Thermodynamics and Thermochemistry
    1.0 Introduction to Thermodynamics
    2.0 Thermodynamic Processes
    3.0 Heat $(Q)$
    4.0 Work $(W)$
    5.0 Internal Energy
    6.0 Zeroth Law of Thermodynamic
    7.0 First Law of Thermodynamics
    8.0 Heat Capacity
    9.0 Enthalpy $(H)$ or Heat Content
    10.0 Significance of $?H$ and $?E$
    11.0 Relationship Between $?H$ and $?E$
    12.0 Standard Enthalpy of Reaction
    13.0 Law of Thermodynamics
    14.0 Bond Energy or Bond Enthalpies
    15.0 Second Law of Thermodynamic
    16.0 Entropy (S)
    17.0 Spontaneous Processes
    18.0 Free Energy (G)
    19.0 Enthalpy, Entropy, Free Energy Changes and The Nature of Process
    20.0 Standard Free Energy Change
    21.0 Coupled Reactions
    22.0 Third Law of Thermodynamic
    23.0 Important Facts

16.1 Some Important points Related to Entropy

(1) Entropy change, $\Delta S = S\left( {Final\;state} \right) - S\left( {Intial\;state} \right)$

(2) $\Delta S = $ Increase in entropy of positive system.

(3) $\Delta S = $ Decrease in entropy of negative system.

(4) When a solute gets dissolved in the solvent, the entropy increases.

(5) When the number of gaseous products increase in a chemical reaction, the entropy also increases.

For example,

$${\left( {N{H_4}} \right)_2}S(s) \to 2N{H_3}(g) + {H_2}S(g)$$

(6) $N{H_3}(g) + HCl(g) \to N{H_4}Cl(s)$ Entropy is decreasing.

(7) For reaction, change in entropy $\Delta S = $ Sum of entropies of the product $-$ Sum of entropy of the reactants.

(8) Unite of entropy is joule $kelvi{n^{ - 1}}\;mol{e^{ - 1}}$

(9) At equilibrium, $\Delta S = 0$

(10) Entropy change in an isothermal reversible expansion of a gas

$$\Delta S = 2.303\;nR\;\log \frac{{{V_2}}}{{{V_1}}}$$

${{V_2}}$ and ${{V_1}}$ are final and initial volumes of the gas.

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