Thermo Dynamics
Thermo Dynamics
Thermo Dynamics
Atomic Structure
Shilpi Kaushik
NIT Jalandhar
Next Chemistry Session Details
Date 9 Dec
Time 12:00 PM
t.me/vedantumath1
New JEE 2024
1. Heat Capacity
2. Calculation of work (in diff processes)
3. Entropy
Let’s see the Mind Map
First Law of thermodynamics
ΔU = q + W
Where,
👉 ΔU = change in internal energy of the system.
👉 q = algebraic sum of heat transfer between system
and surroundings.
👉 W = work interaction of the system with
its surroundings.
Work done on the Heat absorbed
system +q
+W
System
Work done by the
system Heat released
-q
-W
Types of Process
Isothermal ΔT = 0, ΔU = 0, q=
-W
Isobaric ΔP = 0
Isochoric ΔV = 0, W = 0, ΔU =q
Adiabatic q = 0, ΔU =W
ENTHALPY (H)
Mathematically,
H = U + PV
Molar Heat Capacity (Cm)
q = n Cm ΔT
👉 It is an Intensive property
👉 It is a Path function
Important result
Cp - CV =
R
Work for different processes
Molar Heat Capacity at Constant Volume (Cv)
qv = ΔU = nCv ΔT
qp = ΔH = nCp ΔT
Relation between Cp and Cv for Ideal gas
Cp - Cv =R
SECOND LAW OF THERMODYNAMICS
𝚫S = qrev /T
SECOND LAW OF THERMODYNAMICS
𝚫S = 𝚫S + 𝚫S >0
total system surrounding
SECOND LAW OF THERMODYNAMICS
General expression
Isothermal process
Isobaric process
Isochoric process
Gibbs Free energy
At a constant temperature:
𝚫Gsys = 𝚫H – T𝚫Ssys
Gibbs Free energy
Gibbs Free energy
𝚫H < 0 𝚫H > 0
Spontaneous
𝚫S > 0 Spontaneous At high
temperature
Spontaneous
Non-
𝚫S < 0 At low
Spontaneous
temperature
Hess’s Law
The overall enthalpy of a chemical
process is independent of the path taken
Type 2
Type 3
Type 4
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8th Jan 2020-(Shift 1)