOFREACTION
โ๏ธ Compare Q with K
โ๏ธ Predict spontaneous direction
๐ Very important for numericals
7๏ธโฃ #APPLICATION2DEGREEOFDISSOCIATION
โ๏ธ Used for weak electrolytes
๐ Example:
HA โ Hโบ + Aโป
K = ฮฑยฒC / (1 โ ฮฑ)
โ๏ธ ฮฑ = degree of dissociation
โ๏ธ C = initial concentration
8๏ธโฃ #APPLICATION3IONIZATIONOFWEAKELECTROLYTES
โ๏ธ Acids & bases have small K value
๐ Example:
CHโCOOH โ Hโบ + CHโCOOโป
โ๏ธ Small K โ weak acid
9๏ธโฃ #APPLICATION4CALCULATIONOFCONCENTRATION
โ๏ธ Find unknown equilibrium concentration
โ๏ธ Used in ICE table method
๐ Steps:
โ๏ธ Initial concentration
โ๏ธ Change
โ๏ธ Equilibrium
๐ #APPLICATION5EFFECTOFCHANGINGCONDITIONS
โ๏ธ Temperature change affects K
โ๏ธ Concentration & pressure do NOT change K
๐ Only temperature changes K value
1๏ธโฃ1๏ธโฃ #EFFECTOFTEMPERATURE
โ๏ธ Endothermic reaction:
Temperature โ โ K โ
โ๏ธ Exothermic reaction:
Temperature โ โ K โ
1๏ธโฃ2๏ธโฃ #RELATIONWITHGIBBSFREEENERGY
๐ Formula:
ฮGยฐ = โRT ln K
โ๏ธ ฮGยฐ < 0 โ K > 1 (spontaneous)
โ๏ธ ฮGยฐ > 0 โ K < 1
1๏ธโฃ3๏ธโฃ #HETEROGENEOUSEQUILIBRIUM
โ๏ธ Solids & liquids not included in K
๐ Example:
CaCOโ(s) โ CaO(s) + COโ(g)
Kp = P(COโ)
1๏ธโฃ4๏ธโฃ #REVERSINGREACTION
โ๏ธ K(reverse) = 1 / K(forward)
1๏ธโฃ5๏ธโฃ #MULTIPLYINGREACTION
โ๏ธ If reaction multiplied by n
โ๏ธ New K = Kโฟ
1๏ธโฃ6๏ธโฃ #NEETโ ๏ธ
โ๏ธ K depends only on temperature
โ๏ธ Catalyst does not change K
โ๏ธ Pure solids not included
โ๏ธ Units of K depend on reaction
1๏ธโฃ7๏ธโฃ #ONELINEREVISION
โ๏ธ K predicts extent of reaction
โ๏ธ Q vs K gives direction
โ๏ธ Only temperature affects K
โ๏ธ KpโKc relation important
โ๏ธ State where forward & reverse reactions occur at same rate
โ๏ธ Concentrations of reactants & products become constant
๐ Example:
Nโ + 3Hโ โ 2NHโ
2๏ธโฃ #EQUILIBRIUMCONSTANT (K)
โ๏ธ Ratio of product concentrations to reactant concentrations
โ๏ธ Each raised to power of stoichiometric coefficient
๐ General reaction:
aA + bB โ cC + dD
๐ Expression:
Kc = [C]แถ[D]แต / [A]แต[B]แต
3๏ธโฃ #TYPESOFEQUILIBRIUMCONSTANT
โ๏ธ Kc โ concentration based
โ๏ธ Kp โ partial pressure based
๐ Relation:
Kp = Kc(RT)โฟ
โ๏ธ n = moles of gaseous products โ moles of gaseous reactants
4๏ธโฃ #SIGNIFICANCEOFK
โ๏ธ Predicts extent of reaction
โ๏ธ Tells position of equilibrium
๐ Values:
โ๏ธ K โซ 1 โ Product favoured
โ๏ธ K โช 1 โ Reactant favoured
โ๏ธ K โ 1 โ Both present
5๏ธโฃ #REACTIONQUOTIENT (Q)
โ๏ธ Same expression as K
โ๏ธ Calculated at any stage of reaction
๐ Comparison:
โ๏ธ Q < K โ reaction proceeds forward
โ๏ธ Q > K โ reaction proceeds backward
โ๏ธ Q = K โ equilibrium
6๏ธโฃ #APPLICATION1DIRECTIONOFREACTION
โ๏ธ Compare Q with K
โ๏ธ Predict spontaneous direction
๐ Very important for numericals
7๏ธโฃ #APPLICATION2DEGREEOFDISSOCIATION
โ๏ธ Used for weak electrolytes
๐ Example:
HA โ Hโบ + Aโป
K = ฮฑยฒC / (1 โ ฮฑ)
โ๏ธ ฮฑ = degree of dissociation
โ๏ธ C = initial concentration
8๏ธโฃ #APPLICATION3IONIZATIONOFWEAKELECTROLYTES
โ๏ธ Acids & bases have small K value
๐ Example:
CHโCOOH โ Hโบ + CHโCOOโป
โ๏ธ Small K โ weak acid
9๏ธโฃ #APPLICATION4CALCULATIONOFCONCENTRATION
โ๏ธ Find unknown equilibrium concentration
โ๏ธ Used in ICE table method
๐ Steps:
โ๏ธ Initial concentration
โ๏ธ Change
โ๏ธ Equilibrium
๐ #APPLICATION5EFFECTOFCHANGINGCONDITIONS
โ๏ธ Temperature change affects K
โ๏ธ Concentration & pressure do NOT change K
๐ Only temperature changes K value
1๏ธโฃ1๏ธโฃ #EFFECTOFTEMPERATURE
โ๏ธ Endothermic reaction:
Temperature โ โ K โ
โ๏ธ Exothermic reaction:
Temperature โ โ K โ
1๏ธโฃ2๏ธโฃ #RELATIONWITHGIBBSFREEENERGY
๐ Formula:
ฮGยฐ = โRT ln K
โ๏ธ ฮGยฐ < 0 โ K > 1 (spontaneous)
โ๏ธ ฮGยฐ > 0 โ K < 1
1๏ธโฃ3๏ธโฃ #HETEROGENEOUSEQUILIBRIUM
โ๏ธ Solids & liquids not included in K
๐ Example:
CaCOโ(s) โ CaO(s) + COโ(g)
