Chemistry booster series
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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
๐Ÿคฉ3โค1๐Ÿณ1
โญ ๐—–๐—œ๐—˜ ๐—ชEE (๐——๐—ก, ๐——๐—, ๐— ๐— ๐—ฆ๐—ง๐—”๐—ฅ, ๐— ๐—ž๐—š & so on) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ

โญ ๐—ข๐—Ÿ๐—— ๐—Ÿ๐—˜๐—–๐—ง๐—จ๐—ฅ๐—˜๐—ฆ โ€” ๐—จ๐—ก๐——๐— ๐—ฌ + ๐—Ÿ๐—ก ๐—ž@๐—ง๐—” + ๐—ฆ@๐—ฉ@๐—  + ๐—ข๐—ง๐—›๐—˜๐—ฅ ๐—ง๐—ข๐—ฃ ๐—ง๐—˜๐—”๐—–๐—›๐—˜๐—ฅ๐—ฆ

โญ ๐—จ๐—ก๐——๐— ๐—ฌ (๐—ง๐—ก๐— , ๐—ฅ๐——, ๐—ฌ๐—ฆ๐—ฌ, ๐—”๐—–๐—œ๐——, ๐—ฆ๐—ง ๐—ฆ๐—œ๐—ฅ, ๐—œ๐—ก๐—ฆ๐—”๐—™ ๐—”๐—Ÿ๐—œ ๐—ฆ๐—œ๐—ฅ & So On ) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ

โญ ๐—ฆ@๐—ฉ@๐—  (๐—”๐—š ๐—ฆ๐—œ๐—ฅ, ๐—”๐—ฆ๐—›๐—œ๐—ฆ๐—› ๐—•๐—”๐—๐—ฃ๐—˜๐—ฌ๐—œ ๐—ฆ๐—œ๐—ฅ, ๐—ฃ๐—”๐—ฅ๐—ฉ๐—˜๐—ญ ๐—ž๐—›๐—”๐—ก, ๐—ฉ๐—ž
๐—ฆ๐—œ๐—ฅ & ๐—ฆ๐—ข ๐—ข๐—ก) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ


โญ ๐—–๐—ข๐—ฃ๐—ฌ๐—ฅ๐—œ๐—š๐—›๐—ง ๐—•๐—”๐—–๐—ž๐—จ๐—ฃ ๐—ข๐—™ ๐—”๐—Ÿ๐—Ÿ ๐—ข๐—™ ๐—ง๐—›๐—œ๐—ฆ
๐Ÿ˜2๐Ÿ•Š1
Chemistry booster series
โญ ๐—–๐—œ๐—˜ ๐—ชEE (๐——๐—ก, ๐——๐—, ๐— ๐— ๐—ฆ๐—ง๐—”๐—ฅ, ๐— ๐—ž๐—š & so on) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ โญ ๐—ข๐—Ÿ๐—— ๐—Ÿ๐—˜๐—–๐—ง๐—จ๐—ฅ๐—˜๐—ฆ โ€” ๐—จ๐—ก๐——๐— ๐—ฌ + ๐—Ÿ๐—ก ๐—ž@๐—ง๐—” + ๐—ฆ@๐—ฉ@๐—  + ๐—ข๐—ง๐—›๐—˜๐—ฅ ๐—ง๐—ข๐—ฃ ๐—ง๐—˜๐—”๐—–๐—›๐—˜๐—ฅ๐—ฆ โญ ๐—จ๐—ก๐——๐— ๐—ฌ (๐—ง๐—ก๐— , ๐—ฅ๐——, ๐—ฌ๐—ฆ๐—ฌ, ๐—”๐—–๐—œ๐——, ๐—ฆ๐—ง ๐—ฆ๐—œ๐—ฅ, ๐—œ๐—ก๐—ฆ๐—”๐—™ ๐—”๐—Ÿ๐—œ ๐—ฆ๐—œ๐—ฅ & So On ) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ โญ ๐—ฆ@๐—ฉ@๐—  (๐—”๐—š ๐—ฆ๐—œ๐—ฅ, ๐—”๐—ฆ๐—›๐—œ๐—ฆ๐—› ๐—•๐—”๐—๐—ฃ๐—˜๐—ฌ๐—œ ๐—ฆ๐—œ๐—ฅ, ๐—ฃ๐—”๐—ฅ๐—ฉ๐—˜๐—ญ ๐—ž๐—›๐—”๐—ก, ๐—ฉ๐—ž ๐—ฆ๐—œ๐—ฅ & ๐—ฆ๐—ข ๐—ข๐—ก) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ โญ ๐—–๐—ข๐—ฃ๐—ฌ๐—ฅ๐—œ๐—š๐—›๐—งโ€ฆ
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๐ŸŽ‰1๐Ÿ•Š1๐Ÿณ1
1๏ธโƒฃ #GIBBSFREEENERGY
โœ”๏ธ Thermodynamic state function
โœ”๏ธ Determines spontaneity of process
โœ”๏ธ Denoted by G
๐Ÿ“Œ Relation:
G = H โˆ’ TS


2๏ธโƒฃ #TERMSINFORMULA
โœ”๏ธ H โ†’ Enthalpy
โœ”๏ธ T โ†’ Absolute temperature (K)
โœ”๏ธ S โ†’ Entropy
๐Ÿ“Œ Unit of G โ†’ Joule


3๏ธโƒฃ #CHANGEINGIBBSENERGY
๐Ÿ“Œ Formula:
ฮ”G = ฮ”H โˆ’ Tฮ”S
โœ”๏ธ Applies at constant T & P


4๏ธโƒฃ #SIGNIFICANCEOFฮ”G (VERY IMP )
โœ”๏ธ ฮ”G < 0 โ†’ Spontaneous process
โœ”๏ธ ฮ”G = 0 โ†’ Equilibrium
โœ”๏ธ ฮ”G > 0 โ†’ Non-spontaneous


