Chemistry • Year 11 • Module 2 • Lesson 3
Empirical and Molecular Formulas
Apply the four-step method and percentage composition calculations to worked scenarios, data tables, and real-compound contexts.
1. Complete the worked solution — aspirin
Aspirin (acetylsalicylic acid) contains 60.00% carbon, 4.44% hydrogen, and 35.56% oxygen by mass. Its molar mass is 180.16 g mol−1. The table below shows Steps 1–2 of the four-step method already completed. Complete Steps 3 and 4. (C = 12.011, H = 1.008, O = 15.999) 8 marks
| Step | C | H | O |
|---|---|---|---|
| Step 1 — Assume 100 g: % → g | 60.00 g | 4.44 g | 35.56 g |
| Step 2 — Convert to moles (n = m ÷ MM) | 60.00 ÷ 12.011 = 4.996 mol | 4.44 ÷ 1.008 = 4.405 mol | 35.56 ÷ 15.999 = 2.223 mol |
| Step 3 — Divide by smallest (2.223); round to whole numbers | |||
| Empirical formula | |||
| Step 4 — MM(empirical formula) = ? | |||
| Multiplier n = MM(molecular) ÷ MM(empirical) | |||
| Molecular formula | |||
2. Classify and complete — five compounds
The table below lists five compounds with their molecular formulas. Complete the empirical formula column, then tick whether the empirical and molecular formulas are the same or different. 10 marks (1 EF + 1 same/different each)
| Compound | Molecular formula | Empirical formula | Same as MF? |
|---|---|---|---|
| Water | H2O | ||
| Hydrogen peroxide | H2O2 | ||
| Benzene | C6H6 | ||
| Butane | C4H10 | ||
| Phosphorus pentoxide | P4O10 |
2.1 For which of the five compounds above is the empirical formula identical to the molecular formula? Explain, in one sentence, what this tells you about the multiplier n for those compounds. 2 marks
3. Calculate percentage composition — ammonium nitrate
Ammonium nitrate, NH4NO3, is used as a fertiliser in Australian agriculture. Calculate the percentage by mass of each element. Show full working, including the molar mass calculation. Check that your percentages sum to 100 %. (N = 14.007, H = 1.008, O = 15.999) 5 marks
3.1 MM(NH4NO3) =
3.2 % N =
3.3 % H =
3.4 % O =
3.5 Check: = 100% ✓
4. Find the missing element — ethanol combustion scenario
A student performs combustion analysis on an unknown organic compound. The results show 52.17% carbon and 13.04% hydrogen by mass. The percentage of the remaining element is not directly stated. 7 marks
4.1 Calculate the percentage of the unknown element and identify which element it most likely is. 2 marks
4.2 Use the four-step method to determine the empirical formula of the compound. Show all working. (C = 12.011, H = 1.008, O = 15.999) 4 marks
4.3 The compound’s molar mass is 46.07 g mol−1. Calculate the multiplier n and state the molecular formula. 1 mark
5. Contrast two compounds with the same empirical formula
Glucose (C6H12O6, molar mass 180.16 g mol−1) and fructose (C6H12O6, molar mass 180.16 g mol−1) are both found in Australian honey. 5 marks
5.1 State the empirical formula shared by glucose and fructose. Show that MM(empirical) and the multiplier n are the same for both compounds. 3 marks
5.2 The lesson states that glucose and fructose are “completely different substances” despite sharing the same molecular formula. Using only what this lesson teaches about empirical and molecular formulas, explain what this tells us about the completeness of the molecular formula as a description of a compound. 2 marks
Q1 — Aspirin worked solution
Step 3 — Divide by smallest (2.223):
C: 4.996 ÷ 2.223 = 2.248 • H: 4.405 ÷ 2.223 = 1.981 ≈ 2 • O: 2.223 ÷ 2.223 = 1.000
The ratio C : H : O = 2.248 : 2 : 1. Since 2.248 is not close to a whole number, multiply all values by 4: C = 8.99 ≈ 9, H = 7.92 ≈ 8, O = 4.00 = 4. All are now whole numbers.
Empirical formula: C9H8O4
Step 4: MM(C9H8O4) = 9(12.011) + 8(1.008) + 4(15.999) = 108.099 + 8.064 + 63.996 = 180.159 g mol−1.
n = 180.16 ÷ 180.159 ≈ 1. The molecular formula is the same as the empirical formula: Molecular formula = C9H8O4.
Marking note: Award marks for consistent application of the 4-step method. The key insight is recognising that 2.248 requires multiplication by 4 (not rounding to 2) to give whole-number subscripts. Accept C9H8O4 for both empirical and molecular formula.
Q2 — Five compounds table
Water H2O → EF = H2O, Same. • Hydrogen peroxide H2O2 → EF = HO, Different. • Benzene C6H6 → EF = CH, Different. • Butane C4H10 → EF = C2H5, Different. • Phosphorus pentoxide P4O10 → EF = P2O5, Different.
Q2.1: Only water has the same empirical and molecular formula [1]. This tells us that the multiplier n = 1 for water — the empirical formula is already the simplest possible representation of the actual molecule [1].
Q3 — Ammonium nitrate % composition
MM(NH4NO3) = 2(14.007) + 4(1.008) + 3(15.999) = 28.014 + 4.032 + 47.997 = 80.043 g mol−1 [1]
% N = 28.014 ÷ 80.043 × 100 = 35.00% [1]
% H = 4.032 ÷ 80.043 × 100 = 5.04% [1]
% O = 47.997 ÷ 80.043 × 100 = 59.96% [1]
Check: 35.00 + 5.04 + 59.96 = 100.00% ✓ [1]
Q4 — Ethanol combustion scenario
4.1: % unknown = 100 − 52.17 − 13.04 = 34.78%. For an organic compound (containing C and H), the third element is most likely oxygen [1 for calculation + 1 for identification].
4.2 (four-step method):
Step 1: C = 52.17 g, H = 13.04 g, O = 34.78 g [1]
Step 2: n(C) = 52.17 ÷ 12.011 = 4.344; n(H) = 13.04 ÷ 1.008 = 12.937; n(O) = 34.78 ÷ 15.999 = 2.174 [1]
Step 3: Divide by 2.174: C = 1.998 ≈ 2; H = 5.951 ≈ 6; O = 1.000 [1]. Empirical formula = C2H6O [1]
4.3: MM(C2H6O) = 2(12.011) + 6(1.008) + 15.999 = 24.022 + 6.048 + 15.999 = 46.069 g mol−1. n = 46.07 ÷ 46.069 = 1.00 ≈ 1. Molecular formula = C2H6O (ethanol) [1].
Q5 — Glucose and fructose
5.1: C6H12O6 → divide all subscripts by 6 (HCF) → empirical formula = CH2O [1]. MM(CH2O) = 12.011 + 2(1.008) + 15.999 = 30.026 g mol−1. n = 180.16 ÷ 30.026 = 5.999 ≈ 6 for both glucose and fructose [1 for MM calculation + 1 for n].
5.2: The molecular formula identifies the number and type of atoms in a molecule, but does not uniquely identify a compound [1]. Glucose and fructose both have the molecular formula C6H12O6 yet are completely different substances with different properties — this shows that knowing the molecular formula alone is not sufficient to identify a compound; additional information about the compound (such as physical properties or other experimental data) is needed [1].