1. Dynamic equilibrium
At equilibrium, microscopic forward and reverse changes continue at equal rates, so bulk composition remains constant. Equilibrium is not a state where reaction has stopped.
NEET · Chemistry
Own the complete official Unit 6 architecture: physical and chemical equilibrium, law-of-mass-action expressions, Kc/Kp relationships, reaction quotient, Gibbs relationship, Le Chatelier principle and the bridge to the focused Ionic Equilibrium child route.
In short
Equilibrium is dynamic: forward and reverse processes continue while macroscopic composition remains constant under fixed conditions. Write the balanced reaction first, construct the appropriate equilibrium expression, compare Q with K to infer direction, and use Le Chatelier reasoning only after identifying which variable is externally changed. Ionic Equilibrium is part of this official unit but its detailed pH/buffer/Ksp calculations live on the focused child page.
At equilibrium, microscopic forward and reverse changes continue at equal rates, so bulk composition remains constant. Equilibrium is not a state where reaction has stopped.
For a balanced reaction, the equilibrium expression is built from activities; routine NEET concentration/partial-pressure models use the specified powers from stoichiometric coefficients. Pure solids and pure liquids are omitted from variable concentration/pressure terms in the usual heterogeneous-equilibrium treatment because their activities are treated as unity.
Kc uses concentration-form quantities, while Kp uses partial-pressure-form quantities for gaseous species. The numerical value of an equilibrium constant depends on temperature and on the reaction as written.
The reaction quotient Q has the same algebraic form as K but uses the current composition. For the forward reaction:
For an ideal-gas reaction model, Kp = Kc (RT)^Delta n_g, where Delta n_g is gaseous-product stoichiometric moles minus gaseous-reactant stoichiometric moles. Use a consistent standard/concentration convention; do not treat K dimensions casually when moving beyond textbook concentration models.
Delta G = Delta G° + RT ln Q. At equilibrium Delta G=0 and Q=K, giving Delta G° = -RT ln K. This connects thermodynamic driving force to equilibrium position without saying that a large K makes the reaction fast.
A system responds to an imposed change by shifting in the direction that tends to oppose that disturbance. Concentration changes affect Q immediately. Pressure/volume changes matter particularly for gaseous equilibria and depend on Delta n_g. A catalyst changes rates of approach to equilibrium but does not change K or equilibrium composition. Temperature changes K because heat effects change the thermodynamic balance.
K expression from balanced equation: Powers from stoichiometric coefficients. Including pure solid/liquid concentration terms as variables.
K expression from balanced equation
Use when — Including pure solid/liquid concentration terms as variables.
Q same form as K: Current, not equilibrium, composition. Comparing Q for one written reaction with K for its reverse.
Q same form as K
Use when — Comparing Q for one written reaction with K for its reverse.
Q<K forward; Q>K reverse: Same T and same reaction definition. Calling Q a new equilibrium constant.
Q<K forward; Q>K reverse
Use when — Calling Q a new equilibrium constant.
Kp = Kc(RT)^Delta n_g: Ideal-gas relation; T K. Counting solids/liquids in Delta n_g.
Kp = Kc(RT)^Delta n_g
Use when — Counting solids/liquids in Delta n_g.
Delta G = Delta G° + RT ln Q: Compatible energy/R units; T K. Using log10 without factor.
Delta G = Delta G° + RT ln Q
Use when — Using log10 without factor.
Delta G° = -RT ln K: Standard-state equilibrium relation. Inferring reaction speed from K.
Delta G° = -RT ln K
Use when — Inferring reaction speed from K.
Original NEET-style item: For N2O4(g) <=> 2NO2(g), express the relationship between Kp and Kc using the ideal-gas textbook relation.
Reasoning: Delta n_g = 2 - 1 = 1. Therefore Kp = Kc(RT)^1 = Kc RT. The exponent comes only from gaseous stoichiometric coefficients.
Thinks equilibrium means reactions stop
Knowledge gapWhy it happens
Preparation Intelligence classification: Knowledge Gap.
How it is corrected
Rebuild equal forward/reverse rate concept.
Forgets Q/K direction rule
Recall gapWhy it happens
Preparation Intelligence classification: Recall Gap.
How it is corrected
Retrieve Q<K forward, Q>K reverse with reaction orientation.
Counts liquid/solid terms in Delta n_g
Execution errorWhy it happens
Preparation Intelligence classification: Execution Error.
How it is corrected
Count gaseous stoichiometric coefficients only.
Uses pressure change to predict shift without checking gaseous mole difference
Decision / selection errorWhy it happens
Preparation Intelligence classification: Decision / Selection Error.
How it is corrected
Calculate Delta n_g first.
Temperature or reaction orientation is not defined
Needs reviewWhy it happens
Preparation Intelligence classification: Needs Review.
How it is corrected
Do not compare K values until both are fixed.
FAQ
Straight answers about how Rank Sarthi fits into serious exam preparation.
They have the same algebraic form for a given reaction, but Q uses the current composition while K describes equilibrium at a specified temperature.
No. It changes rates of approach to equilibrium, not the thermodynamic equilibrium constant.
In the standard ideal-gas textbook treatment, with Delta n counting gaseous stoichiometric coefficients.
Official scope is taken from the NEET (UG) 2026 syllabus and official NTA documents; concept structure follows current NCERT contents. No performance, weightage or question-frequency data is asserted.