5๏ธโƒฃ #CASESBASEDONฮ”HANDฮ”S
โœ”๏ธ ฮ”H < 0 and ฮ”S > 0
Process spontaneous at all temperatures
โœ”๏ธ ฮ”H > 0 and ฮ”S < 0
Process non-spontaneous at all temperatures
โœ”๏ธ ฮ”H < 0 and ฮ”S < 0
Spontaneous at low temperature
โœ”๏ธ ฮ”H > 0 and ฮ”S > 0
Spontaneous at high temperature


6๏ธโƒฃ #TEMPERATUREEFFECT
โœ”๏ธ Increase in T increases importance of entropy term
โœ”๏ธ Tฮ”S dominates at high temperature


7๏ธโƒฃ #GIBBSENERGYATEQUILIBRIUM
โœ”๏ธ At equilibrium:
ฮ”G = 0
๐Ÿ“Œ Relation with equilibrium constant:
ฮ”Gยฐ = โˆ’RT ln K


8๏ธโƒฃ #STANDARDGIBBSFREEENERGY
โœ”๏ธ Measured at:
โœ”๏ธ 1 bar pressure
โœ”๏ธ 298 K temperature
๐Ÿ“Œ Formula:
ฮ”Gยฐ = ฮ”Hยฐ โˆ’ Tฮ”Sยฐ


9๏ธโƒฃ #REACTIONQUOTIENTRELATION
๐Ÿ“Œ Formula:
ฮ”G = ฮ”Gยฐ + RT ln Q
โœ”๏ธ Q = reaction quotient
๐Ÿ“Œ At equilibrium Q = K


๐Ÿ”Ÿ #MAXIMUMWORKCONCEPT
โœ”๏ธ ฮ”G gives maximum non-expansion work
โœ”๏ธ Useful in electrochemistry
๐Ÿ“Œ Electrical work = โˆ’ฮ”G


1๏ธโƒฃ1๏ธโƒฃ #GIBBSENERGYINELECTROCHEMISTRY
๐Ÿ“Œ Relation:
ฮ”Gยฐ = โˆ’nFEยฐ
โœ”๏ธ n = number of electrons
โœ”๏ธ F = Faraday constant
โœ”๏ธ Eยฐ = standard emf


1๏ธโƒฃ2๏ธโƒฃ #UNITSOFฮ”G
โœ”๏ธ Joule
โœ”๏ธ kJ molโปยน (mostly used in chemistry)


1๏ธโƒฃ3๏ธโƒฃ #NEET
โœ”๏ธ ฮ”G decides feasibility, not rate
โœ”๏ธ Spontaneous โ‰  fast
โœ”๏ธ ฮ”G depends on T, P & composition
โœ”๏ธ ฮ”G is state function


1๏ธโƒฃ4๏ธโƒฃ #ONELINEREVISION
โœ”๏ธ Gibbs free energy predicts spontaneity
โœ”๏ธ ฮ”G = 0 at equilibrium
โœ”๏ธ Negative ฮ”G โ†’ feasible process
โœ”๏ธ ฮ”Gยฐ related to K and Eยฐ
๐Ÿ”ฅ2๐Ÿ‘1๐Ÿ˜1
โญ ๐—–๐—œ๐—˜ ๐—ชEE ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ (๐——๐—ก, ๐——๐—, ๐— ๐— ๐—ฆ๐—ง๐—”๐—ฅ, ๐— ๐—ž๐—š & so on) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ

โญ ๐—ข๐—Ÿ๐—— ๐—Ÿ๐—˜๐—–๐—ง๐—จ๐—ฅ๐—˜๐—ฆ ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜โ€” ๐—จ๐—ก๐——๐— ๐—ฌ + ๐—Ÿ๐—ก ๐—ž@๐—ง๐—” + ๐—ฆ@๐—ฉ@๐—  + ๐—ข๐—ง๐—›๐—˜๐—ฅ ๐—ง๐—ข๐—ฃ ๐—ง๐—˜๐—”๐—–๐—›๐—˜๐—ฅ๐—ฆ

โญ ๐—จ๐—ก๐——๐— ๐—ฌ ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ (๐—ง๐—ก๐— , ๐—ฅ๐——, ๐—ฌ๐—ฆ๐—ฌ, ๐—”๐—–๐—œ๐——, ๐—ฆ๐—ง ๐—ฆ๐—œ๐—ฅ, ๐—œ๐—ก๐—ฆ๐—”๐—™ ๐—”๐—Ÿ๐—œ ๐—ฆ๐—œ๐—ฅ & So On ) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ

โญ ๐—ฆ@๐—ฉ@๐—  ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜(๐—”๐—š ๐—ฆ๐—œ๐—ฅ, ๐—”๐—ฆ๐—›๐—œ๐—ฆ๐—› ๐—•๐—”๐—๐—ฃ๐—˜๐—ฌ๐—œ ๐—ฆ๐—œ๐—ฅ, ๐—ฃ๐—”๐—ฅ๐—ฉ๐—˜๐—ญ ๐—ž๐—›๐—”๐—ก, ๐—ฉ๐—ž
๐—ฆ๐—œ๐—ฅ & ๐—ฆ๐—ข ๐—ข๐—ก) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ


