V m = n R T P = 1 × 0.0821 × 273 1 = 22.4 d m 3 V_m = \dfrac{nRT}{P} = \dfrac{1 \times 0.0821 \times 273}{1} = 22.4 \mathrm{ dm}^3 V m = P n R T = 1 1 × 0.0821 × 273 = 22.4 dm 3
This confirms the molar volume at STP.
Worked example 12: Calculate the volume occupied by 5.00 g of O 2 \mathrm{O}_2 O 2 at 2.0 atm and 27 ∘ C 27^\circ\mathrm{C} 2 7 ∘ C .
Answer n = 5.00 / 32.0 = 0.156 m o l n = 5.00 / 32.0 = 0.156 \mathrm{ mol} n = 5.00/32.0 = 0.156 mol
T = 27 + 273 = 300 K T = 27 + 273 = 300 \mathrm{ K} T = 27 + 273 = 300 K
V = n R T P = 0.156 × 0.0821 × 300 2.0 = 3.842 2.0 = 1.92 d m 3 V = \dfrac{nRT}{P} = \dfrac{0.156 \times 0.0821 \times 300}{2.0} = \dfrac{3.842}{2.0} = 1.92 \mathrm{ dm}^3 V = P n R T = 2.0 0.156 × 0.0821 × 300 = 2.0 3.842 = 1.92 dm 3
The “mole triangle” connects n n n , m m m And M M M :
n = m M ; m = n × M ; M = m n n = \frac{m}{M} \quad ; \quad m = n \times M \quad ; \quad M = \frac{m}{n} n = M m ; m = n × M ; M = n m
For gases, also connect n n n , V V V And V m V_m V m :
n = V V m ; V = n × V m n = \frac{V}{V_m} \quad ; \quad V = n \times V_m n = V m V ; V = n × V m
Worked example 13: What volume of C O 2 \mathrm{CO}_2 CO 2 at RTP is produced when 25.0 g of C a C O 3 \mathrm{CaCO}_3 CaCO 3 reacts with excess HCl?
C a C O 3 + 2 H C l → C a C l 2 + H 2 O + C O 2 \mathrm{CaCO}_3 + 2\mathrm{HCl} \to \mathrm{CaCl}_2 + \mathrm{H}_2\mathrm{O} + \mathrm{CO}_2 CaCO 3 + 2 HCl → CaCl 2 + H 2 O + CO 2
Answer Moles of C a C O 3 = 25.0 / 100.1 = 0.250 m o l \mathrm{CaCO}_3 = 25.0 / 100.1 = 0.250 \mathrm{ mol} CaCO 3 = 25.0/100.1 = 0.250 mol
1 mol C a C O 3 \mathrm{CaCO}_3 CaCO 3 produces 1 mol C O 2 \mathrm{CO}_2 CO 2 So moles of C O 2 = 0.250 m o l \mathrm{CO}_2 = 0.250 \mathrm{ mol} CO 2 = 0.250 mol
Volume at RTP = 0.250 × 24.0 = 6.00 d m 3 0.250 \times 24.0 = 6.00 \mathrm{ dm}^3 0.250 × 24.0 = 6.00 dm 3
Volumetric analysis is a quantitative technique for determining the concentration of a solution by Reaction with a standard solution of known concentration.
Apparatus Purpose Burette Delivers variable volumes, graduated to 0.05 cm3 ^3 3 Pipette Delivers a fixed volume accurately Volumetric flask Prepares solutions of precise concentration Conical flask Contains the analyte for titration
General approach:
Write the balanced equation. Calculate moles of the standard solution used (n = c × V n = c \times V n = c × V ). Use the mole ratio to find moles of the unknown. Calculate concentration or mass of the unknown. Worked example 14: 25.0 cm3 ^3 3 of N a O H \mathrm{NaOH} NaOH solution is titrated against 0.100 mol/dm3 ^3 3 H C l \mathrm{HCl} HCl . The average titre is 20.0 cm3 ^3 3 . Calculate the concentration of N a O H \mathrm{NaOH} NaOH .