Kp = P(COโ)
1๏ธโฃ4๏ธโฃ #REVERSINGREACTION
โ๏ธ K(reverse) = 1 / K(forward)
1๏ธโฃ5๏ธโฃ #MULTIPLYINGREACTION
โ๏ธ If reaction multiplied by n
โ๏ธ New K = Kโฟ
1๏ธโฃ6๏ธโฃ #NEETโ ๏ธ
โ๏ธ K depends only on temperature
โ๏ธ Catalyst does not change K
โ๏ธ Pure solids not included
โ๏ธ Units of K depend on reaction
1๏ธโฃ7๏ธโฃ #ONELINEREVISION
โ๏ธ K predicts extent of reaction
โ๏ธ Q vs K gives direction
โ๏ธ Only temperature affects K
โ๏ธ KpโKc relation important
โค3๐2๐2๐ฏ1
โฃ #SOLUBILITYPRODUCT
โ๏ธ Solubility product = product of molar concentrations of ions in saturated solution
โ๏ธ Each concentration raised to power of its stoichiometric coefficient
๐ For salt: AโBแตง
Ksp = [Aโบ]หฃ [Bโป]สธ
2๏ธโฃ #CONDITIONOFAPPLICABILITY
โ๏ธ Salt must be sparingly soluble
โ๏ธ Solution must be saturated
โ๏ธ At constant temperature
.
3๏ธโฃ #IONICDISSOCIATION
โ๏ธ AB(s) โ Aโบ + Bโป
โ๏ธ AโB(s) โ 2Aโบ + Bยฒโป
โ๏ธ ABโ(s) โ Aโบ + 2Bโป
.
4๏ธโฃ #MOLARSOLUBILITY (S)
โ๏ธ Molar solubility = moles dissolved per litre to form saturated solution
๐ Units: mol Lโปยน
โญโญ5๏ธโฃ #KspINTERMSSOLUBILITY (VERY IMP )
5๏ธโฃ1๏ธโฃ For AB
AB โ Aโบ + Bโป
Ksp = Sยฒ
S = โKsp
5๏ธโฃ2๏ธโฃ For AโB
AโB โ 2Aโบ + Bยฒโป
Ksp = (2S)ยฒ(S) = 4Sยณ
S = (Ksp / 4)ยนแยณ
5๏ธโฃ3๏ธโฃ For ABโ
ABโ โ Aโบ + 2Bโป
Ksp = S(2S)ยฒ = 4Sยณ
S = (Ksp / 4)ยนแยณ
5๏ธโฃ4๏ธโฃ For AโB
AโB โ 3Aโบ + Bยณโป
Ksp = (3S)ยณ(S) = 27Sโด
6๏ธโฃ #IONICPRODUCT (IP)
โ๏ธ IP = product of ionic concentrations at any instant
๐ Comparison:
โ๏ธ IP < Ksp โ Unsaturated
โ๏ธ IP = Ksp โ Saturated
โ๏ธ IP > Ksp โ Precipitation
.
7๏ธโฃ #COMMONIONEFFECT (NEET )
โ๏ธ Solubility decreases in presence of common ion
๐ Example:
AgCl solubility โ in NaCl solution
๐ Reason: Equilibrium shifts backward
8๏ธโฃ #EFFECTOFPHONCOMMONION
โ๏ธ Solubility increases if no common ion present
9๏ธโฃ #SELECTIVEPRECIPITATION
โ๏ธ Salt with lower Ksp precipitates first
๐ Used in qualitative analysis
๐ #RELATIONBETWEENSOLUBILITYANDKsp
โ๏ธ Higher Ksp โ higher solubility always
โ๏ธ Depends on stoichiometry of salt
1๏ธโฃ1๏ธโฃ #SOLUBILITYINPRESENCEOFCOMMONION
For AB in presence of Bโป concentration = C
Ksp = S ร C
S = Ksp / C
๐ Used in buffer & salt solutions
1๏ธโฃ2๏ธโฃ #SOLUBILITYINPRESENCEOFPH
โ๏ธ For salts of weak acids โ solubility increases in acidic medium
โ๏ธ For salts of weak bases โ solubility increases in basic medium
๐ Example:
CaCOโ dissolves more in acidic solution
1๏ธโฃ3๏ธโฃ #TEMPERATUREEFFECT
โ๏ธ Ksp increases with temperature (usually)
โ๏ธ Endothermic dissolution favoured
1๏ธโฃ4๏ธโฃ #UNITOFKsp
โ๏ธ Depends on stoichiometry
โ๏ธ No fixed unit
๐ NEET note: Ksp has no unit
1๏ธโฃ5๏ธโฃ #COMPARISONOFKspVALUES
โ๏ธ Compare only salts with same formula type
โ๏ธ Otherwise comparison invalid
1๏ธโฃ6๏ธโฃ #PRECIPITATIONCONDITION
โ๏ธ Precipitation starts when IP just exceeds Ksp
1๏ธโฃ7๏ธโฃ #SOLUBILITYORDER
โ๏ธ Lower Ksp โ lower solubility (for same type salts)
1๏ธโฃ8๏ธโฃ #NEETโ ๏ธTRAPS
โ๏ธ Ksp valid only for saturated solution
โ๏ธ Ksp โ solubility
โ๏ธ Common ion reduces solubility
โ๏ธ Ksp independent of initial concentration
โ๏ธ Compare Ksp only at same temperature
1๏ธโฃ9๏ธโฃ #NUMERICALSHORTCUT
โ๏ธ If Ksp = 10โปยนโฐ for AB
S โ 10โปโต
โ๏ธ If Ksp = 4ร10โปยนยฒ for ABโ
S โ 10โปโด
2๏ธโฃ0๏ธโฃ #ONELINEREVISION
โ๏ธ Ksp = ionic product at saturation
โ๏ธ Precipitation when IP > Ksp
โ๏ธ Common ion โ solubility
โ๏ธ Same Ksp โ same solubility
โ๏ธ Solubility product = product of molar concentrations of ions in saturated solution
โ๏ธ Each concentration raised to power of its stoichiometric coefficient
๐ For salt: AโBแตง
Ksp = [Aโบ]หฃ [Bโป]สธ
2๏ธโฃ #CONDITIONOFAPPLICABILITY
โ๏ธ Salt must be sparingly soluble
โ๏ธ Solution must be saturated
โ๏ธ At constant temperature
.
