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HKDSE Chemistry | Chemical equilibrium and Le Chatelier teaching guide | Kc = 64, 80% conversion, 15% Haber yield

HKDSE Chemistry | Chemical equilibrium and Le Chatelier teaching guide | Kc = 64, 80% conversion, 15% Haber yield

  • 2026-11-03

Students can recite that rates become equal at equilibrium, then plug the initial moles straight into Kc. One set of numbers, 0.50 and 0.50 going to 0.80, takes the class from the definition to Kc = 64 and then back to why industry accepts a 15% yield.

Objectives — Students can: (1) explain that equilibrium is dynamic, with equal forward and reverse rates rather than a stopped reaction; (2) build an ICE table and calculate Kc = 64 from the equilibrium concentrations; (3) predict the shift under concentration, pressure and temperature changes, and explain why the Haber process runs at only about 15% conversion per pass.

01 Prerequisites (3-minute check)

If any of these fails, fix it before the lesson starts.

Skill Quick check Pass mark
Reversible reactions What does the symbol mean? Both directions proceed at once
Molar concentration How is concentration calculated? Moles divided by volume in dm3
Exothermic reactions What does a negative enthalpy change mean? Energy is released

02 Lesson flow (60 minutes)

Time Stage Tutor does Student does
0-8 min What equilibrium is Dynamic, equal rates, constant concentrations Stress that it never stops
8-20 min ICE table Initial, change, equilibrium rows Change row follows coefficients
20-32 min Kc calculation Substitute equilibrium values to get 64 Never use initial values
32-42 min Le Chatelier Concentration, pressure, temperature No shift when gas moles are equal
42-52 min Haber trade-off Low temperature and high pressure help yield, not rate Catalysts do not change Kc
52-60 min Exit check Three questions in class Every student states 80%

03 Teaching script (read it out)

Scene 1: Act 1: equilibrium is dynamic, not stopped

Ask the class what equilibrium means. Most will say the reaction has stopped. Correct that first: both directions still run, but at equal rates, so the concentrations stop changing.
Use a door analogy: ten people enter and ten leave every minute, so the number inside is constant while people keep moving.
Then give the exam wording: forward and reverse rates are equal but not zero, the system is closed, temperature is fixed, and macroscopic properties such as colour, pressure and concentration stay steady.

Blackboard line: equal rates, constant concentrations.

Scene 2: Act 2: ICE tables and Kc, one line at a time

Write H2(g) + I2(g) ⇌ 2HI(g) with 0.50 mol dm-3 of each starting material and 0.80 mol dm-3 of HI at equilibrium.
The change row follows the coefficients: HI goes from 0 to 0.80, so 0.80 is formed and each reactant loses 0.40, leaving 0.10 of each.
Kc = [HI]2 / ([H2][I2]) = 0.64 / 0.01 = 64.
Conversion = 0.40 / 0.50 x 100% = 80%. Note that Kc happens to be unitless here; in general it carries units.

Make them compute Kc = 64 from 0.80 themselves.

Scene 3: Act 3: Le Chatelier and the industrial trade-off

Le Chatelier in one line: a system shifts to oppose the disturbance.
Adding a reactant or removing a product shifts right. Increasing pressure shifts towards the side with fewer gas moles; here both sides have 2, so there is no shift, which is the most common error. Raising temperature shifts towards the endothermic direction; this forward reaction is exothermic, so Kc falls and the mixture shifts left.
Haber process: N2 + 3H2 ⇌ 2NH3, enthalpy change -92 kJ mol-1. Low temperature favours yield but is far too slow, so plants use about 450 C, 200 atm and an iron catalyst, achieving roughly 15% per pass with unreacted gas recycled. A catalyst speeds up reaching equilibrium only; it changes neither Kc nor the final yield.

Remember: equal gas moles means pressure does not shift it.

04 Question types and worked steps

Type Example Steps Answer
ICE table Find Kc from initial and equilibrium data Three rows, convert by coefficients, use equilibrium values 0.64 / 0.01 = 64
Direction of shift Effect of increasing pressure Count gas moles on both sides first Two against two, so no shift
Temperature effect How Kc changes on heating Decide whether the forward reaction is exothermic Exothermic, so Kc decreases
Industrial question Why not run the Haber process colder Trade yield against rate Too slow, so 450 C is used
Sanity check (teach this): Kc uses equilibrium values only; substituting 0.50 gives 2.56, not 64.
Count gas moles before predicting a pressure effect: when the change is zero there is no shift, only a faster approach.
A catalyst changes neither Kc nor the yield.
Conversion is amount reacted over amount started: 0.40 / 0.50 = 80%.

05 Independent practice (3 questions)

Question Answer What to watch
Value of Kc 64 0.64 divided by 0.01
Conversion of H2 80% 0.40 divided by 0.50
Moles of HI at equilibrium in 1 dm3 0.80 mol Concentration times volume
Doubling pressure: relation between Q and Kc Q equals Kc, no shift Numerator and denominator both times four

06 Common mistakes and what to say

Mistake Student writes Say this
Using initial concentrations in Kc Answering 2.56 “Kc only reads the equilibrium row; the initial row is history.”
Assuming pressure always shifts right Answering that pressure shifts to products “Count the gas molecules first: two against two means no shift.”
Treating a catalyst as raising yield Answering that the catalyst shifts equilibrium “A catalyst gets you there faster, it does not move the destination.”
Calculating conversion from product Answering 160% “Conversion measures reactant used up, not product formed.”

07 Homework (paper, section and question numbers)

08 Exit check (last 5 minutes)

Question Answer Decision
Value of Kc 64 Wrong means redo the ICE table
Effect of pressure when gas moles are equal No shift, only faster Wrong means repeat act three
Haber conversion per pass About 15% Cannot answer means revisit the trade-off

09 Tutor FAQ

Does the reaction really stop at equilibrium?

No. Both directions continue at equal rates, which is why concentrations stay constant.

Does Kc change with concentration?

No. Kc depends on temperature only; a concentration change moves Q away from Kc and the system shifts back.

Why does a catalyst not change the yield?

It speeds up both directions equally, so equilibrium arrives sooner at the same position.

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