โญ ๐—–๐—ข๐—ฃ๐—ฌ๐—ฅ๐—œ๐—š๐—›๐—ง ๐—•๐—”๐—–๐—ž๐—จ๐—ฃ ๐—ข๐—™ ๐—”๐—Ÿ๐—Ÿ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ ๐—ข๐—™ ๐—ง๐—›๐—œ๐—ฆ
โค1๐Ÿ”ฅ1๐Ÿ‘1
Chemistry booster series
โญ ๐—–๐—œ๐—˜ ๐—ชEE ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ (๐——๐—ก, ๐——๐—, ๐— ๐— ๐—ฆ๐—ง๐—”๐—ฅ, ๐— ๐—ž๐—š & so on) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ โญ ๐—ข๐—Ÿ๐—— ๐—Ÿ๐—˜๐—–๐—ง๐—จ๐—ฅ๐—˜๐—ฆ ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜โ€” ๐—จ๐—ก๐——๐— ๐—ฌ + ๐—Ÿ๐—ก ๐—ž@๐—ง๐—” + ๐—ฆ@๐—ฉ@๐—  + ๐—ข๐—ง๐—›๐—˜๐—ฅ ๐—ง๐—ข๐—ฃ ๐—ง๐—˜๐—”๐—–๐—›๐—˜๐—ฅ๐—ฆ โญ ๐—จ๐—ก๐——๐— ๐—ฌ ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ (๐—ง๐—ก๐— , ๐—ฅ๐——, ๐—ฌ๐—ฆ๐—ฌ, ๐—”๐—–๐—œ๐——, ๐—ฆ๐—ง ๐—ฆ๐—œ๐—ฅ, ๐—œ๐—ก๐—ฆ๐—”๐—™ ๐—”๐—Ÿ๐—œ ๐—ฆ๐—œ๐—ฅ & So On ) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ โญ ๐—ฆ@๐—ฉ@๐—  ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜(๐—”๐—š ๐—ฆ๐—œ๐—ฅ, ๐—”๐—ฆ๐—›๐—œ๐—ฆ๐—› ๐—•๐—”๐—๐—ฃ๐—˜๐—ฌ๐—œโ€ฆ
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โค1๐Ÿคฉ1๐Ÿ†1
Q1.
Assertion (A): For a spontaneous process at constant temperature and pressure, ฮ”G 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 ฮ”G = 0, the system is at equilibrium.
Reason (R): At equilibrium, forward and backward reaction rates are equal


Q3.
Assertion (A): A reaction with ฮ”H < 0 and ฮ”S < 0 is spontaneous at all temperatures.
Reason (R): Decrease in enthalpy always favours spontaneity.



Q5. (Numerical concept)
Assertion (A): If ฮ”H = โˆ’40 kJ and ฮ”S = โˆ’100 J Kโปยน, reaction is spontaneous at low temperature.
Reason (R): Negative ฮ”S disfavors spontaneity at high temperature
๐Ÿ•Š1๐Ÿ˜1๐Ÿณ1
๐ŸŽ‰1๐Ÿ•Š1๐Ÿ’ฏ1
โญ ๐—–๐—œ๐—˜ ๐—ชEE ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ (๐——๐—ก, ๐——๐—, ๐— ๐— ๐—ฆ๐—ง๐—”๐—ฅ, ๐— ๐—ž๐—š & so on) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ

โญ ๐—ข๐—Ÿ๐—— ๐—Ÿ๐—˜๐—–๐—ง๐—จ๐—ฅ๐—˜๐—ฆ ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜โ€” ๐—จ๐—ก๐——๐— ๐—ฌ + ๐—Ÿ๐—ก ๐—ž@๐—ง๐—” + ๐—ฆ@๐—ฉ@๐—  + ๐—ข๐—ง๐—›๐—˜๐—ฅ ๐—ง๐—ข๐—ฃ ๐—ง๐—˜๐—”๐—–๐—›๐—˜๐—ฅ๐—ฆ

โญ ๐—จ๐—ก๐——๐— ๐—ฌ ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ (๐—ง๐—ก๐— , ๐—ฅ๐——, ๐—ฌ๐—ฆ๐—ฌ, ๐—”๐—–๐—œ๐——, ๐—ฆ๐—ง ๐—ฆ๐—œ๐—ฅ, ๐—œ๐—ก๐—ฆ๐—”๐—™ ๐—”๐—Ÿ๐—œ ๐—ฆ๐—œ๐—ฅ & So On ) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ

โญ ๐—ฆ@๐—ฉ@๐—  ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜(๐—”๐—š ๐—ฆ๐—œ๐—ฅ, ๐—”๐—ฆ๐—›๐—œ๐—ฆ๐—› ๐—•๐—”๐—๐—ฃ๐—˜๐—ฌ๐—œ ๐—ฆ๐—œ๐—ฅ, ๐—ฃ๐—”๐—ฅ๐—ฉ๐—˜๐—ญ ๐—ž๐—›๐—”๐—ก, ๐—ฉ๐—ž
๐—ฆ๐—œ๐—ฅ & ๐—ฆ๐—ข ๐—ข๐—ก) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ


โญ ๐—–๐—ข๐—ฃ๐—ฌ๐—ฅ๐—œ๐—š๐—›๐—ง ๐—•๐—”๐—–๐—ž๐—จ๐—ฃ ๐—ข๐—™ ๐—”๐—Ÿ๐—Ÿ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ ๐—ข๐—™ ๐—ง๐—›๐—œ๐—ฆ
โค2๐Ÿ”ฅ1๐Ÿ™1
Chemistry booster series
โญ ๐—–๐—œ๐—˜ ๐—ชEE ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ (๐——๐—ก, ๐——๐—, ๐— ๐— ๐—ฆ๐—ง๐—”๐—ฅ, ๐— ๐—ž๐—š & so on) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ โญ ๐—ข๐—Ÿ๐—— ๐—Ÿ๐—˜๐—–๐—ง๐—จ๐—ฅ๐—˜๐—ฆ ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜โ€” ๐—จ๐—ก๐——๐— ๐—ฌ + ๐—Ÿ๐—ก ๐—ž@๐—ง๐—” + ๐—ฆ@๐—ฉ@๐—  + ๐—ข๐—ง๐—›๐—˜๐—ฅ ๐—ง๐—ข๐—ฃ ๐—ง๐—˜๐—”๐—–๐—›๐—˜๐—ฅ๐—ฆ โญ ๐—จ๐—ก๐——๐— ๐—ฌ ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜ (๐—ง๐—ก๐— , ๐—ฅ๐——, ๐—ฌ๐—ฆ๐—ฌ, ๐—”๐—–๐—œ๐——, ๐—ฆ๐—ง ๐—ฆ๐—œ๐—ฅ, ๐—œ๐—ก๐—ฆ๐—”๐—™ ๐—”๐—Ÿ๐—œ ๐—ฆ๐—œ๐—ฅ & So On ) ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฒ โญ ๐—ฆ@๐—ฉ@๐—  ๐——๐—ฅ๐—˜๐—”๐—  ๐—™๐—ข๐—ฅ๐—š๐—˜(๐—”๐—š ๐—ฆ๐—œ๐—ฅ, ๐—”๐—ฆ๐—›๐—œ๐—ฆ๐—› ๐—•๐—”๐—๐—ฃ๐—˜๐—ฌ๐—œโ€ฆ
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โคโ€๐Ÿ”ฅ4โค2๐Ÿฅฐ1
1๏ธโƒฃ #CHEMICALEQUILIBRIUM
โœ”๏ธ State where forward & reverse reactions occur at same rate
โœ”๏ธ Concentrations of reactants & products become constant
๐Ÿ“Œ Example:
Nโ‚‚ + 3Hโ‚‚ โ‡Œ 2NHโ‚ƒ