3๏ธโฃ #IONICDISSOCIATION
โ๏ธ AB(s) โ Aโบ + Bโป
โ๏ธ AโB(s) โ 2Aโบ + Bยฒโป
โ๏ธ ABโ(s) โ Aโบ + 2Bโป
.
4๏ธโฃ #MOLARSOLUBILITY (S)
โ๏ธ Molar solubility = moles dissolved per litre to form saturated solution
๐ Units: mol Lโปยน
โญโญ5๏ธโฃ #KspINTERMSSOLUBILITY (VERY IMP )
5๏ธโฃ1๏ธโฃ For AB
AB โ Aโบ + Bโป
Ksp = Sยฒ
S = โKsp
5๏ธโฃ2๏ธโฃ For AโB
AโB โ 2Aโบ + Bยฒโป
Ksp = (2S)ยฒ(S) = 4Sยณ
S = (Ksp / 4)ยนแยณ
5๏ธโฃ3๏ธโฃ For ABโ
ABโ โ Aโบ + 2Bโป
Ksp = S(2S)ยฒ = 4Sยณ
S = (Ksp / 4)ยนแยณ
5๏ธโฃ4๏ธโฃ For AโB
AโB โ 3Aโบ + Bยณโป
Ksp = (3S)ยณ(S) = 27Sโด
6๏ธโฃ #IONICPRODUCT (IP)
โ๏ธ IP = product of ionic concentrations at any instant
๐ Comparison:
โ๏ธ IP < Ksp โ Unsaturated
โ๏ธ IP = Ksp โ Saturated
โ๏ธ IP > Ksp โ Precipitation
.
7๏ธโฃ #COMMONIONEFFECT (NEET )
โ๏ธ Solubility decreases in presence of common ion
๐ Example:
AgCl solubility โ in NaCl solution
๐ Reason: Equilibrium shifts backward
8๏ธโฃ #EFFECTOFPHONCOMMONION
โ๏ธ Solubility increases if no common ion present
9๏ธโฃ #SELECTIVEPRECIPITATION
โ๏ธ Salt with lower Ksp precipitates first
๐ Used in qualitative analysis
๐ #RELATIONBETWEENSOLUBILITYANDKsp
โ๏ธ Higher Ksp โ higher solubility always
โ๏ธ Depends on stoichiometry of salt
1๏ธโฃ1๏ธโฃ #SOLUBILITYINPRESENCEOFCOMMONION
For AB in presence of Bโป concentration = C
Ksp = S ร C
S = Ksp / C
๐ Used in buffer & salt solutions
1๏ธโฃ2๏ธโฃ #SOLUBILITYINPRESENCEOFPH
โ๏ธ For salts of weak acids โ solubility increases in acidic medium
โ๏ธ For salts of weak bases โ solubility increases in basic medium
๐ Example:
CaCOโ dissolves more in acidic solution
1๏ธโฃ3๏ธโฃ #TEMPERATUREEFFECT
โ๏ธ Ksp increases with temperature (usually)
โ๏ธ Endothermic dissolution favoured
1๏ธโฃ4๏ธโฃ #UNITOFKsp
โ๏ธ Depends on stoichiometry
โ๏ธ No fixed unit
๐ NEET note: Ksp has no unit
1๏ธโฃ5๏ธโฃ #COMPARISONOFKspVALUES
โ๏ธ Compare only salts with same formula type
โ๏ธ Otherwise comparison invalid
1๏ธโฃ6๏ธโฃ #PRECIPITATIONCONDITION
โ๏ธ Precipitation starts when IP just exceeds Ksp
1๏ธโฃ7๏ธโฃ #SOLUBILITYORDER
โ๏ธ Lower Ksp โ lower solubility (for same type salts)
1๏ธโฃ8๏ธโฃ #NEETโ ๏ธTRAPS
โ๏ธ Ksp valid only for saturated solution
โ๏ธ Ksp โ solubility
โ๏ธ Common ion reduces solubility
โ๏ธ Ksp independent of initial concentration
โ๏ธ Compare Ksp only at same temperature
1๏ธโฃ9๏ธโฃ #NUMERICALSHORTCUT
โ๏ธ If Ksp = 10โปยนโฐ for AB
S โ 10โปโต
โ๏ธ If Ksp = 4ร10โปยนยฒ for ABโ
S โ 10โปโด
2๏ธโฃ0๏ธโฃ #ONELINEREVISION
โ๏ธ Ksp = ionic product at saturation
โ๏ธ Precipitation when IP > Ksp
โ๏ธ Common ion โ solubility
โ๏ธ Same Ksp โ same solubility
โค2๐ฏ2๐1
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โค2๐1๐1๐คฉ1
Q1
Assertion (A): Solubility of AgCl decreases on addition of NaCl.
Reason (R): Addition of NaCl increases concentration of Clโป ions.
Q2
Assertion (A): Larger the value of Ksp, higher is the solubility of a salt.
