Reacting Masses, Yield and Limiting Reagents

AS · 9 min

A balanced equation is a recipe written in moles. Once you can turn masses into moles and back, you can predict how much product a reaction should give, work out which reactant runs out first, compare the actual yield with the theoretical one, and even deduce an unknown equation from experimental masses. These calculations appear in every Paper 2 and in Paper 3 data analysis, usually as a multi-step question where each step carries a mark.

The mole ratio is the bridge

The coefficients in a balanced equation give the ratio of amounts in moles, not masses. In

2 Mg(s)+OX2(g)→2 MgO(s)\ce{2Mg(s) + O2(g) -> 2MgO(s)}

two moles of magnesium react with one mole of oxygen molecules to make two moles of magnesium oxide. The masses are in the ratio 48.6:32.0:80.648.6 : 32.0 : 80.6, which is not 2:1:22 : 1 : 2.

Method

Reacting-mass calculation

  1. Write the balanced equation.
  2. Convert the known mass to moles: n=m/Mn = m / M.
  3. Use the mole ratio from the equation to find moles of the substance you want.
  4. Convert back to mass: m=n×Mm = n \times M.
  5. Round the final answer sensibly (normally to the same number of significant figures as the data, usually 3).
Mass of product from a thermal decomposition

Calculate the mass of calcium oxide formed when 25.0 g25.0\ \text{g} of calcium carbonate is heated until it has completely decomposed.

SolutionCaCOX3(s)→CaO(s)+COX2(g)\ce{CaCO3(s) -> CaO(s) + CO2(g)}

n(CaCOX3)=25.0100.1=0.2498 moln(\ce{CaCO3}) = \dfrac{25.0}{100.1} = 0.2498\ \text{mol}

Mole ratio CaCOX3:CaO=1:1\ce{CaCO3} : \ce{CaO} = 1 : 1, so n(CaO)=0.2498 moln(\ce{CaO}) = 0.2498\ \text{mol}.

m(CaO)=0.2498×56.1=14.0 gm(\ce{CaO}) = 0.2498 \times 56.1 = 14.0\ \text{g}

Percentage yield

The mass calculated from the equation is the theoretical yield: the maximum mass of product if every particle of the limiting reactant reacts as the equation says. In practice the actual yield is less, because:

  • the reaction may be reversible and not go to completion;
  • side reactions make other products;
  • product is lost during transfer, filtration, distillation or purification;
  • some reactant may be impure.
Key result
percentage yield=actual yieldtheoretical yield×100\text{percentage yield} = \frac{\text{actual yield}}{\text{theoretical yield}} \times 100

Both yields must be in the same units (both masses or both amounts in moles).

Percentage yield of an ester

6.00 g6.00\ \text{g} of ethanoic acid is heated with excess ethanol and a little concentrated sulfuric acid. 6.16 g6.16\ \text{g} of ethyl ethanoate is collected. Calculate the percentage yield.

CHX3COOH+CX2HX5OH⇌CHX3COOCX2HX5+HX2O\ce{CH3COOH + C2H5OH <=> CH3COOC2H5 + H2O}
Solution

n(CHX3COOH)=6.0060.0=0.100 moln(\ce{CH3COOH}) = \dfrac{6.00}{60.0} = 0.100\ \text{mol}

Mole ratio 1:11 : 1, so the theoretical n(ester)=0.100 moln(\text{ester}) = 0.100\ \text{mol}.

Theoretical mass =0.100×88.0=8.80 g= 0.100 \times 88.0 = 8.80\ \text{g}.

percentage yield=6.168.80×100=70.0%\text{percentage yield} = \frac{6.16}{8.80} \times 100 = 70.0\%

A large part of the shortfall here is because esterification is reversible and reaches equilibrium.

Limiting and excess reagents

Reactants are often not mixed in the exact ratio of the equation. The reactant that is used up first is the limiting reagent; it decides how much product forms. The other reactant is in excess, and some of it is left over.

Method

Finding the limiting reagent

  1. Calculate the moles of each reactant.
  2. Divide each by its coefficient in the equation. The smallest result identifies the limiting reagent.
  3. Use the moles of the limiting reagent, with the mole ratio, to find the product.
  4. To find the excess left: moles of excess reagent present minus moles that react.
Iron and sulfur

5.58 g5.58\ \text{g} of iron is heated with 4.00 g4.00\ \text{g} of sulfur: Fe(s)+S(s)→FeS(s)\ce{Fe(s) + S(s) -> FeS(s)}. Identify the limiting reagent and calculate the mass of iron(II) sulfide formed and the mass of the reactant left over.