N a O H + H C l → N a C l + H 2 O \mathrm{NaOH} + \mathrm{HCl} \to \mathrm{NaCl} + \mathrm{H}_2\mathrm{O} NaOH + HCl → NaCl + H 2 O
Answer Moles of H C l = 0.100 × 20.0 / 1000 = 0.00200 m o l \mathrm{HCl} = 0.100 \times 20.0 / 1000 = 0.00200 \mathrm{ mol} HCl = 0.100 × 20.0/1000 = 0.00200 mol
Mole ratio N a O H : H C l = 1 : 1 \mathrm{NaOH}:\mathrm{HCl} = 1:1 NaOH : HCl = 1 : 1 So moles of N a O H = 0.00200 m o l \mathrm{NaOH} = 0.00200 \mathrm{ mol} NaOH = 0.00200 mol
c ( N a O H ) = 0.00200 25.0 / 1000 = 0.00200 0.0250 = 0.0800 m o l / d m 3 c(\mathrm{NaOH}) = \dfrac{0.00200}{25.0 / 1000} = \dfrac{0.00200}{0.0250} = 0.0800 \mathrm{ mol/dm}^3 c ( NaOH ) = 25.0/1000 0.00200 = 0.0250 0.00200 = 0.0800 mol/dm 3
Worked example 15: 1.00 g of impure N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 is dissolved in water and made Up to 250 cm3 ^3 3 . 25.0 cm3 ^3 3 of this solution requires 21.5 cm3 ^3 3 of 0.100 mol/dm3 ^3 3 H C l \mathrm{HCl} HCl for complete reaction. Calculate the percentage purity of the N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 .
N a 2 C O 3 + 2 H C l → 2 N a C l + H 2 O + C O 2 \mathrm{Na}_2\mathrm{CO}_3 + 2\mathrm{HCl} \to 2\mathrm{NaCl} + \mathrm{H}_2\mathrm{O} + \mathrm{CO}_2 Na 2 CO 3 + 2 HCl → 2 NaCl + H 2 O + CO 2
Answer Moles of H C l \mathrm{HCl} HCl used = 0.100 × 21.5 / 1000 = 0.00215 m o l 0.100 \times 21.5 / 1000 = 0.00215 \mathrm{ mol} 0.100 × 21.5/1000 = 0.00215 mol
Moles of N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 in 25.0 cm3 ^3 3 = 0.00215 / 2 = 0.001075 m o l 0.00215 / 2 = 0.001075 \mathrm{ mol} 0.00215/2 = 0.001075 mol
Moles of N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 in 250 cm3 ^3 3 = 0.001075 × 10 = 0.01075 m o l 0.001075 \times 10 = 0.01075 \mathrm{ mol} 0.001075 × 10 = 0.01075 mol
Mass of pure N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 = 0.01075 × 106.0 = 1.140 g 0.01075 \times 106.0 = 1.140 \mathrm{ g} 0.01075 × 106.0 = 1.140 g
Wait — this exceeds 1.00 g. Let me recalculate with correct titre.
Actually, let me use a more reasonable titre of 18.9 cm3 ^3 3 :
Moles of H C l \mathrm{HCl} HCl used = 0.100 × 18.9 / 1000 = 0.00189 m o l 0.100 \times 18.9 / 1000 = 0.00189 \mathrm{ mol} 0.100 × 18.9/1000 = 0.00189 mol
Moles of N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 in 25.0 cm3 ^3 3 = 0.00189 / 2 = 0.000945 m o l 0.00189 / 2 = 0.000945 \mathrm{ mol} 0.00189/2 = 0.000945 mol
Moles of N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 in 250 cm3 ^3 3 = 0.000945 × 10 = 0.00945 m o l 0.000945 \times 10 = 0.00945 \mathrm{ mol} 0.000945 × 10 = 0.00945 mol
Mass of pure N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 = 0.00945 × 106.0 = 1.002 g 0.00945 \times 106.0 = 1.002 \mathrm{ g} 0.00945 × 106.0 = 1.002 g
This is close to 100%, so let me use a different titre. With 15.0 cm3 ^3 3 :
Moles of H C l \mathrm{HCl} HCl used = 0.100 × 15.0 / 1000 = 0.00150 m o l 0.100 \times 15.0 / 1000 = 0.00150 \mathrm{ mol} 0.100 × 15.0/1000 = 0.00150 mol
Moles of N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 in 25.0 cm3 ^3 3 = 0.00150 / 2 = 0.000750 m o l 0.00150 / 2 = 0.000750 \mathrm{ mol} 0.00150/2 = 0.000750 mol
Moles of N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 in 250 cm3 ^3 3 = 0.000750 × 10 = 0.00750 m o l 0.000750 \times 10 = 0.00750 \mathrm{ mol} 0.000750 × 10 = 0.00750 mol
Mass of pure N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 = 0.00750 × 106.0 = 0.795 g 0.00750 \times 106.0 = 0.795 \mathrm{ g} 0.00750 × 106.0 = 0.795 g
% p u r i t y = 0.795 1.00 × 100 % = 79.5 % \%\mathrm{ purity} = \dfrac{0.795}{1.00} \times 100\% = 79.5\% % purity = 1.00 0.795 × 100% = 79.5%
Back titration is used when the substance being analysed reacts too slowly, is insoluble, or the Endpoint is hard to detect directly.
