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14.10:

The Small x Assumption

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Chemistry
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The Small x Assumption

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The small x assumption is an approximation that can be used under certain conditions to simplify solving the equilibrium expression and to avoid using the quadratic formula. 

If the equilibrium constant for a reaction is small and the initial concentrations of reactants are sufficiently high, it is possible that only a small amount of reactants will be converted into products.

When these conditions are met, the equilibrium concentrations can be approximated using the assumption that the change in the initial concentrations is negligible. However, it must be confirmed that the change in concentration, x, is less than 5% of the initial concentrations to show the the assumption was valid.

The decomposition of 0.66 molar carbonyl dichloride gas produces carbon monoxide and chlorine gas, and the equilibrium constant for this reaction is 2.2 × 10−10.

To calculate the equilibrium concentrations, the values are tabulated in the ICE table along with the change and equilibrium concentrations.

Substituting the equilibrium concentrations in the expression, K equals x squared divided by 0.66 minus x. As K is very small, the change in the initial concentration, x, of carbonyl dichloride is expected to be negligible.

Therefore, 0.66 minus x can be approximated to 0.66. When solved, x equals 1.2 × 10−5 molar.

Here, x is only 0.0018 percent of the initial 0.66 molar concentration of carbonyl dichloride, which is far less than the 5% maximum allowed. Thus, the small x assumption is valid here.

Using the value for x in the ICE table, the equilibrium concentration of carbonyl dichloride is still 0.66 molar with significant figures, while the concentrations of carbon monoxide and chlorine are both 1.2 × 10−5 molar.

14.10:

The Small x Assumption

If a reaction has a small equilibrium constant, the equilibrium position favors the reactants. In such reactions, a negligible change in concentration may occur if the initial concentrations of reactants are high and the Kc value is small. In such circumstances, the equilibrium concentration is approximately equal to its initial concentration.  This estimation can be used to simplify the equilibrium calculations by assuming that some equilibrium concentrations are equal to the initial concentrations. However, to make this assumption, the change in the concentration of a weak acid or base, i.e., x, must be less than 5% of its initial concentration. If x is more than 5%, then the quadratic formula needs to be used to solve the equilibrium equation.  

Calculation of Equilibrium Concentrations Using an Algebra-Simplifying Assumption

What are the concentrations at equilibrium of a 0.15 M solution of HCN?

Eq1

Using x to represent the concentration of each product at equilibrium gives this ICE table.

 HCN (aq)           H+ (aq) CN(aq)
Initial Concentration (M) 0.15 0 0
Change (M) −x +x +x
Equilibrium Concentration (M) 0.15 − x x x

Substitute the equilibrium concentration terms into the Kc expression

Eq2

rearrange to the quadratic form and solve for x

Eq3

Thus, [H+] = [CN] = x = 8.6 × 10–6 M and [HCN] = 0.15 – x = 0.15 M.

Note in this case that the change in concentration is significantly less than the initial concentration (a consequence of the small K), and so the initial concentration experiences a negligible change:

Eq4

This approximation allows for a more expedient mathematical approach to the calculation that avoids the need to solve for the roots of a quadratic equation:

Eq5

The value of x calculated is, indeed, much less than the initial concentration

Eq6

and so the approximation was justified. If this simplified approach were to yield a value for x that did not justify the approximation, the calculation would need to be repeated without making the approximation.

This text has been adapted from Openstax, Chemistry 2e, Section 13.4 Equilibrium Calculations.

Suggested Reading

  1. Lim, Kieran F. "Using graphics calculators and spreadsheets in chemistry: Solving equilibrium problems." Journal of Chemical Education 85, no. 10 (2008): 1347. https://pubs.acs.org/doi/pdf/10.1021/ed085p1347