Solution

n(Fe)=5.5855.8=0.100 moln(\ce{Fe}) = \dfrac{5.58}{55.8} = 0.100\ \text{mol}; n(S)=4.0032.1=0.1246 moln(\ce{S}) = \dfrac{4.00}{32.1} = 0.1246\ \text{mol}.

The ratio is 1:11 : 1, and there is less iron, so iron is limiting.

n(FeS)=0.100 moln(\ce{FeS}) = 0.100\ \text{mol}; m=0.100×(55.8+32.1)=0.100×87.9=8.79 gm = 0.100 \times (55.8 + 32.1) = 0.100 \times 87.9 = 8.79\ \text{g}.

Sulfur left =0.1246−0.100=0.0246 mol= 0.1246 - 0.100 = 0.0246\ \text{mol}, mass =0.0246×32.1=0.790 g= 0.0246 \times 32.1 = 0.790\ \text{g}.

A limiting reagent when the ratio is not 1 : 1

2.70 g2.70\ \text{g} of aluminium reacts with 7.10 g7.10\ \text{g} of chlorine: 2 Al(s)+3 ClX2(g)→2 AlClX3(s)\ce{2Al(s) + 3Cl2(g) -> 2AlCl3(s)}. Find the mass of aluminium chloride formed.

Solution

n(Al)=2.7027.0=0.100 moln(\ce{Al}) = \dfrac{2.70}{27.0} = 0.100\ \text{mol}; n(ClX2)=7.1071.0=0.100 moln(\ce{Cl2}) = \dfrac{7.10}{71.0} = 0.100\ \text{mol}.

Divide by coefficients: Al\ce{Al}: 0.100/2=0.05000.100 / 2 = 0.0500; ClX2\ce{Cl2}: 0.100/3=0.03330.100 / 3 = 0.0333. Chlorine gives the smaller value, so chlorine is limiting (0.100 mol of Al would need 0.150 mol of ClX2\ce{Cl2}).

n(AlClX3)=0.100×23=0.0667 moln(\ce{AlCl3}) = 0.100 \times \tfrac{2}{3} = 0.0667\ \text{mol}; m=0.0667×133.5=8.90 gm = 0.0667 \times 133.5 = 8.90\ \text{g}.

Watch out

Equal numbers of moles do not mean neither is limiting. Always compare against the equation's ratio. In the aluminium example, 0.100 mol of each looks balanced, but the equation needs 1.5 times as much chlorine as aluminium.

Deducing an equation from reacting masses

Experimental masses can reveal the stoichiometry of a reaction you have not seen before. Convert every mass to moles and find the simplest whole-number ratio.

Exam-style: deducing the formula of a chloride

1.12 g1.12\ \text{g} of iron reacts completely with chlorine to form 3.25 g3.25\ \text{g} of an iron chloride. Deduce the formula of the chloride and write an equation for its formation.

Solution

Mass of chlorine combined =3.25−1.12=2.13 g= 3.25 - 1.12 = 2.13\ \text{g}.

n(Fe)=1.1255.8=0.02007 moln(\ce{Fe}) = \dfrac{1.12}{55.8} = 0.02007\ \text{mol}; n(Cl)=2.1335.5=0.0600 moln(\ce{Cl}) = \dfrac{2.13}{35.5} = 0.0600\ \text{mol}.

Ratio Fe:Cl=0.02007:0.0600=1:2.99≈1:3\ce{Fe} : \ce{Cl} = 0.02007 : 0.0600 = 1 : 2.99 \approx 1 : 3. The chloride is FeClX3\ce{FeCl3}, iron(III) chloride.

2 Fe(s)+3 ClX2(g)→2 FeClX3(s)\ce{2Fe(s) + 3Cl2(g) -> 2FeCl3(s)}
Exam-hard: composition of a mixture from mass loss

A 10.00 g10.00\ \text{g} mixture of sodium hydrogencarbonate and sodium chloride is heated to constant mass. The mass decreases by 2.17 g2.17\ \text{g}. Sodium chloride does not decompose. Calculate the percentage by mass of sodium hydrogencarbonate in the mixture.

2 NaHCOX3(s)→NaX2COX3(s)+COX2(g)+HX2O(g)\ce{2NaHCO3(s) -> Na2CO3(s) + CO2(g) + H2O(g)}
Solution

The mass lost is the carbon dioxide and water that escape. For every 2 mol of NaHCOX3\ce{NaHCO3}, 1 mol of COX2\ce{CO2} (44.0 g) and 1 mol of HX2O\ce{H2O} (18.0 g) are lost: 62.0 g62.0\ \text{g} per 2 mol of NaHCOX3\ce{NaHCO3}.

n(NaHCOX3)=2×2.1762.0=0.0700 moln(\ce{NaHCO3}) = 2 \times \frac{2.17}{62.0} = 0.0700\ \text{mol}

m(NaHCOX3)=0.0700×84.0=5.88 gm(\ce{NaHCO3}) = 0.0700 \times 84.0 = 5.88\ \text{g}

percentage=5.8810.00×100=58.8%\text{percentage} = \frac{5.88}{10.00} \times 100 = 58.8\%

Significant figures in calculations

Cambridge expects answers to reflect the precision of the data.