2๏ธโƒฃ #EQUILIBRIUMCONSTANT (K)
โœ”๏ธ Ratio of product concentrations to reactant concentrations
โœ”๏ธ Each raised to power of stoichiometric coefficient
๐Ÿ“Œ General reaction:
aA + bB โ‡Œ cC + dD
๐Ÿ“Œ Expression:
Kc = [C]แถœ[D]แตˆ / [A]แตƒ[B]แต‡


3๏ธโƒฃ #TYPESOFEQUILIBRIUMCONSTANT
โœ”๏ธ Kc โ†’ concentration based
โœ”๏ธ Kp โ†’ partial pressure based
๐Ÿ“Œ Relation:
Kp = Kc(RT)โฟ
โœ”๏ธ n = moles of gaseous products โˆ’ moles of gaseous reactants


4๏ธโƒฃ #SIGNIFICANCEOFK
โœ”๏ธ Predicts extent of reaction
โœ”๏ธ Tells position of equilibrium
๐Ÿ“Œ Values:
โœ”๏ธ K โ‰ซ 1 โ†’ Product favoured
โœ”๏ธ K โ‰ช 1 โ†’ Reactant favoured
โœ”๏ธ K โ‰ˆ 1 โ†’ Both present


5๏ธโƒฃ #REACTIONQUOTIENT (Q)
โœ”๏ธ Same expression as K
โœ”๏ธ Calculated at any stage of reaction
๐Ÿ“Œ Comparison:
โœ”๏ธ Q < K โ†’ reaction proceeds forward
โœ”๏ธ Q > K โ†’ reaction proceeds backward
โœ”๏ธ Q = K โ†’ equilibrium


6๏ธโƒฃ #APPLICATION1DIRECTIONOFREACTION
โœ”๏ธ Compare Q with K
โœ”๏ธ Predict spontaneous direction
๐Ÿ“Œ Very important for numericals


7๏ธโƒฃ #APPLICATION2DEGREEOFDISSOCIATION
โœ”๏ธ Used for weak electrolytes
๐Ÿ“Œ Example:
HA โ‡Œ Hโบ + Aโป
K = ฮฑยฒC / (1 โˆ’ ฮฑ)
โœ”๏ธ ฮฑ = degree of dissociation
โœ”๏ธ C = initial concentration


8๏ธโƒฃ #APPLICATION3IONIZATIONOFWEAKELECTROLYTES
โœ”๏ธ Acids & bases have small K value
๐Ÿ“Œ Example:
CHโ‚ƒCOOH โ‡Œ Hโบ + CHโ‚ƒCOOโป
โœ”๏ธ Small K โ†’ weak acid


9๏ธโƒฃ #APPLICATION4CALCULATIONOFCONCENTRATION
โœ”๏ธ Find unknown equilibrium concentration
โœ”๏ธ Used in ICE table method
๐Ÿ“Œ Steps:
โœ”๏ธ Initial concentration
โœ”๏ธ Change
โœ”๏ธ Equilibrium


๐Ÿ”Ÿ #APPLICATION5EFFECTOFCHANGINGCONDITIONS
โœ”๏ธ Temperature change affects K
โœ”๏ธ Concentration & pressure do NOT change K
๐Ÿ“Œ Only temperature changes K value


1๏ธโƒฃ1๏ธโƒฃ #EFFECTOFTEMPERATURE
โœ”๏ธ Endothermic reaction:
Temperature โ†‘ โ†’ K โ†‘
โœ”๏ธ Exothermic reaction:
Temperature โ†‘ โ†’ K โ†“


1๏ธโƒฃ2๏ธโƒฃ #RELATIONWITHGIBBSFREEENERGY
๐Ÿ“Œ Formula:
ฮ”Gยฐ = โˆ’RT ln K
โœ”๏ธ ฮ”Gยฐ < 0 โ†’ K > 1 (spontaneous)
โœ”๏ธ ฮ”Gยฐ > 0 โ†’ K < 1


1๏ธโƒฃ3๏ธโƒฃ #HETEROGENEOUSEQUILIBRIUM
โœ”๏ธ Solids & liquids not included in K
๐Ÿ“Œ Example:
CaCOโ‚ƒ(s) โ‡Œ CaO(s) + COโ‚‚(g)
Kp = P(COโ‚‚)


1๏ธโƒฃ4๏ธโƒฃ #REVERSINGREACTION
โœ”๏ธ K(reverse) = 1 / K(forward)


1๏ธโƒฃ5๏ธโƒฃ #MULTIPLYINGREACTION
โœ”๏ธ If reaction multiplied by n
โœ”๏ธ New K = Kโฟ


1๏ธโƒฃ6๏ธโƒฃ #NEETโš ๏ธ
โœ”๏ธ K depends only on temperature
โœ”๏ธ Catalyst does not change K
โœ”๏ธ Pure solids not included
โœ”๏ธ Units of K depend on reaction


1๏ธโƒฃ7๏ธโƒฃ #ONELINEREVISION
โœ”๏ธ K predicts extent of reaction
โœ”๏ธ Q vs K gives direction
โœ”๏ธ Only temperature affects K
โœ”๏ธ Kpโ€“Kc relation important
โค3๐Ÿ‘2๐Ÿ‘Œ2๐Ÿ’ฏ1
โƒฃ #SOLUBILITYPRODUCT
โœ”๏ธ Solubility product = product of molar concentrations of ions in saturated solution
โœ”๏ธ Each concentration raised to power of its stoichiometric coefficient
๐Ÿ“Œ For salt: Aโ‚“Bแตง
Ksp = [Aโบ]หฃ [Bโป]สธ


2๏ธโƒฃ #CONDITIONOFAPPLICABILITY
โœ”๏ธ Salt must be sparingly soluble
โœ”๏ธ Solution must be saturated
โœ”๏ธ At constant temperature

.
3๏ธโƒฃ #IONICDISSOCIATION
โœ”๏ธ AB(s) โ‡Œ Aโบ + Bโป
โœ”๏ธ Aโ‚‚B(s) โ‡Œ 2Aโบ + Bยฒโป
โœ”๏ธ ABโ‚‚(s) โ‡Œ Aโบ + 2Bโป
.