React the analyte with excess standard reagent. Titrate the remaining excess reagent with another standard solution. Worked example 16: 2.00 g of impure C a C O 3 \mathrm{CaCO}_3 CaCO 3 is reacted with 50.0 cm3 ^3 3 of 1.00 Mol/dm3 ^3 3 H C l \mathrm{HCl} HCl (excess). The remaining H C l \mathrm{HCl} HCl requires 30.0 cm3 ^3 3 of 0.500 Mol/dm3 ^3 3 N a O H \mathrm{NaOH} NaOH for neutralisation. Calculate the percentage of C a C O 3 \mathrm{CaCO}_3 CaCO 3 in the Sample.
C a C O 3 + 2 H C l → C a C l 2 + H 2 O + C O 2 \mathrm{CaCO}_3 + 2\mathrm{HCl} \to \mathrm{CaCl}_2 + \mathrm{H}_2\mathrm{O} + \mathrm{CO}_2 CaCO 3 + 2 HCl → CaCl 2 + H 2 O + CO 2 H C l + N a O H → N a C l + H 2 O \mathrm{HCl} + \mathrm{NaOH} \to \mathrm{NaCl} + \mathrm{H}_2\mathrm{O} HCl + NaOH → NaCl + H 2 O
Answer Total moles of H C l \mathrm{HCl} HCl added = 1.00 × 50.0 / 1000 = 0.0500 m o l 1.00 \times 50.0 / 1000 = 0.0500 \mathrm{ mol} 1.00 × 50.0/1000 = 0.0500 mol
Moles of N a O H \mathrm{NaOH} NaOH used = 0.500 × 30.0 / 1000 = 0.0150 m o l 0.500 \times 30.0 / 1000 = 0.0150 \mathrm{ mol} 0.500 × 30.0/1000 = 0.0150 mol
Moles of H C l \mathrm{HCl} HCl remaining = 0.0150 m o l 0.0150 \mathrm{ mol} 0.0150 mol (1:1 ratio)
Moles of H C l \mathrm{HCl} HCl reacted with C a C O 3 \mathrm{CaCO}_3 CaCO 3 = 0.0500 − 0.0150 = 0.0350 m o l 0.0500 - 0.0150 = 0.0350 \mathrm{ mol} 0.0500 − 0.0150 = 0.0350 mol
Moles of C a C O 3 \mathrm{CaCO}_3 CaCO 3 = 0.0350 / 2 = 0.0175 m o l 0.0350 / 2 = 0.0175 \mathrm{ mol} 0.0350/2 = 0.0175 mol
Mass of C a C O 3 \mathrm{CaCO}_3 CaCO 3 = 0.0175 × 100.1 = 1.752 g 0.0175 \times 100.1 = 1.752 \mathrm{ g} 0.0175 × 100.1 = 1.752 g
% C a C O 3 = 1.752 2.00 × 100 % = 87.6 % \%\mathrm{ CaCO}_3 = \dfrac{1.752}{2.00} \times 100\% = 87.6\% % CaCO 3 = 2.00 1.752 × 100% = 87.6%
m o l / d m 3 = g / d m 3 M r \mathrm{mol/dm}^3 = \frac{\mathrm{g/dm}^3}{M_r} mol/dm 3 = M r g/dm 3
p p m = m a s s o f s o l u t e ( g ) m a s s o f s o l u t i o n ( g ) × 10 6 \mathrm{ppm} = \frac{\mathrm{mass of solute (g)}}{\mathrm{mass of solution (g)}} \times 10^6 ppm = massofsolution ( g ) massofsolute ( g ) × 1 0 6
Worked example 17: Convert 20.0 g/dm3 ^3 3 of N a O H \mathrm{NaOH} NaOH to mol/dm3 ^3 3 .
Answer c = 20.0 / 40.0 = 0.500 m o l / d m 3 c = 20.0 / 40.0 = 0.500 \mathrm{ mol/dm}^3 c = 20.0/40.0 = 0.500 mol/dm 3
Worked example 18: 5.00 g of hydrated magnesium sulfate, M g S O 4 ⋅ x H 2 O \mathrm{MgSO}_4 \cdot x\mathrm{H}_2\mathrm{O} MgSO 4 ⋅ x H 2 O Is dissolved in water and made up to 250 cm3 ^3 3 . 25.0 cm3 ^3 3 of this solution requires 20.0 cm3 ^3 3 of 0.100 mol/dm3 ^3 3 N a O H \mathrm{NaOH} NaOH to precipitate All the magnesium as M g ( O H ) 2 \mathrm{Mg(OH)}_2 Mg ( OH ) 2 . Find x x x .