  • Give the final answer to the same number of significant figures as the least precise data value, unless the question says otherwise. With data to 3 s.f., give 3 s.f.
  • Never round an intermediate value to fewer figures than the final answer needs. Carry at least one extra figure, or keep the full value in your calculator.
  • Do not "lose" significant figures: 14.0 g14.0\ \text{g} is 3 s.f., but 14 g14\ \text{g} is only 2.
Exam tip
  • Show every step: equation, moles of the known, ratio, moles of the unknown, mass. Method marks are awarded for each, so a slip in arithmetic costs one mark, not all of them.
  • Label each quantity: "n(CaCOX3)=…n(\ce{CaCO3}) = \ldots". It helps the examiner follow you and stops you dividing by the wrong molar mass.
  • In limiting reagent questions, state explicitly which reagent is limiting and why.
  • A percentage yield over 100% means a mistake (or an impure, wet product in a practical question).
Summary
  • Equations give mole ratios, not mass ratios.
  • Method: mass to moles, use the ratio, moles to mass.
  • Percentage yield =actualtheoretical×100= \dfrac{\text{actual}}{\text{theoretical}} \times 100. Yields are below 100% because of incomplete or reversible reactions, side reactions and losses.
  • The limiting reagent has the smallest value of moles divided by its coefficient; it fixes the amount of product.
  • Experimental masses can be turned into a mole ratio to deduce a formula or an equation.
  • Keep extra figures during working; round at the end to the precision of the data.