Reason (R): Ksp is directly proportional to solubility for all salts
Q3
Assertion (A): Precipitation occurs when ionic product exceeds Ksp.
Reason (R): Solution becomes supersaturated under this condition.
Q4
Assertion (A): Solubility of BaSOโ increases in presence of dilute HCl.
Reason (R): Hโบ ions react with SOโยฒโป ions to form HSOโโป.
Q5
Assertion (A): Two salts having same Ksp may have different solubilities.
Reason (R): Solubility depends on number of ions produced on dissociation
.
โค1๐1
1๏ธโฃ #WEAKELECTROLYTES
โ๏ธ Weak acids & weak bases ionise partially in aqueous solution
โ๏ธ Establish equilibrium between ionised & unionised form
๐ Examples:
โ๏ธ Weak acid โ CHโCOOH
โ๏ธ Weak base โ NHโOH
2๏ธโฃ #IONISATIONOFWEAKACID
โ๏ธ Partial dissociation in water
๐ General reaction:
HA + HโO โ HโOโบ + Aโป
๐ Example:
CHโCOOH + HโO โ HโOโบ + CHโCOOโป
3๏ธโฃ #ACIDDISSOCIATIONCONSTANT (Ka)
โ๏ธ Measure of strength of weak acid
โ๏ธ Higher Ka โ stronger acid
๐ Expression:
Ka = [Hโบ][Aโป] / [HA]
โ๏ธ Unit: mol Lโปยน
4๏ธโฃ #DEGREEOFIONISATION (ฮฑ)
โ๏ธ Fraction of total molecules ionised
๐ Formula:
ฮฑ = Number of molecules ionised / Total molecules
โ๏ธ For weak acids โ ฮฑ โช 1
5๏ธโฃ #RELATIONBETWEENKaANDฮฑ (NEET FAV )
For weak acid of concentration C:
๐ Formula:
Ka = Cฮฑยฒ
๐ Therefore:
ฮฑ = โ(Ka / C)
โ๏ธ Ionisation increases on dilution
6๏ธโฃ #pKaCONCEPT
โ๏ธ pKa = โlog Ka
โ๏ธ Lower pKa โ stronger acid
๐ Relation:
Strong acid โ small pKa
Weak acid โ large pKa
7๏ธโฃ #pHOFWEAKACID
For weak acid of concentration C:
๐ Formula:
[Hโบ] = โ(Ka ร C)
๐ pH formula:
pH = ยฝ ( pKa โ log C )
โ๏ธ Very important for numericals
8๏ธโฃ #IONISATIONOFWEAKBASE
โ๏ธ Partial dissociation in water
๐ General reaction:
BOH โ Bโบ + OHโป
๐ Example:
NHโOH โ NHโโบ + OHโป
9๏ธโฃ #BASEDISSOCIATIONCONSTANT (Kb)
โ๏ธ Measure of strength of weak base
โ๏ธ Higher Kb โ stronger base
๐ Expression:
Kb = [Bโบ][OHโป] / [BOH]
๐ #RELATIONBETWEENKbANDฮฑ
For weak base of concentration C:
๐ Formula:
Kb = Cฮฑยฒ
๐ Therefore:
ฮฑ = โ(Kb / C)
1๏ธโฃ1๏ธโฃ #pKbCONCEPT
โ๏ธ pKb = โlog Kb
โ๏ธ Lower pKb โ stronger base
1๏ธโฃ2๏ธโฃ #pHOFWEAKBASE
For weak base of concentration C:
๐ [OHโป] = โ(Kb ร C)
๐ pOH formula:
pOH = ยฝ ( pKb โ log C )
๐ pH = 14 โ pOH
1๏ธโฃ3๏ธโฃ #DILUTIONEFFECT (VERY IMP ๐ฅ)
โ๏ธ On dilution โ degree of ionisation increases
โ๏ธ But total ions per unit volume decrease
๐ Ostwaldโs dilution law applies
1๏ธโฃ4๏ธโฃ #COMMONIONEFFECT
โ๏ธ Ionisation of weak electrolyte decreases
โ๏ธ Presence of common ion shifts equilibrium backward
๐ Example:
CHโCOOH + CHโCOONa โ ionisation decreases
1๏ธโฃ5๏ธโฃ #WEAKACIDVSWEAKBASE
โ๏ธ Weak acid โ Hโบ producing
โ๏ธ Weak base โ OHโป producing
โ๏ธ Both show partial ionisation
1๏ธโฃ6๏ธโฃ #NEETโ ๏ธKEYPOINTS
โ๏ธ Ka & Kb are temperature dependent
โ๏ธ ฮฑ increases with dilution
โ๏ธ pH of weak acid > strong acid (same concentration)
โ๏ธ pH of weak base < strong base (same concentration)
1๏ธโฃ7๏ธโฃ #ONELINEREVISION
โ๏ธ Weak electrolytes ionise partially
โ๏ธ Ka = Cฮฑยฒ
โ๏ธ [Hโบ] = โ(Ka ร C)
โ๏ธ pH weak acid = ยฝ (pKa โ log C)
โ๏ธ Dilution increases ionisation
โ๏ธ Weak acids & weak bases ionise partially in aqueous solution
โ๏ธ Establish equilibrium between ionised & unionised form
๐ Examples:
โ๏ธ Weak acid โ CHโCOOH
โ๏ธ Weak base โ NHโOH
2๏ธโฃ #IONISATIONOFWEAKACID
โ๏ธ Partial dissociation in water
๐ General reaction:
HA + HโO โ HโOโบ + Aโป
๐ Example:
CHโCOOH + HโO โ HโOโบ + CHโCOOโป
3๏ธโฃ #ACIDDISSOCIATIONCONSTANT (Ka)
โ๏ธ Measure of strength of weak acid
โ๏ธ Higher Ka โ stronger acid
๐ Expression:
Ka = [Hโบ][Aโป] / [HA]
โ๏ธ Unit: mol Lโปยน