M g S O 4 + 2 N a O H → M g ( O H ) 2 + N a 2 S O 4 \mathrm{MgSO}_4 + 2\mathrm{NaOH} \to \mathrm{Mg(OH)}_2 + \mathrm{Na}_2\mathrm{SO}_4 MgSO 4 + 2 NaOH → Mg ( OH ) 2 + Na 2 SO 4
Answer Moles of N a O H \mathrm{NaOH} NaOH = 0.100 × 20.0 / 1000 = 0.00200 m o l 0.100 \times 20.0 / 1000 = 0.00200 \mathrm{ mol} 0.100 × 20.0/1000 = 0.00200 mol
Moles of M g S O 4 \mathrm{MgSO}_4 MgSO 4 in 25.0 cm3 ^3 3 = 0.00200 / 2 = 0.00100 m o l 0.00200 / 2 = 0.00100 \mathrm{ mol} 0.00200/2 = 0.00100 mol
Moles of M g S O 4 \mathrm{MgSO}_4 MgSO 4 in 250 cm3 ^3 3 = 0.00100 × 10 = 0.0100 m o l 0.00100 \times 10 = 0.0100 \mathrm{ mol} 0.00100 × 10 = 0.0100 mol
M r ( M g S O 4 ) = 24.3 + 32.1 + 4 ( 16.0 ) = 120.4 M_r(\mathrm{MgSO}_4) = 24.3 + 32.1 + 4(16.0) = 120.4 M r ( MgSO 4 ) = 24.3 + 32.1 + 4 ( 16.0 ) = 120.4
Mass of M g S O 4 \mathrm{MgSO}_4 MgSO 4 (anhydrous) = 0.0100 × 120.4 = 1.204 g 0.0100 \times 120.4 = 1.204 \mathrm{ g} 0.0100 × 120.4 = 1.204 g
Mass of water = 5.00 − 1.204 = 3.796 g 5.00 - 1.204 = 3.796 \mathrm{ g} 5.00 − 1.204 = 3.796 g
Moles of water = 3.796 / 18.0 = 0.211 m o l 3.796 / 18.0 = 0.211 \mathrm{ mol} 3.796/18.0 = 0.211 mol
x = 0.211 / 0.0100 = 21.1 x = 0.211 / 0.0100 = 21.1 x = 0.211/0.0100 = 21.1
This is unrealistic for magnesium sulfate. The expected value is x = 7 x = 7 x = 7 for Epsom salt. The data Likely has an issue. For M g S O 4 ⋅ 7 H 2 O \mathrm{MgSO}_4 \cdot 7\mathrm{H}_2\mathrm{O} MgSO 4 ⋅ 7 H 2 O : M r = 120.4 + 7 ( 18.0 ) = 246.4 M_r = 120.4 + 7(18.0) = 246.4 M r = 120.4 + 7 ( 18.0 ) = 246.4 . 5.00 g would give 5.00 / 246.4 = 0.0203 m o l 5.00/246.4 = 0.0203 \mathrm{ mol} 5.00/246.4 = 0.0203 mol And 25 Cm3 ^3 3 aliquot would need 0.00203 × 2 = 0.00406 m o l 0.00203 \times 2 = 0.00406 \mathrm{ mol} 0.00203 × 2 = 0.00406 mol N a O H \mathrm{NaOH} NaOH I.e. 40.6 Cm3 ^3 3 of 0.100 M NaOH.
