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Chemistry · Ch 6 — Equilibrium

Factors Affecting Equilibria

6.8

Factors Affecting Equilibria

6.8 Factors Affecting Equilibria

The central goal in chemical synthesis is to get the maximum possible conversion of reactants into products while using the least energy. That means achieving a high yield under mild conditions of temperature and pressure. When a reaction does not give a satisfactory yield, the experimental conditions must be adjusted. The Haber process for ammonia synthesis — producing roughly a hundred million tonnes of ammonia each year, mostly for fertilisers — is a classic example where the choice of conditions has enormous economic importance.

The equilibrium constant KcK_c is independent of initial concentrations. But if a system at equilibrium is disturbed — by changing the concentration of a reactant or product, or by altering temperature or pressure — the system is no longer at equilibrium. A net reaction then proceeds in one direction until equilibrium is re-established.

To predict which direction the reaction will shift, we use Le Chatelier's principle.

Important

Le Chatelier's principle: If a change is made to any of the factors that determine the equilibrium conditions of a system, the system will shift in such a way as to reduce or counteract the effect of that change.

This principle applies to all physical and chemical equilibria. We now examine each factor that can influence equilibrium.

The Four Factors, Section by Section

Each factor gets its own detailed treatment: concentration changes (§6.8.1), pressure changes (§6.8.2), inert-gas addition (§6.8.3), temperature changes (§6.8.4) and the role of a catalyst (§6.8.5).

Note

Beyond the textbook — the van't Hoff equation. The NCERT text treats the effect of temperature qualitatively; the quantitative relationship (useful in competitive exams) is the van't Hoff equation,

ln⁡K2K1=−ΔH∘R(1T2−1T1)\ln\frac{K_2}{K_1} = -\frac{\Delta H^\circ}{R}\left(\frac{1}{T_2} - \frac{1}{T_1}\right)

For an exothermic reaction (ΔH∘<0\Delta H^\circ < 0), KK decreases as temperature rises; for an endothermic reaction it increases.

Summary Table of Effects

Change appliedDirection of shiftEffect on KK
Increase concentration of reactantForward (right)No change