4๏ธโฃ #DEGREEOFIONISATION (ฮฑ)
โ๏ธ Fraction of total molecules ionised
๐ Formula:
ฮฑ = Number of molecules ionised / Total molecules
โ๏ธ For weak acids โ ฮฑ โช 1
5๏ธโฃ #RELATIONBETWEENKaANDฮฑ (NEET FAV )
For weak acid of concentration C:
๐ Formula:
Ka = Cฮฑยฒ
๐ Therefore:
ฮฑ = โ(Ka / C)
โ๏ธ Ionisation increases on dilution
6๏ธโฃ #pKaCONCEPT
โ๏ธ pKa = โlog Ka
โ๏ธ Lower pKa โ stronger acid
๐ Relation:
Strong acid โ small pKa
Weak acid โ large pKa
7๏ธโฃ #pHOFWEAKACID
For weak acid of concentration C:
๐ Formula:
[Hโบ] = โ(Ka ร C)
๐ pH formula:
pH = ยฝ ( pKa โ log C )
โ๏ธ Very important for numericals
8๏ธโฃ #IONISATIONOFWEAKBASE
โ๏ธ Partial dissociation in water
๐ General reaction:
BOH โ Bโบ + OHโป
๐ Example:
NHโOH โ NHโโบ + OHโป
9๏ธโฃ #BASEDISSOCIATIONCONSTANT (Kb)
โ๏ธ Measure of strength of weak base
โ๏ธ Higher Kb โ stronger base
๐ Expression:
Kb = [Bโบ][OHโป] / [BOH]
๐ #RELATIONBETWEENKbANDฮฑ
For weak base of concentration C:
๐ Formula:
Kb = Cฮฑยฒ
๐ Therefore:
ฮฑ = โ(Kb / C)
1๏ธโฃ1๏ธโฃ #pKbCONCEPT
โ๏ธ pKb = โlog Kb
โ๏ธ Lower pKb โ stronger base
1๏ธโฃ2๏ธโฃ #pHOFWEAKBASE
For weak base of concentration C:
๐ [OHโป] = โ(Kb ร C)
๐ pOH formula:
pOH = ยฝ ( pKb โ log C )
๐ pH = 14 โ pOH
1๏ธโฃ3๏ธโฃ #DILUTIONEFFECT (VERY IMP ๐ฅ)
โ๏ธ On dilution โ degree of ionisation increases
โ๏ธ But total ions per unit volume decrease
๐ Ostwaldโs dilution law applies
1๏ธโฃ4๏ธโฃ #COMMONIONEFFECT
โ๏ธ Ionisation of weak electrolyte decreases
โ๏ธ Presence of common ion shifts equilibrium backward
๐ Example:
CHโCOOH + CHโCOONa โ ionisation decreases
1๏ธโฃ5๏ธโฃ #WEAKACIDVSWEAKBASE
โ๏ธ Weak acid โ Hโบ producing
โ๏ธ Weak base โ OHโป producing
โ๏ธ Both show partial ionisation
1๏ธโฃ6๏ธโฃ #NEETโ ๏ธKEYPOINTS
โ๏ธ Ka & Kb are temperature dependent
โ๏ธ ฮฑ increases with dilution
โ๏ธ pH of weak acid > strong acid (same concentration)
โ๏ธ pH of weak base < strong base (same concentration)
1๏ธโฃ7๏ธโฃ #ONELINEREVISION
โ๏ธ Weak electrolytes ionise partially
โ๏ธ Ka = Cฮฑยฒ
โ๏ธ [Hโบ] = โ(Ka ร C)
โ๏ธ pH weak acid = ยฝ (pKa โ log C)
โ๏ธ Dilution increases ionisation
โค5๐ฏ2๐ฅ1
1๏ธโฃ #REDOXREACTION
โ๏ธ Redox reaction = reaction involving simultaneous oxidation and reduction
โ๏ธ Oxidation โ loss of electrons
โ๏ธ Reduction โ gain of electrons
๐ Example:
Zn + Cuยฒโบ โ Znยฒโบ + Cu
โ๏ธ Zn โ Znยฒโบ + 2eโป (Oxidation)
โ๏ธ Cuยฒโบ + 2eโป โ Cu (Reduction)
2๏ธโฃ #OXIDATIONNUMBERCONCEPT
โ๏ธ Oxidation number (ON) = hypothetical charge if all bonds ionic
โ๏ธ Increase in ON โ oxidation
โ๏ธ Decrease in ON โ reduction
๐ Rules:
โ๏ธ Element in free state โ ON = 0
โ๏ธ Monatomic ion โ ON = charge
โ๏ธ Oxygen โ usually โ2
โ๏ธ Hydrogen โ usually +1
โ๏ธ Sum of ONs in molecule โ 0
โ๏ธ Sum of ONs in polyatomic ion โ ion charge
3๏ธโฃ #TYPESOFREDOXREACTIONS
โ๏ธ Combination reaction โ A + B โ AB
โ๏ธ Decomposition โ AB โ A + B
โ๏ธ Displacement โ A + BC โ AC + B
โ๏ธ Disproportionation โ X โ Xโฟโบ + Xแตโป
๐ Example:
2HโOโ โ 2HโO + Oโ
โ๏ธ O in HโOโ: โ1 โ 0 & โ2 (disproportionation)
4๏ธโฃ #OXIDISINGAGENT
โ๏ธ Substance that accepts electrons
โ๏ธ Causes oxidation of other species
๐ Example:
โ๏ธ Cuยฒโบ in Zn + Cuยฒโบ โ Cuยฒโบ is oxidising agent
5๏ธโฃ #REDUCINGAGENT
โ๏ธ Substance that donates electrons
โ๏ธ Causes reduction of other species
๐ Example:
โ๏ธ Zn in Zn + Cuยฒโบ โ Zn is reducing agent
6๏ธโฃ #ELECTRONBALANCEMETHOD (NEET FAV )
โ๏ธ Step 1 โ Write oxidation & reduction half-reactions
โ๏ธ Step 2 โ Balance atoms other than O & H
โ๏ธ Step 3 โ Balance O by HโO
โ๏ธ Step 4 โ Balance H by Hโบ (acidic) or OHโป (basic)
โ๏ธ Step 5 โ Balance electrons
โ๏ธ Step 6 โ Combine half-reactions