Revised problem: using titre of 40.6 cm3 ^3 3 :
Moles of N a O H \mathrm{NaOH} NaOH = 0.100 × 40.6 / 1000 = 0.00406 m o l 0.100 \times 40.6 / 1000 = 0.00406 \mathrm{ mol} 0.100 × 40.6/1000 = 0.00406 mol
Moles of M g S O 4 \mathrm{MgSO}_4 MgSO 4 in 25.0 cm3 ^3 3 = 0.00406 / 2 = 0.00203 m o l 0.00406 / 2 = 0.00203 \mathrm{ mol} 0.00406/2 = 0.00203 mol
Moles in 250 cm3 ^3 3 = 0.0203 m o l 0.0203 \mathrm{ mol} 0.0203 mol
Mass of M g S O 4 \mathrm{MgSO}_4 MgSO 4 = 0.0203 × 120.4 = 2.444 g 0.0203 \times 120.4 = 2.444 \mathrm{ g} 0.0203 × 120.4 = 2.444 g
Mass of water = 5.00 − 2.444 = 2.556 g 5.00 - 2.444 = 2.556 \mathrm{ g} 5.00 − 2.444 = 2.556 g
Moles of water = 2.556 / 18.0 = 0.142 m o l 2.556 / 18.0 = 0.142 \mathrm{ mol} 2.556/18.0 = 0.142 mol
x = 0.142 / 0.0203 = 7.00 x = 0.142 / 0.0203 = 7.00 x = 0.142/0.0203 = 7.00
Therefore x = 7 x = 7 x = 7 Confirming the formula M g S O 4 ⋅ 7 H 2 O \mathrm{MgSO}_4 \cdot 7\mathrm{H}_2\mathrm{O} MgSO 4 ⋅ 7 H 2 O .
Chemical accounting: Stoichiometry is like a recipe — the balanced equation tells you exactly how much of each ingredient you need and how much product you’ll get. The mole is the chemist’s dozen.
Why it matters: From manufacturing drugs to calculating fuel efficiency, stoichiometry lets you predict quantities. Errors in stoichiometric calculations can be dangerous or wasteful.
The key insight: The mole concept bridges the gap between atoms (invisible) and grams (measurable) — Avogadro’s number is the conversion factor.
Confusing STP and RTP: STP molar volume is 22.4 dm3 ^3 3 /mol; RTP is 24.0 dm3 ^3 3 /mol. Always check the conditions stated in the question.
Forgetting to convert cm3 ^3 3 to dm3 ^3 3 : Divide cm3 ^3 3 by 1000 before using in c = n / V c = n/V c = n / V .
Using total mass instead of solute mass: When calculating molarity, use the mass of the solute only, not the total mass of the solution.
Incorrect mole ratios: Always use the balanced equation to determine mole ratios. Never assume a 1:1 ratio.
Choosing the wrong limiting reagent: Always calculate both reactants and compare. The one that produces less product is the limiting reagent.
Mixing up empirical and molecular formulae: The empirical formula is the simplest ratio; the molecular formula is a multiple of it.
Ignoring significant figures in titration: Burette readings should be recorded to 2 decimal places (e.g., 24.50 cm3 ^3 3 Not 24.5 cm3 ^3 3 ).
Forgetting the factor of 2 in back titrations: Account for the stoichiometry of both reactions involved.
A compound contains 36.5% sodium, 25.4% sulfur, and 38.1% oxygen by mass. Determine the empirical Formula and, given that the molar mass is 126 g/mol, the molecular formula.
Answer Element Mass (%) A r A_r A r Moles Ratio Na 36.5 23.0 36.5 / 23.0 = 1.587 1.587 / 0.793 = 2.00 S 25.4 32.1 25.4 / 32.1 = 0.791 0.791 / 0.793 = 0.997 O 38.1 16.0 38.1 / 16.0 = 2.381 2.381 / 0.793 = 3.00
Empirical formula = N a 2 S O 3 \mathrm{Na}_2\mathrm{SO}_3 Na 2 SO 3
M r ( N a 2 S O 3 ) = 2 ( 23.0 ) + 32.1 + 3 ( 16.0 ) = 126.1 M_r(\mathrm{Na}_2\mathrm{SO}_3) = 2(23.0) + 32.1 + 3(16.0) = 126.1 M r ( Na 2 SO 3 ) = 2 ( 23.0 ) + 32.1 + 3 ( 16.0 ) = 126.1
n = 126 / 126.1 = 1.00 n = 126 / 126.1 = 1.00 n = 126/126.1 = 1.00
Molecular formula = N a 2 S O 3 \mathrm{Na}_2\mathrm{SO}_3 Na 2 SO 3 (sodium sulfite)
25.0 cm3 ^3 3 of 0.200 mol/dm3 ^3 3 H 2 S O 4 \mathrm{H}_2\mathrm{SO}_4 H 2 SO 4 is completely neutralised by K O H \mathrm{KOH} KOH solution. If 40.0 cm3 ^3 3 of K O H \mathrm{KOH} KOH is required, what is the concentration of The K O H \mathrm{KOH} KOH ?
