Complete NEET prep for Thermodynamics: NCERT-aligned notes on enthalpy, entropy, Gibbs free energy, laws of thermodynamics, Hess's law, standard enthalpies, and spontaneity. PYQs with solutions. Built for NEET 2027.
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System, surroundings, boundary: open, closed, and isolated systems
State functions vs path functions: internal energy (U), enthalpy (H), entropy (S), Gibbs energy (G)
First law: ΔU = q + w; at constant pressure: ΔH = q_p
Heat capacity: C_v and C_p; relationship C_p − C_v = R for ideal gases
Standard enthalpy of formation, combustion, neutralisation, atomisation, and bond dissociation
Hess's law of constant heat summation and its applications
Born-Haber cycle for ionic solids
Second law of thermodynamics: entropy as a measure of disorder
Gibbs free energy: ΔG = ΔH − TΔS; criteria for spontaneity at constant T and P
ΔG° = −RT ln K; relationship between Gibbs energy and equilibrium constant
10 questions from Thermodynamics across the last 5 NEET papers.
NEET 2024
2
questions
NEET 2023
2
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NEET 2022
2
questions
NEET 2021
2
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NEET 2020
2
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ΔU is the change in internal energy at constant volume. ΔH is the change in enthalpy at constant pressure (which is the heat exchanged in most lab reactions). They are related by ΔH = ΔU + Δn_g RT, where Δn_g is the change in moles of gas. For reactions with no gaseous species or no change in moles of gas, ΔH ≈ ΔU.
Write the target reaction at the top. Look at the given reactions and adjust them (reverse, multiply, or divide) so that when you add them together, you get the target. For each operation: reversing changes the sign of ΔH; multiplying by n multiplies ΔH by n. The ΔH of the target reaction is the algebraic sum of the ΔH values of the adjusted reactions.
A reaction is spontaneous when ΔG < 0 (where ΔG = ΔH − TΔS). If ΔH < 0 and ΔS > 0: always spontaneous. If ΔH > 0 and ΔS < 0: never spontaneous. If ΔH < 0 and ΔS < 0: spontaneous at low temperature (ΔH term dominates). If ΔH > 0 and ΔS > 0: spontaneous at high temperature (TΔS term dominates). The crossover temperature is T = ΔH/ΔS.
For a strong acid + strong base, the net ionic reaction is just H⁺(aq) + OH⁻(aq) → H₂O(l), releasing about −57.1 kJ/mol. When a weak acid is used (e.g., acetic acid), some energy must first be used to ionise the weak acid (ionisation is endothermic). This reduces the net heat released, making ΔH_neutralisation less negative (say −55.2 kJ/mol for acetic acid + NaOH).
ΔG° = −RT ln K. If ΔG° is negative (large negative value), K is greater than 1, meaning products are favoured at equilibrium. If ΔG° is positive, K is less than 1, reactants are favoured. At equilibrium, ΔG = 0 (not ΔG°). ΔG° is the standard Gibbs energy change (all species at 1 bar, 298 K); ΔG = 0 describes the equilibrium condition under actual concentrations.
A positive ΔS means the products are more disordered (have more randomness) than the reactants. This happens when: the number of moles of gas increases in the reaction; a solid dissolves into ions; a liquid evaporates; a solid melts. ΔS > 0 makes ΔG more negative, favouring spontaneity, especially at high temperatures.
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