7๏ธโฃ #IONICEQUATIONEXAMPLE
โ๏ธ Feยฒโบ + CrโOโยฒโป โ Feยณโบ + Crยณโบ (acidic medium)
๐ Half-reactions:
Feยฒโบ โ Feยณโบ + eโป
CrโOโยฒโป + 14Hโบ + 6eโป โ 2Crยณโบ + 7HโO
๐ Multiply Fe reaction by 6 โ 6Feยฒโบ โ 6Feยณโบ + 6eโป
๐ Combine โ 6Feยฒโบ + CrโOโยฒโป + 14Hโบ โ 6Feยณโบ + 2Crยณโบ + 7HโO
8๏ธโฃ #DISPROPORTIONATIONREACTIONS
โ๏ธ Same element undergoes oxidation & reduction simultaneously
๐ Example:
3Clโ + 6OHโป โ 5Clโป + ClOโโป + 3HโO
โ๏ธ Cl โ โ1 & +5
9๏ธโฃ #NEETโ ๏ธKEYPOINTS
โ๏ธ Redox can occur in acidic or basic medium
โ๏ธ Use oxidation number method for quick identification
โ๏ธ Disproportionation = special redox with same element
โ๏ธ Oxidising & reducing agents always appear on opposite sides
1๏ธโฃ0๏ธโฃ #ONELINEREVISION
โ๏ธ Redox = Oxidation + Reduction
โ๏ธ Oxidation โ loss eโป, ON โ
โ๏ธ Reduction โ gain eโป, ON โ
โ๏ธ Oxidising agent โ gains eโป
โ๏ธ Reducing agent โ loses eโป
โ๏ธ Use half-reaction method for balancing
โ๏ธ Redox reaction = reaction involving simultaneous oxidation and reduction
โ๏ธ Oxidation โ loss of electrons
โ๏ธ Reduction โ gain of electrons
๐ Example:
Zn + Cuยฒโบ โ Znยฒโบ + Cu
โ๏ธ Zn โ Znยฒโบ + 2eโป (Oxidation)
โ๏ธ Cuยฒโบ + 2eโป โ Cu (Reduction)
2๏ธโฃ #OXIDATIONNUMBERCONCEPT
โ๏ธ Oxidation number (ON) = hypothetical charge if all bonds ionic
โ๏ธ Increase in ON โ oxidation
โ๏ธ Decrease in ON โ reduction
๐ Rules:
โ๏ธ Element in free state โ ON = 0
โ๏ธ Monatomic ion โ ON = charge
โ๏ธ Oxygen โ usually โ2
โ๏ธ Hydrogen โ usually +1
โ๏ธ Sum of ONs in molecule โ 0
โ๏ธ Sum of ONs in polyatomic ion โ ion charge
3๏ธโฃ #TYPESOFREDOXREACTIONS
โ๏ธ Combination reaction โ A + B โ AB
โ๏ธ Decomposition โ AB โ A + B
โ๏ธ Displacement โ A + BC โ AC + B
โ๏ธ Disproportionation โ X โ Xโฟโบ + Xแตโป
๐ Example:
2HโOโ โ 2HโO + Oโ
โ๏ธ O in HโOโ: โ1 โ 0 & โ2 (disproportionation)
4๏ธโฃ #OXIDISINGAGENT
โ๏ธ Substance that accepts electrons
โ๏ธ Causes oxidation of other species
๐ Example:
โ๏ธ Cuยฒโบ in Zn + Cuยฒโบ โ Cuยฒโบ is oxidising agent
5๏ธโฃ #REDUCINGAGENT
โ๏ธ Substance that donates electrons
โ๏ธ Causes reduction of other species
๐ Example:
โ๏ธ Zn in Zn + Cuยฒโบ โ Zn is reducing agent
6๏ธโฃ #ELECTRONBALANCEMETHOD (NEET FAV )
โ๏ธ Step 1 โ Write oxidation & reduction half-reactions
โ๏ธ Step 2 โ Balance atoms other than O & H
โ๏ธ Step 3 โ Balance O by HโO
โ๏ธ Step 4 โ Balance H by Hโบ (acidic) or OHโป (basic)
โ๏ธ Step 5 โ Balance electrons
โ๏ธ Step 6 โ Combine half-reactions
7๏ธโฃ #IONICEQUATIONEXAMPLE
โ๏ธ Feยฒโบ + CrโOโยฒโป โ Feยณโบ + Crยณโบ (acidic medium)
๐ Half-reactions:
Feยฒโบ โ Feยณโบ + eโป
CrโOโยฒโป + 14Hโบ + 6eโป โ 2Crยณโบ + 7HโO
๐ Multiply Fe reaction by 6 โ 6Feยฒโบ โ 6Feยณโบ + 6eโป
๐ Combine โ 6Feยฒโบ + CrโOโยฒโป + 14Hโบ โ 6Feยณโบ + 2Crยณโบ + 7HโO
8๏ธโฃ #DISPROPORTIONATIONREACTIONS
โ๏ธ Same element undergoes oxidation & reduction simultaneously
๐ Example:
3Clโ + 6OHโป โ 5Clโป + ClOโโป + 3HโO
โ๏ธ Cl โ โ1 & +5
9๏ธโฃ #NEETโ ๏ธKEYPOINTS
โ๏ธ Redox can occur in acidic or basic medium
โ๏ธ Use oxidation number method for quick identification
โ๏ธ Disproportionation = special redox with same element
โ๏ธ Oxidising & reducing agents always appear on opposite sides
1๏ธโฃ0๏ธโฃ #ONELINEREVISION
โ๏ธ Redox = Oxidation + Reduction
โ๏ธ Oxidation โ loss eโป, ON โ
โ๏ธ Reduction โ gain eโป, ON โ
โ๏ธ Oxidising agent โ gains eโป
โ๏ธ Reducing agent โ loses eโป
โ๏ธ Use half-reaction method for balancing
โค3๐ฅ3๐1๐1
โค2๐ณ1
๐2๐1
Periodic table order
Exceptional like
1st โญ#Radii grp 13 p block al>Ga
d series mn 3d5 sw so vahi sw reverse then fe=co=ni then cu<zn
2nd โญ #IE 3d<4d<5d but in 4th to 12th grp
4d=5d (appro) LC.