Answer H 2 S O 4 + 2 K O H → K 2 S O 4 + 2 H 2 O \mathrm{H}_2\mathrm{SO}_4 + 2\mathrm{KOH} \to \mathrm{K}_2\mathrm{SO}_4 + 2\mathrm{H}_2\mathrm{O} H 2 SO 4 + 2 KOH → K 2 SO 4 + 2 H 2 O
Moles of H 2 S O 4 \mathrm{H}_2\mathrm{SO}_4 H 2 SO 4 = 0.200 × 25.0 / 1000 = 0.00500 m o l 0.200 \times 25.0 / 1000 = 0.00500 \mathrm{ mol} 0.200 × 25.0/1000 = 0.00500 mol
Moles of K O H \mathrm{KOH} KOH = 0.00500 × 2 = 0.0100 m o l 0.00500 \times 2 = 0.0100 \mathrm{ mol} 0.00500 × 2 = 0.0100 mol
c ( K O H ) = 0.0100 / ( 40.0 / 1000 ) = 0.0100 / 0.0400 = 0.250 m o l / d m 3 c(\mathrm{KOH}) = 0.0100 / (40.0 / 1000) = 0.0100 / 0.0400 = 0.250 \mathrm{ mol/dm}^3 c ( KOH ) = 0.0100/ ( 40.0/1000 ) = 0.0100/0.0400 = 0.250 mol/dm 3
When 8.40 g of hydrated sodium carbonate, N a 2 C O 3 ⋅ x H 2 O \mathrm{Na}_2\mathrm{CO}_3 \cdot x\mathrm{H}_2\mathrm{O} Na 2 CO 3 ⋅ x H 2 O Is heated to constant mass, 3.10 g of Anhydrous N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 remains. Find the value of x x x .
Answer Mass of water lost = 8.40 − 3.10 = 5.30 g 8.40 - 3.10 = 5.30 \mathrm{ g} 8.40 − 3.10 = 5.30 g
Moles of N a 2 C O 3 \mathrm{Na}_2\mathrm{CO}_3 Na 2 CO 3 = 3.10 / 106.0 = 0.02925 m o l 3.10 / 106.0 = 0.02925 \mathrm{ mol} 3.10/106.0 = 0.02925 mol
Moles of H 2 O \mathrm{H}_2\mathrm{O} H 2 O = 5.30 / 18.0 = 0.2944 m o l 5.30 / 18.0 = 0.2944 \mathrm{ mol} 5.30/18.0 = 0.2944 mol
x = 0.2944 / 0.02925 = 10.07 ≈ 10 x = 0.2944 / 0.02925 = 10.07 \approx 10 x = 0.2944/0.02925 = 10.07 ≈ 10
Formula = N a 2 C O 3 ⋅ 10 H 2 O \mathrm{Na}_2\mathrm{CO}_3 \cdot 10\mathrm{H}_2\mathrm{O} Na 2 CO 3 ⋅ 10 H 2 O (washing soda)
2.43 g of magnesium is added to 100 cm3 ^3 3 of 2.00 mol/dm3 ^3 3 hydrochloric acid. Calculate the Volume of hydrogen gas produced at RTP and identify the limiting reagent.
M g + 2 H C l → M g C l 2 + H 2 \mathrm{Mg} + 2\mathrm{HCl} \to \mathrm{MgCl}_2 + \mathrm{H}_2 Mg + 2 HCl → MgCl 2 + H 2
Answer Moles of M g \mathrm{Mg} Mg = 2.43 / 24.3 = 0.100 m o l 2.43 / 24.3 = 0.100 \mathrm{ mol} 2.43/24.3 = 0.100 mol
Moles of H C l \mathrm{HCl} HCl = 2.00 × 100 / 1000 = 0.200 m o l 2.00 \times 100 / 1000 = 0.200 \mathrm{ mol} 2.00 × 100/1000 = 0.200 mol
Divide by coefficients: M g \mathrm{Mg} Mg : 0.100 / 1 = 0.100 0.100 / 1 = 0.100 0.100/1 = 0.100 , H C l \mathrm{HCl} HCl : 0.200 / 2 = 0.100 0.200 / 2 = 0.100 0.200/2 = 0.100
Both are in exactly the stoichiometric ratio. Neither is in strict excess; both are fully consumed.
Moles of H 2 \mathrm{H}_2 H 2 = 0.100 m o l 0.100 \mathrm{ mol} 0.100 mol (1:1 ratio with Mg)
Volume at RTP = 0.100 × 24.0 = 2.40 d m 3 0.100 \times 24.0 = 2.40 \mathrm{ dm}^3 0.100 × 24.0 = 2.40 dm 3
In a back titration, 0.500 g of limestone (C a C O 3 \mathrm{CaCO}_3 CaCO 3 ) is reacted with 40.0 cm3 ^3 3 of 0.500 Mol/dm3 ^3 3 H C l \mathrm{HCl} HCl . The excess H C l \mathrm{HCl} HCl requires 28.0 cm3 ^3 3 of 0.200 mol/dm3 ^3 3 N a O H \mathrm{NaOH} NaOH for neutralisation. Calculate the percentage of C a C O 3 \mathrm{CaCO}_3 CaCO 3 in the limestone.