4๏ธโƒฃ #MOLARSOLUBILITY (S)
โœ”๏ธ Molar solubility = moles dissolved per litre to form saturated solution
๐Ÿ“Œ Units: mol Lโปยน


โญโญ5๏ธโƒฃ #KspINTERMSSOLUBILITY (VERY IMP )

5๏ธโƒฃ1๏ธโƒฃ For AB
AB โ‡Œ Aโบ + Bโป
Ksp = Sยฒ
S = โˆšKsp

5๏ธโƒฃ2๏ธโƒฃ For Aโ‚‚B
Aโ‚‚B โ‡Œ 2Aโบ + Bยฒโป
Ksp = (2S)ยฒ(S) = 4Sยณ
S = (Ksp / 4)ยนแŸยณ

5๏ธโƒฃ3๏ธโƒฃ For ABโ‚‚
ABโ‚‚ โ‡Œ Aโบ + 2Bโป
Ksp = S(2S)ยฒ = 4Sยณ
S = (Ksp / 4)ยนแŸยณ

5๏ธโƒฃ4๏ธโƒฃ For Aโ‚ƒB
Aโ‚ƒB โ‡Œ 3Aโบ + Bยณโป
Ksp = (3S)ยณ(S) = 27Sโด


6๏ธโƒฃ #IONICPRODUCT (IP)
โœ”๏ธ IP = product of ionic concentrations at any instant
๐Ÿ“Œ Comparison:
โœ”๏ธ IP < Ksp โ†’ Unsaturated
โœ”๏ธ IP = Ksp โ†’ Saturated
โœ”๏ธ IP > Ksp โ†’ Precipitation
.
7๏ธโƒฃ #COMMONIONEFFECT (NEET )
โœ”๏ธ Solubility decreases in presence of common ion
๐Ÿ“Œ Example:
AgCl solubility โ†“ in NaCl solution
๐Ÿ“Œ Reason: Equilibrium shifts backward


8๏ธโƒฃ #EFFECTOFPHONCOMMONION
โœ”๏ธ Solubility increases if no common ion present


9๏ธโƒฃ #SELECTIVEPRECIPITATION
โœ”๏ธ Salt with lower Ksp precipitates first
๐Ÿ“Œ Used in qualitative analysis


๐Ÿ”Ÿ #RELATIONBETWEENSOLUBILITYANDKsp
โœ”๏ธ Higher Ksp โ‰  higher solubility always
โœ”๏ธ Depends on stoichiometry of salt


1๏ธโƒฃ1๏ธโƒฃ #SOLUBILITYINPRESENCEOFCOMMONION
For AB in presence of Bโป concentration = C
Ksp = S ร— C
S = Ksp / C
๐Ÿ“Œ Used in buffer & salt solutions


1๏ธโƒฃ2๏ธโƒฃ #SOLUBILITYINPRESENCEOFPH
โœ”๏ธ For salts of weak acids โ†’ solubility increases in acidic medium
โœ”๏ธ For salts of weak bases โ†’ solubility increases in basic medium
๐Ÿ“Œ Example:
CaCOโ‚ƒ dissolves more in acidic solution


1๏ธโƒฃ3๏ธโƒฃ #TEMPERATUREEFFECT
โœ”๏ธ Ksp increases with temperature (usually)
โœ”๏ธ Endothermic dissolution favoured


1๏ธโƒฃ4๏ธโƒฃ #UNITOFKsp
โœ”๏ธ Depends on stoichiometry
โœ”๏ธ No fixed unit
๐Ÿ“Œ NEET note: Ksp has no unit


1๏ธโƒฃ5๏ธโƒฃ #COMPARISONOFKspVALUES
โœ”๏ธ Compare only salts with same formula type
โœ”๏ธ Otherwise comparison invalid


1๏ธโƒฃ6๏ธโƒฃ #PRECIPITATIONCONDITION
โœ”๏ธ Precipitation starts when IP just exceeds Ksp


1๏ธโƒฃ7๏ธโƒฃ #SOLUBILITYORDER
โœ”๏ธ Lower Ksp โ†’ lower solubility (for same type salts)


1๏ธโƒฃ8๏ธโƒฃ #NEETโš ๏ธTRAPS
โœ”๏ธ Ksp valid only for saturated solution
โœ”๏ธ Ksp โ‰  solubility
โœ”๏ธ Common ion reduces solubility
โœ”๏ธ Ksp independent of initial concentration
โœ”๏ธ Compare Ksp only at same temperature


1๏ธโƒฃ9๏ธโƒฃ #NUMERICALSHORTCUT
โœ”๏ธ If Ksp = 10โปยนโฐ for AB
S โ‰ˆ 10โปโต
โœ”๏ธ If Ksp = 4ร—10โปยนยฒ for ABโ‚‚
S โ‰ˆ 10โปโด


2๏ธโƒฃ0๏ธโƒฃ #ONELINEREVISION
โœ”๏ธ Ksp = ionic product at saturation
โœ”๏ธ Precipitation when IP > Ksp
โœ”๏ธ Common ion โ†“ solubility
โœ”๏ธ Same Ksp โ‰  same solubility
โค2๐Ÿ’ฏ2๐Ÿ˜Ž1
Q1
Assertion (A): Solubility of AgCl decreases on addition of NaCl.
Reason (R): Addition of NaCl increases concentration of Clโป 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): Hโบ ions react with SOโ‚„ยฒโป ions to form HSOโ‚„โป.