In grp 13 Beet, GAI
14th pb>sn
3rd โญEA : 2nd period se 3rd vale ki hmesha jyada
Highest Cl
Oxygen family M O last m
Exceptional like
1st โญ#Radii grp 13 p block al>Ga
d series mn 3d5 sw so vahi sw reverse then fe=co=ni then cu<zn
2nd โญ #IE 3d<4d<5d but in 4th to 12th grp
4d=5d (appro) LC.
In grp 13 Beet, GAI
14th pb>sn
3rd โญEA : 2nd period se 3rd vale ki hmesha jyada
Highest Cl
Oxygen family M O last m
โค2๐ฅ2๐2๐ฏ1
1๏ธโฃ #CARBONFAMILY
โ๏ธ Group number โ 14
โ๏ธ General electronic configuration:
๐ nsยฒ npยฒ
โ๏ธ Members:
โ๏ธ Carbon (C)
โ๏ธ Silicon (Si)
โ๏ธ Germanium (Ge)
โ๏ธ Tin (Sn)
โ๏ธ Lead (Pb)
2๏ธโฃ #POSITIONINPERIODICTABLE
โ๏ธ Lies between Boron family (13) & Nitrogen family (15)
โ๏ธ First group containing non-metal โ metalloid โ metal trend
๐ Nature trend:
โ๏ธ C โ Non-metal
โ๏ธ Si, Ge โ Metalloids
โ๏ธ Sn, Pb โ Metals
3๏ธโฃ #ATOMICANDPHYSICALPROPERTIES
โ๏ธ Atomic radius โ down the group
โ๏ธ Ionisation enthalpy โ down the group
โ๏ธ Electronegativity โ down the group
๐ Density:
โ๏ธ Increases downwards (exception: Pb irregularity)
4๏ธโฃ #COVALENTCHARACTER
โ๏ธ Strong covalent bonding (especially C, Si)
โ๏ธ Due to:
โ๏ธ Small size
โ๏ธ High electronegativity
๐ Carbon shows maximum covalency (4)
5๏ธโฃ #OXIDATIONSTATES โญ VERY IMP
โ๏ธ Common oxidation states:
โ๏ธ +4 and +2
๐ Stability trend:
โ๏ธ +4 stable for C, Si
โ๏ธ +2 stability โ down the group
๐ Reason:
โ๏ธ Inert pair effect (Sn, Pb)
๐ Examples:
โ๏ธ COโ โ +4
โ๏ธ CO โ +2
โ๏ธ SnClโ (+2) more stable than SnClโ
6๏ธโฃ #INERTPAIREFFECT
โ๏ธ Poor shielding of d & f electrons
โ๏ธ nsยฒ electrons less available for bonding
๐ Order:
C < Si < Ge < Sn < Pb
โ๏ธ Pb shows strongest inert pair effect
7๏ธโฃ #CATABENATION (NEET FAV )
โ๏ธ Ability to form long chains
๐ Order:
C >>> Si > Ge > Sn > Pb
๐ Reason:
โ๏ธ Strong CโC bond
โ๏ธ Small atomic size
โ๏ธ Carbon forms:
โ๏ธ Straight chains
โ๏ธ Branched chains
โ๏ธ Rings
8๏ธโฃ #ALLOTROPY
โ๏ธ Carbon shows extensive allotropy
๐ Allotropes of carbon:
โ๏ธ Diamond โ hardest, spยณ
โ๏ธ Graphite โ conductor, spยฒ
โ๏ธ Fullerene (Cโโ)
โ๏ธ Si, Ge show limited allotropy
9๏ธโฃ #HYDRIDES
โ๏ธ General formula: MHโ
๐ Examples:
โ๏ธ CHโ โ Methane
โ๏ธ SiHโ โ Silane
๐ Stability:
CHโ > SiHโ > GeHโ > SnHโ
โ๏ธ Reducing character โ down group
1๏ธโฃ0๏ธโฃ #HALIDES
โ๏ธ General formula: MXโ
๐ Examples:
โ๏ธ CClโ
โ๏ธ SiClโ
๐ Hydrolysis:
โ๏ธ CClโ โ no hydrolysis
โ๏ธ SiClโ โ hydrolyses easily
๐ Reason:
โ๏ธ Availability of vacant d-orbitals in Si
1๏ธโฃ1๏ธโฃ #OXIDES
โ๏ธ General formula: MOโ
๐ Nature:
โ๏ธ COโ โ acidic
โ๏ธ SiOโ โ weakly acidic
โ๏ธ SnOโ, PbOโ โ amphoteric
๐ Acidity โ down the group
1๏ธโฃ2๏ธโฃ #ANOMALOUSBEHAVIOUROFCARBON
โ๏ธ Small size
โ๏ธ High electronegativity
โ๏ธ Strong pฯโpฯ bonding
โ๏ธ Maximum catenation
โ๏ธ No d-orbitals
๐ Hence carbon differs from rest of group
1๏ธโฃ3๏ธโฃ #USES (NEET RELEVANT)
โ๏ธ Carbon โ fuels, organic compounds
โ๏ธ Silicon โ semiconductors, glass
โ๏ธ Tin โ coating (tin cans)
โ๏ธ Lead โ batteries, radiation shielding
1๏ธโฃ4๏ธโฃ #NEETKEYPOINTS
โ๏ธ +2 oxidation state stability โ down group
โ๏ธ Inert pair effect strongest in Pb
โ๏ธ Carbon shows maximum catenation