Answer Total moles of H C l \mathrm{HCl} HCl = 0.500 × 40.0 / 1000 = 0.0200 m o l 0.500 \times 40.0 / 1000 = 0.0200 \mathrm{ mol} 0.500 × 40.0/1000 = 0.0200 mol
Moles of N a O H \mathrm{NaOH} NaOH = 0.200 × 28.0 / 1000 = 0.00560 m o l 0.200 \times 28.0 / 1000 = 0.00560 \mathrm{ mol} 0.200 × 28.0/1000 = 0.00560 mol
Moles of H C l \mathrm{HCl} HCl remaining = 0.00560 m o l 0.00560 \mathrm{ mol} 0.00560 mol
Moles of H C l \mathrm{HCl} HCl reacted with C a C O 3 \mathrm{CaCO}_3 CaCO 3 = 0.0200 − 0.00560 = 0.01440 m o l 0.0200 - 0.00560 = 0.01440 \mathrm{ mol} 0.0200 − 0.00560 = 0.01440 mol
Moles of C a C O 3 \mathrm{CaCO}_3 CaCO 3 = 0.01440 / 2 = 0.00720 m o l 0.01440 / 2 = 0.00720 \mathrm{ mol} 0.01440/2 = 0.00720 mol
Mass of C a C O 3 \mathrm{CaCO}_3 CaCO 3 = 0.00720 × 100.1 = 0.721 g 0.00720 \times 100.1 = 0.721 \mathrm{ g} 0.00720 × 100.1 = 0.721 g
% C a C O 3 = 0.721 0.500 × 100 % = 144 % \%\mathrm{ CaCO}_3 = \dfrac{0.721}{0.500} \times 100\% = 144\% % CaCO 3 = 0.500 0.721 × 100% = 144%
This is impossible. The issue is that with only 0.500 g of limestone, 40 cm3 ^3 3 of 0.500 M HCl is Far more than needed. Let me use more appropriate values.
Revised: 0.500 g limestone + 50.0 cm3 ^3 3 of 0.200 mol/dm3 ^3 3 HCl, excess requires 20.0 cm3 ^3 3 of 0.100 mol/dm3 ^3 3 NaOH.
Total moles of H C l \mathrm{HCl} HCl = 0.200 × 50.0 / 1000 = 0.01000 m o l 0.200 \times 50.0 / 1000 = 0.01000 \mathrm{ mol} 0.200 × 50.0/1000 = 0.01000 mol
Moles of N a O H \mathrm{NaOH} NaOH = 0.100 × 20.0 / 1000 = 0.00200 m o l 0.100 \times 20.0 / 1000 = 0.00200 \mathrm{ mol} 0.100 × 20.0/1000 = 0.00200 mol
Moles of H C l \mathrm{HCl} HCl remaining = 0.00200 m o l 0.00200 \mathrm{ mol} 0.00200 mol
Moles of H C l \mathrm{HCl} HCl reacted = 0.01000 − 0.00200 = 0.00800 m o l 0.01000 - 0.00200 = 0.00800 \mathrm{ mol} 0.01000 − 0.00200 = 0.00800 mol
Moles of C a C O 3 \mathrm{CaCO}_3 CaCO 3 = 0.00800 / 2 = 0.00400 m o l 0.00800 / 2 = 0.00400 \mathrm{ mol} 0.00800/2 = 0.00400 mol
Mass of C a C O 3 \mathrm{CaCO}_3 CaCO 3 = 0.00400 × 100.1 = 0.400 g 0.00400 \times 100.1 = 0.400 \mathrm{ g} 0.00400 × 100.1 = 0.400 g
% C a C O 3 = 0.400 0.500 × 100 % = 80.0 % \%\mathrm{ CaCO}_3 = \dfrac{0.400}{0.500} \times 100\% = 80.0\% % CaCO 3 = 0.500 0.400 × 100% = 80.0%
A student prepares 500 cm3 ^3 3 of 0.500 mol/dm3 ^3 3 H 2 S O 4 \mathrm{H}_2\mathrm{SO}_4 H 2 SO 4 by diluting Concentrated acid of density 1.84 g/cm3 ^3 3 containing 98.0% H 2 S O 4 \mathrm{H}_2\mathrm{SO}_4 H 2 SO 4 by mass. What volume of the concentrated acid is required?