Q5
Assertion (A): Two salts having same Ksp may have different solubilities.
Reason (R): Solubility depends on number of ions produced on dissociation

.
โค1๐ŸŽ‰1
1๏ธโƒฃ #WEAKELECTROLYTES
โœ”๏ธ Weak acids & weak bases ionise partially in aqueous solution
โœ”๏ธ Establish equilibrium between ionised & unionised form
๐Ÿ“Œ Examples:
โœ”๏ธ Weak acid โ†’ CHโ‚ƒCOOH
โœ”๏ธ Weak base โ†’ NHโ‚„OH


2๏ธโƒฃ #IONISATIONOFWEAKACID
โœ”๏ธ Partial dissociation in water
๐Ÿ“Œ General reaction:
HA + Hโ‚‚O โ‡Œ Hโ‚ƒOโบ + Aโป
๐Ÿ“Œ Example:
CHโ‚ƒCOOH + Hโ‚‚O โ‡Œ Hโ‚ƒOโบ + CHโ‚ƒCOOโป


3๏ธโƒฃ #ACIDDISSOCIATIONCONSTANT (Ka)
โœ”๏ธ Measure of strength of weak acid
โœ”๏ธ Higher Ka โ†’ stronger acid
๐Ÿ“Œ Expression:
Ka = [Hโบ][Aโป] / [HA]
โœ”๏ธ Unit: mol Lโปยน


4๏ธโƒฃ #DEGREEOFIONISATION (ฮฑ)
โœ”๏ธ Fraction of total molecules ionised
๐Ÿ“Œ Formula:
ฮฑ = Number of molecules ionised / Total molecules
โœ”๏ธ For weak acids โ†’ ฮฑ โ‰ช 1


5๏ธโƒฃ #RELATIONBETWEENKaANDฮฑ (NEET FAV )
For weak acid of concentration C:
๐Ÿ“Œ Formula:
Ka = Cฮฑยฒ
๐Ÿ“Œ Therefore:
ฮฑ = โˆš(Ka / C)
โœ”๏ธ Ionisation increases on dilution


6๏ธโƒฃ #pKaCONCEPT
โœ”๏ธ pKa = โ€“log Ka
โœ”๏ธ Lower pKa โ†’ stronger acid
๐Ÿ“Œ Relation:
Strong acid โ†’ small pKa
Weak acid โ†’ large pKa


7๏ธโƒฃ #pHOFWEAKACID
For weak acid of concentration C:
๐Ÿ“Œ Formula:
[Hโบ] = โˆš(Ka ร— C)
๐Ÿ“Œ pH formula:
pH = ยฝ ( pKa โ€“ log C )
โœ”๏ธ Very important for numericals


8๏ธโƒฃ #IONISATIONOFWEAKBASE
โœ”๏ธ Partial dissociation in water
๐Ÿ“Œ General reaction:
BOH โ‡Œ Bโบ + OHโป
๐Ÿ“Œ Example:
NHโ‚„OH โ‡Œ NHโ‚„โบ + OHโป


9๏ธโƒฃ #BASEDISSOCIATIONCONSTANT (Kb)
โœ”๏ธ Measure of strength of weak base
โœ”๏ธ Higher Kb โ†’ stronger base
๐Ÿ“Œ Expression:
Kb = [Bโบ][OHโป] / [BOH]


๐Ÿ”Ÿ #RELATIONBETWEENKbANDฮฑ
For weak base of concentration C:
๐Ÿ“Œ Formula:
Kb = Cฮฑยฒ
๐Ÿ“Œ Therefore:
ฮฑ = โˆš(Kb / C)


1๏ธโƒฃ1๏ธโƒฃ #pKbCONCEPT
โœ”๏ธ pKb = โ€“log Kb
โœ”๏ธ Lower pKb โ†’ stronger base


1๏ธโƒฃ2๏ธโƒฃ #pHOFWEAKBASE
For weak base of concentration C:
๐Ÿ“Œ [OHโป] = โˆš(Kb ร— C)
๐Ÿ“Œ pOH formula:
pOH = ยฝ ( pKb โ€“ log C )
๐Ÿ“Œ pH = 14 โ€“ pOH


1๏ธโƒฃ3๏ธโƒฃ #DILUTIONEFFECT (VERY IMP ๐Ÿ”ฅ)
โœ”๏ธ On dilution โ†’ degree of ionisation increases
โœ”๏ธ But total ions per unit volume decrease
๐Ÿ“Œ Ostwaldโ€™s dilution law applies


1๏ธโƒฃ4๏ธโƒฃ #COMMONIONEFFECT
โœ”๏ธ Ionisation of weak electrolyte decreases
โœ”๏ธ Presence of common ion shifts equilibrium backward
๐Ÿ“Œ Example:
CHโ‚ƒCOOH + CHโ‚ƒCOONa โ†’ ionisation decreases


1๏ธโƒฃ5๏ธโƒฃ #WEAKACIDVSWEAKBASE
โœ”๏ธ Weak acid โ†’ Hโบ producing
โœ”๏ธ Weak base โ†’ OHโป producing
โœ”๏ธ Both show partial ionisation


1๏ธโƒฃ6๏ธโƒฃ #NEETโš ๏ธKEYPOINTS
โœ”๏ธ Ka & Kb are temperature dependent
โœ”๏ธ ฮฑ increases with dilution
โœ”๏ธ pH of weak acid > strong acid (same concentration)
โœ”๏ธ pH of weak base < strong base (same concentration)


1๏ธโƒฃ7๏ธโƒฃ #ONELINEREVISION
โœ”๏ธ Weak electrolytes ionise partially
โœ”๏ธ Ka = Cฮฑยฒ
โœ”๏ธ [Hโบ] = โˆš(Ka ร— C)
โœ”๏ธ pH weak acid = ยฝ (pKa โ€“ log C)
โœ”๏ธ Dilution increases ionisation
โค5๐Ÿ’ฏ2๐Ÿ”ฅ1
1๏ธโƒฃ #REDOXREACTION
โœ”๏ธ Redox reaction = reaction involving simultaneous oxidation and reduction
โœ”๏ธ Oxidation โ†’ loss of electrons
โœ”๏ธ Reduction โ†’ gain of electrons
๐Ÿ“Œ Example:
Zn + Cuยฒโบ โ†’ Znยฒโบ + Cu
โœ”๏ธ Zn โ†’ Znยฒโบ + 2eโป (Oxidation)
โœ”๏ธ Cuยฒโบ + 2eโป โ†’ Cu (Reduction)