Practice

Question
  1. Calculate the mass of iron that could be extracted from 1.00 kg1.00\ \text{kg} of iron(III) oxide: FeX2OX3+3 CO→2 Fe+3 COX2\ce{Fe2O3 + 3CO -> 2Fe + 3CO2}.
  2. Calculate the mass of oxygen needed to burn 11.6 g11.6\ \text{g} of butane completely: 2 CX4HX10+13 OX2→8 COX2+10 HX2O\ce{2C4H10 + 13O2 -> 8CO2 + 10H2O}.
  3. 12.0 g12.0\ \text{g} of magnesium is burnt and 18.0 g18.0\ \text{g} of magnesium oxide is collected. Calculate the percentage yield.
  4. 10.0 g10.0\ \text{g} of hydrogen reacts with 40.0 g40.0\ \text{g} of oxygen to form water. Identify the limiting reagent, the mass of water formed, and the mass of the excess reagent left.
  5. 2.00 g2.00\ \text{g} of a copper oxide is reduced by hydrogen to 1.60 g1.60\ \text{g} of copper. Deduce the formula of the oxide.
  6. Dehydration of 9.20 g9.20\ \text{g} of ethanol gives 3.92 g3.92\ \text{g} of ethene: CX2HX5OH→CX2HX4+HX2O\ce{C2H5OH -> C2H4 + H2O}. Calculate the percentage yield.
  7. Propan-1-ol is oxidised to propanoic acid with a 75.0% yield. What mass of propan-1-ol is needed to produce 6.00 g6.00\ \text{g} of propanoic acid?
  8. Calculate the mass of magnesium oxide formed when 7.42 g7.42\ \text{g} of magnesium nitrate decomposes: 2 Mg(NOX3)X2→2 MgO+4 NOX2+OX2\ce{2Mg(NO3)2 -> 2MgO + 4NO2 + O2}.
  9. A 2.00 g2.00\ \text{g} mixture of calcium carbonate and magnesium carbonate is heated to constant mass, leaving 1.055 g1.055\ \text{g} of a mixture of CaO\ce{CaO} and MgO\ce{MgO}. Calculate the percentage by mass of calcium carbonate in the original mixture.
  10. 1.00 g1.00\ \text{g} of calcium reacts completely with a halogen, XX2\ce{X2}, to form 2.77 g2.77\ \text{g} of CaXX2\ce{CaX2}. Identify X.
Answers
  1. n(FeX2OX3)=1000/159.6=6.266 moln(\ce{Fe2O3}) = 1000 / 159.6 = 6.266\ \text{mol}; n(Fe)=2×6.266=12.53 moln(\ce{Fe}) = 2 \times 6.266 = 12.53\ \text{mol}; m=12.53×55.8=699 gm = 12.53 \times 55.8 = 699\ \text{g}.
  2. n(CX4HX10)=11.6/58.0=0.200 moln(\ce{C4H10}) = 11.6 / 58.0 = 0.200\ \text{mol}; n(OX2)=0.200×132=1.30 moln(\ce{O2}) = 0.200 \times \tfrac{13}{2} = 1.30\ \text{mol}; m=1.30×32.0=41.6 gm = 1.30 \times 32.0 = 41.6\ \text{g}.
  3. Theoretical: n(Mg)=12.0/24.3=0.4938 mol=n(MgO)n(\ce{Mg}) = 12.0 / 24.3 = 0.4938\ \text{mol} = n(\ce{MgO}); m=0.4938×40.3=19.9 gm = 0.4938 \times 40.3 = 19.9\ \text{g}. Yield =18.0/19.9×100=90.4%= 18.0 / 19.9 \times 100 = 90.4\%.
  4. 2 HX2+OX2→2 HX2O\ce{2H2 + O2 -> 2H2O}. n(HX2)=10.0/2.0=5.00n(\ce{H2}) = 10.0 / 2.0 = 5.00; n(OX2)=40.0/32.0=1.25n(\ce{O2}) = 40.0 / 32.0 = 1.25. Divide by coefficients: 2.502.50 and 1.251.25, so oxygen is limiting. n(HX2O)=2.50 moln(\ce{H2O}) = 2.50\ \text{mol}, m=45.0 gm = 45.0\ \text{g}. Hydrogen used =2.50 mol= 2.50\ \text{mol}; left =2.50 mol=5.0 g= 2.50\ \text{mol} = 5.0\ \text{g}.
  5. n(Cu)=1.60/63.5=0.0252n(\ce{Cu}) = 1.60 / 63.5 = 0.0252; n(O)=0.40/16.0=0.0250n(\ce{O}) = 0.40 / 16.0 = 0.0250. Ratio 1:11 : 1: CuO\ce{CuO}.
  6. n(CX2HX5OH)=9.20/46.0=0.200 moln(\ce{C2H5OH}) = 9.20 / 46.0 = 0.200\ \text{mol}; theoretical ethene =0.200×28.0=5.60 g= 0.200 \times 28.0 = 5.60\ \text{g}; yield =3.92/5.60×100=70.0%= 3.92 / 5.60 \times 100 = 70.0\%.
  7. n(acid)=6.00/74.0=0.08108 moln(\text{acid}) = 6.00 / 74.0 = 0.08108\ \text{mol}. With 75.0% yield, n(alcohol)=0.08108/0.750=0.1081 moln(\text{alcohol}) = 0.08108 / 0.750 = 0.1081\ \text{mol}; m=0.1081×60.0=6.49 gm = 0.1081 \times 60.0 = 6.49\ \text{g}.
  8. M(Mg(NOX3)X2)=148.3M(\ce{Mg(NO3)2}) = 148.3; n=7.42/148.3=0.05003 mol=n(MgO)n = 7.42 / 148.3 = 0.05003\ \text{mol} = n(\ce{MgO}); m=0.05003×40.3=2.02 gm = 0.05003 \times 40.3 = 2.02\ \text{g}.
  9. Let the mass of CaCOX3\ce{CaCO3} be xx g; MgCOX3\ce{MgCO3} is (2.00−x)(2.00 - x) g. Mass of CaO\ce{CaO} =x×56.1100.1=0.5604x= x \times \tfrac{56.1}{100.1} = 0.5604x; mass of MgO\ce{MgO} =(2.00−x)×40.384.3=0.4781(2.00−x)= (2.00 - x) \times \tfrac{40.3}{84.3} = 0.4781(2.00 - x). So 0.5604x+0.9561−0.4781x=1.0550.5604x + 0.9561 - 0.4781x = 1.055, giving 0.0824x=0.09890.0824x = 0.0989 and x=1.20 gx = 1.20\ \text{g}. Percentage =1.20/2.00×100=60.0%= 1.20 / 2.00 \times 100 = 60.0\%.
  10. n(Ca)=1.00/40.1=0.02494 mol=n(CaXX2)n(\ce{Ca}) = 1.00 / 40.1 = 0.02494\ \text{mol} = n(\ce{CaX2}). Mass of X =2.77−1.00=1.77 g= 2.77 - 1.00 = 1.77\ \text{g}, which is 2×0.02494=0.04988 mol2 \times 0.02494 = 0.04988\ \text{mol} of X atoms. Ar(X)=1.77/0.04988=35.5A_r(\ce{X}) = 1.77 / 0.04988 = 35.5: X is chlorine.

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