โ๏ธ COโ acidic, PbOโ amphoteric
1๏ธโฃ5๏ธโฃ #ONELINEREVISION
โ๏ธ Group 14 โ nsยฒ npยฒ
โ๏ธ C non-metal โ Pb metal
โ๏ธ Oxidation states +4, +2
โ๏ธ Inert pair effect important
โ๏ธ Carbon is exceptional
โ๏ธ Group number โ 14
โ๏ธ General electronic configuration:
๐ nsยฒ npยฒ
โ๏ธ Members:
โ๏ธ Carbon (C)
โ๏ธ Silicon (Si)
โ๏ธ Germanium (Ge)
โ๏ธ Tin (Sn)
โ๏ธ Lead (Pb)
2๏ธโฃ #POSITIONINPERIODICTABLE
โ๏ธ Lies between Boron family (13) & Nitrogen family (15)
โ๏ธ First group containing non-metal โ metalloid โ metal trend
๐ Nature trend:
โ๏ธ C โ Non-metal
โ๏ธ Si, Ge โ Metalloids
โ๏ธ Sn, Pb โ Metals
3๏ธโฃ #ATOMICANDPHYSICALPROPERTIES
โ๏ธ Atomic radius โ down the group
โ๏ธ Ionisation enthalpy โ down the group
โ๏ธ Electronegativity โ down the group
๐ Density:
โ๏ธ Increases downwards (exception: Pb irregularity)
4๏ธโฃ #COVALENTCHARACTER
โ๏ธ Strong covalent bonding (especially C, Si)
โ๏ธ Due to:
โ๏ธ Small size
โ๏ธ High electronegativity
๐ Carbon shows maximum covalency (4)
5๏ธโฃ #OXIDATIONSTATES โญ VERY IMP
โ๏ธ Common oxidation states:
โ๏ธ +4 and +2
๐ Stability trend:
โ๏ธ +4 stable for C, Si
โ๏ธ +2 stability โ down the group
๐ Reason:
โ๏ธ Inert pair effect (Sn, Pb)
๐ Examples:
โ๏ธ COโ โ +4
โ๏ธ CO โ +2
โ๏ธ SnClโ (+2) more stable than SnClโ
6๏ธโฃ #INERTPAIREFFECT
โ๏ธ Poor shielding of d & f electrons
โ๏ธ nsยฒ electrons less available for bonding
๐ Order:
C < Si < Ge < Sn < Pb
โ๏ธ Pb shows strongest inert pair effect
7๏ธโฃ #CATABENATION (NEET FAV )
โ๏ธ Ability to form long chains
๐ Order:
C >>> Si > Ge > Sn > Pb
๐ Reason:
โ๏ธ Strong CโC bond
โ๏ธ Small atomic size
โ๏ธ Carbon forms:
โ๏ธ Straight chains
โ๏ธ Branched chains
โ๏ธ Rings
8๏ธโฃ #ALLOTROPY
โ๏ธ Carbon shows extensive allotropy
๐ Allotropes of carbon:
โ๏ธ Diamond โ hardest, spยณ
โ๏ธ Graphite โ conductor, spยฒ
โ๏ธ Fullerene (Cโโ)
โ๏ธ Si, Ge show limited allotropy
9๏ธโฃ #HYDRIDES
โ๏ธ General formula: MHโ
๐ Examples:
โ๏ธ CHโ โ Methane
โ๏ธ SiHโ โ Silane
๐ Stability:
CHโ > SiHโ > GeHโ > SnHโ
โ๏ธ Reducing character โ down group
1๏ธโฃ0๏ธโฃ #HALIDES
โ๏ธ General formula: MXโ
๐ Examples:
โ๏ธ CClโ
โ๏ธ SiClโ
๐ Hydrolysis:
โ๏ธ CClโ โ no hydrolysis
โ๏ธ SiClโ โ hydrolyses easily
๐ Reason:
โ๏ธ Availability of vacant d-orbitals in Si
1๏ธโฃ1๏ธโฃ #OXIDES
โ๏ธ General formula: MOโ
๐ Nature:
โ๏ธ COโ โ acidic
โ๏ธ SiOโ โ weakly acidic
โ๏ธ SnOโ, PbOโ โ amphoteric
๐ Acidity โ down the group
1๏ธโฃ2๏ธโฃ #ANOMALOUSBEHAVIOUROFCARBON
โ๏ธ Small size
โ๏ธ High electronegativity
โ๏ธ Strong pฯโpฯ bonding
โ๏ธ Maximum catenation
โ๏ธ No d-orbitals
๐ Hence carbon differs from rest of group
1๏ธโฃ3๏ธโฃ #USES (NEET RELEVANT)
โ๏ธ Carbon โ fuels, organic compounds
โ๏ธ Silicon โ semiconductors, glass
โ๏ธ Tin โ coating (tin cans)
โ๏ธ Lead โ batteries, radiation shielding
1๏ธโฃ4๏ธโฃ #NEETKEYPOINTS
โ๏ธ +2 oxidation state stability โ down group
โ๏ธ Inert pair effect strongest in Pb
โ๏ธ Carbon shows maximum catenation
โ๏ธ COโ acidic, PbOโ amphoteric
1๏ธโฃ5๏ธโฃ #ONELINEREVISION
โ๏ธ Group 14 โ nsยฒ npยฒ
โ๏ธ C non-metal โ Pb metal
โ๏ธ Oxidation states +4, +2
โ๏ธ Inert pair effect important
โ๏ธ Carbon is exceptional
โค5๐คฉ2๐1๐1