2๏ธโƒฃ #OXIDATIONNUMBERCONCEPT
โœ”๏ธ Oxidation number (ON) = hypothetical charge if all bonds ionic
โœ”๏ธ Increase in ON โ†’ oxidation
โœ”๏ธ Decrease in ON โ†’ reduction
๐Ÿ“Œ Rules:
โœ”๏ธ Element in free state โ†’ ON = 0
โœ”๏ธ Monatomic ion โ†’ ON = charge
โœ”๏ธ Oxygen โ†’ usually โ€“2
โœ”๏ธ Hydrogen โ†’ usually +1
โœ”๏ธ Sum of ONs in molecule โ†’ 0
โœ”๏ธ Sum of ONs in polyatomic ion โ†’ ion charge


3๏ธโƒฃ #TYPESOFREDOXREACTIONS
โœ”๏ธ Combination reaction โ†’ A + B โ†’ AB
โœ”๏ธ Decomposition โ†’ AB โ†’ A + B
โœ”๏ธ Displacement โ†’ A + BC โ†’ AC + B
โœ”๏ธ Disproportionation โ†’ X โ†’ Xโฟโบ + Xแตโป
๐Ÿ“Œ Example:
2Hโ‚‚Oโ‚‚ โ†’ 2Hโ‚‚O + Oโ‚‚
โœ”๏ธ O in Hโ‚‚Oโ‚‚: โ€“1 โ†’ 0 & โ€“2 (disproportionation)


4๏ธโƒฃ #OXIDISINGAGENT
โœ”๏ธ Substance that accepts electrons
โœ”๏ธ Causes oxidation of other species
๐Ÿ“Œ Example:
โœ”๏ธ Cuยฒโบ in Zn + Cuยฒโบ โ†’ Cuยฒโบ is oxidising agent


5๏ธโƒฃ #REDUCINGAGENT
โœ”๏ธ Substance that donates electrons
โœ”๏ธ Causes reduction of other species
๐Ÿ“Œ Example:
โœ”๏ธ Zn in Zn + Cuยฒโบ โ†’ Zn is reducing agent


6๏ธโƒฃ #ELECTRONBALANCEMETHOD (NEET FAV )
โœ”๏ธ Step 1 โ†’ Write oxidation & reduction half-reactions
โœ”๏ธ Step 2 โ†’ Balance atoms other than O & H
โœ”๏ธ Step 3 โ†’ Balance O by Hโ‚‚O
โœ”๏ธ Step 4 โ†’ Balance H by Hโบ (acidic) or OHโป (basic)
โœ”๏ธ Step 5 โ†’ Balance electrons
โœ”๏ธ Step 6 โ†’ Combine half-reactions


7๏ธโƒฃ #IONICEQUATIONEXAMPLE
โœ”๏ธ Feยฒโบ + Crโ‚‚Oโ‚‡ยฒโป โ†’ Feยณโบ + Crยณโบ (acidic medium)
๐Ÿ“Œ Half-reactions:
Feยฒโบ โ†’ Feยณโบ + eโป
Crโ‚‚Oโ‚‡ยฒโป + 14Hโบ + 6eโป โ†’ 2Crยณโบ + 7Hโ‚‚O
๐Ÿ“Œ Multiply Fe reaction by 6 โ†’ 6Feยฒโบ โ†’ 6Feยณโบ + 6eโป
๐Ÿ“Œ Combine โ†’ 6Feยฒโบ + Crโ‚‚Oโ‚‡ยฒโป + 14Hโบ โ†’ 6Feยณโบ + 2Crยณโบ + 7Hโ‚‚O


8๏ธโƒฃ #DISPROPORTIONATIONREACTIONS
โœ”๏ธ Same element undergoes oxidation & reduction simultaneously
๐Ÿ“Œ Example:
3Clโ‚‚ + 6OHโป โ†’ 5Clโป + ClOโ‚ƒโป + 3Hโ‚‚O
โœ”๏ธ Cl โ†’ โ€“1 & +5


9๏ธโƒฃ #NEETโš ๏ธKEYPOINTS
โœ”๏ธ Redox can occur in acidic or basic medium
โœ”๏ธ Use oxidation number method for quick identification
โœ”๏ธ Disproportionation = special redox with same element
โœ”๏ธ Oxidising & reducing agents always appear on opposite sides


1๏ธโƒฃ0๏ธโƒฃ #ONELINEREVISION
โœ”๏ธ Redox = Oxidation + Reduction
โœ”๏ธ Oxidation โ†’ loss eโป, ON โ†‘
โœ”๏ธ Reduction โ†’ gain eโป, ON โ†“
โœ”๏ธ Oxidising agent โ†’ gains eโป
โœ”๏ธ Reducing agent โ†’ loses eโป
โœ”๏ธ Use half-reaction method for balancing
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โค2๐Ÿณ1
๐Ÿ†2๐Ÿ™1
All cyclic compound โค
โค2๐Ÿ‘2๐Ÿ’ฏ2๐Ÿ”ฅ1๐Ÿซก1
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 โญEA : 2nd period se 3rd vale ki hmesha jyada
Highest Cl
Oxygen family M O last m
โค2๐Ÿ”ฅ2๐Ÿ˜˜2๐Ÿ’ฏ1
1๏ธโƒฃ #CARBONFAMILY
โœ”๏ธ Group number โ†’ 14
โœ”๏ธ General electronic configuration:
๐Ÿ“Œ nsยฒ npยฒ
โœ”๏ธ Members:
โœ”๏ธ Carbon (C)
โœ”๏ธ Silicon (Si)
โœ”๏ธ Germanium (Ge)
โœ”๏ธ Tin (Sn)
โœ”๏ธ Lead (Pb)


2๏ธโƒฃ #POSITIONINPERIODICTABLE
โœ”๏ธ Lies between Boron family (13) & Nitrogen family (15)
โœ”๏ธ First group containing non-metal โ†’ metalloid โ†’ metal trend
๐Ÿ“Œ Nature trend:
โœ”๏ธ C โ†’ Non-metal
โœ”๏ธ Si, Ge โ†’ Metalloids
โœ”๏ธ Sn, Pb โ†’ Metals


3๏ธโƒฃ #ATOMICANDPHYSICALPROPERTIES
โœ”๏ธ Atomic radius โ†‘ down the group
โœ”๏ธ Ionisation enthalpy โ†“ down the group
โœ”๏ธ Electronegativity โ†“ down the group
๐Ÿ“Œ Density:
โœ”๏ธ Increases downwards (exception: Pb irregularity)


4๏ธโƒฃ #COVALENTCHARACTER
โœ”๏ธ Strong covalent bonding (especially C, Si)
โœ”๏ธ Due to:
โœ”๏ธ Small size
โœ”๏ธ High electronegativity
๐Ÿ“Œ Carbon shows maximum covalency (4)


5๏ธโƒฃ #OXIDATIONSTATES โญ VERY IMP
โœ”๏ธ Common oxidation states:
โœ”๏ธ +4 and +2
๐Ÿ“Œ Stability trend:
โœ”๏ธ +4 stable for C, Si
โœ”๏ธ +2 stability โ†‘ down the group
๐Ÿ“Œ Reason:
โœ”๏ธ Inert pair effect (Sn, Pb)
๐Ÿ“Œ Examples:
โœ”๏ธ COโ‚‚ โ†’ +4
โœ”๏ธ CO โ†’ +2
โœ”๏ธ SnClโ‚‚ (+2) more stable than SnClโ‚„


6๏ธโƒฃ #INERTPAIREFFECT
โœ”๏ธ Poor shielding of d & f electrons
โœ”๏ธ nsยฒ electrons less available for bonding
๐Ÿ“Œ Order:
C < Si < Ge < Sn < Pb
โœ”๏ธ Pb shows strongest inert pair effect


7๏ธโƒฃ #CATABENATION (NEET FAV )
โœ”๏ธ Ability to form long chains
๐Ÿ“Œ Order:
C >>> Si > Ge > Sn > Pb
๐Ÿ“Œ Reason:
โœ”๏ธ Strong Cโ€“C bond
โœ”๏ธ Small atomic size
โœ”๏ธ Carbon forms:
โœ”๏ธ Straight chains
โœ”๏ธ Branched chains
โœ”๏ธ Rings


8๏ธโƒฃ #ALLOTROPY
โœ”๏ธ Carbon shows extensive allotropy
๐Ÿ“Œ Allotropes of carbon:
โœ”๏ธ Diamond โ†’ hardest, spยณ
โœ”๏ธ Graphite โ†’ conductor, spยฒ
โœ”๏ธ Fullerene (Cโ‚†โ‚€)
โœ”๏ธ Si, Ge show limited allotropy


9๏ธโƒฃ #HYDRIDES
โœ”๏ธ General formula: MHโ‚„
๐Ÿ“Œ Examples:
โœ”๏ธ CHโ‚„ โ†’ Methane
โœ”๏ธ SiHโ‚„ โ†’ Silane
๐Ÿ“Œ Stability:
CHโ‚„ > SiHโ‚„ > GeHโ‚„ > SnHโ‚„
โœ”๏ธ Reducing character โ†‘ down group


1๏ธโƒฃ0๏ธโƒฃ #HALIDES
โœ”๏ธ General formula: MXโ‚„
๐Ÿ“Œ Examples:
โœ”๏ธ CClโ‚„
โœ”๏ธ SiClโ‚„
๐Ÿ“Œ Hydrolysis:
โœ”๏ธ CClโ‚„ โ†’ no hydrolysis
โœ”๏ธ SiClโ‚„ โ†’ hydrolyses easily
๐Ÿ“Œ Reason:
โœ”๏ธ Availability of vacant d-orbitals in Si


1๏ธโƒฃ1๏ธโƒฃ #OXIDES
โœ”๏ธ General formula: MOโ‚‚
๐Ÿ“Œ Nature:
โœ”๏ธ COโ‚‚ โ†’ acidic
โœ”๏ธ SiOโ‚‚ โ†’ weakly acidic
โœ”๏ธ SnOโ‚‚, PbOโ‚‚ โ†’ amphoteric
๐Ÿ“Œ Acidity โ†“ down the group


1๏ธโƒฃ2๏ธโƒฃ #ANOMALOUSBEHAVIOUROFCARBON
โœ”๏ธ Small size
โœ”๏ธ High electronegativity
โœ”๏ธ Strong pฯ€โ€“pฯ€ bonding
โœ”๏ธ Maximum catenation
โœ”๏ธ No d-orbitals
๐Ÿ“Œ Hence carbon differs from rest of group


1๏ธโƒฃ3๏ธโƒฃ #USES (NEET RELEVANT)
โœ”๏ธ Carbon โ†’ fuels, organic compounds
โœ”๏ธ Silicon โ†’ semiconductors, glass
โœ”๏ธ Tin โ†’ coating (tin cans)
โœ”๏ธ Lead โ†’ batteries, radiation shielding


1๏ธโƒฃ4๏ธโƒฃ #NEETKEYPOINTS
โœ”๏ธ +2 oxidation state stability โ†‘ down group
โœ”๏ธ Inert pair effect strongest in Pb
โœ”๏ธ Carbon shows maximum catenation
โœ”๏ธ COโ‚‚ acidic, PbOโ‚‚ amphoteric


1๏ธโƒฃ5๏ธโƒฃ #ONELINEREVISION
โœ”๏ธ Group 14 โ†’ nsยฒ npยฒ
โœ”๏ธ C non-metal โ†’ Pb metal
โœ”๏ธ Oxidation states +4, +2
โœ”๏ธ Inert pair effect important
โœ”๏ธ Carbon is exceptional
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