Answer Moles of H 2 S O 4 \mathrm{H}_2\mathrm{SO}_4 H 2 SO 4 needed = 0.500 × 500 / 1000 = 0.250 m o l 0.500 \times 500 / 1000 = 0.250 \mathrm{ mol} 0.500 × 500/1000 = 0.250 mol
Mass of H 2 S O 4 \mathrm{H}_2\mathrm{SO}_4 H 2 SO 4 needed = 0.250 × 98.1 = 24.525 g 0.250 \times 98.1 = 24.525 \mathrm{ g} 0.250 × 98.1 = 24.525 g
Mass of concentrated acid = 24.525 / 0.980 = 25.03 g 24.525 / 0.980 = 25.03 \mathrm{ g} 24.525/0.980 = 25.03 g
Volume of concentrated acid = 25.03 / 1.84 = 13.6 c m 3 25.03 / 1.84 = 13.6 \mathrm{ cm}^3 25.03/1.84 = 13.6 cm 3
An organic compound contains only carbon, hydrogen, and oxygen. On complete combustion, 0.120 g of The compound produces 0.264 g of C O 2 \mathrm{CO}_2 CO 2 and 0.108 g of H 2 O \mathrm{H}_2\mathrm{O} H 2 O . Determine The empirical formula of the compound.
Answer Mass of C in C O 2 \mathrm{CO}_2 CO 2 = 0.264 × 12.0 44.0 = 0.0720 g 0.264 \times \dfrac{12.0}{44.0} = 0.0720 \mathrm{ g} 0.264 × 44.0 12.0 = 0.0720 g
Mass of H in H 2 O \mathrm{H}_2\mathrm{O} H 2 O = 0.108 × 2.0 18.0 = 0.0120 g 0.108 \times \dfrac{2.0}{18.0} = 0.0120 \mathrm{ g} 0.108 × 18.0 2.0 = 0.0120 g
Mass of O = 0.120 − 0.0720 − 0.0120 = 0.0360 g 0.120 - 0.0720 - 0.0120 = 0.0360 \mathrm{ g} 0.120 − 0.0720 − 0.0120 = 0.0360 g
Element Mass (g) A r A_r A r Moles Ratio C 0.0720 12.0 0.00600 1 H 0.0120 1.0 0.0120 2 O 0.0360 16.0 0.00225 0.375
Multiply all by 8 to clear the fraction: C : H : O = 8 : 16 : 3
Wait, 0.00225 / 0.00600 = 0.375 = 3 / 8 0.00225 / 0.00600 = 0.375 = 3/8 0.00225/0.00600 = 0.375 = 3/8 So multiply by 8:
C : H : O = 1 × 8 : 2 × 8 : 0.375 × 8 1 \times 8 : 2 \times 8 : 0.375 \times 8 1 × 8 : 2 × 8 : 0.375 × 8 = 8 : 16 : 3
Empirical formula = C 8 H 16 O 3 \mathrm{C}_8\mathrm{H}_{16}\mathrm{O}_3 C 8 H 16 O 3
Hmm, let me re-check. 0.375 × 8 = 3 0.375 \times 8 = 3 0.375 × 8 = 3 . So empirical formula = C 8 H 16 O 3 \mathrm{C}_8\mathrm{H}_{16}\mathrm{O}_3 C 8 H 16 O 3 .
But this seems large. Let me double check: 0.00600 / 0.00600 = 1 0.00600 / 0.00600 = 1 0.00600/0.00600 = 1 , 0.0120 / 0.00600 = 2 0.0120 / 0.00600 = 2 0.0120/0.00600 = 2 0.00225 / 0.00600 = 0.375 0.00225 / 0.00600 = 0.375 0.00225/0.00600 = 0.375 . Multiply by 8: 8, 16, 3. Yes, C 8 H 16 O 3 \mathrm{C}_8\mathrm{H}_{16}\mathrm{O}_3 C 8 H 16 O 3 .
Alternative approach with different ratios: multiply by 8 / 3 8/3 8/3 : 8 / 3 : 16 / 3 : 1 8/3 : 16/3 : 1 8/3 : 16/3 : 1 . No, that gives Fractions. The correct simplest integer ratio is indeed 8:16:3, giving C 8 H 16 O 3 \mathrm{C}_8\mathrm{H}_{16}\mathrm{O}_3 C 8 H 16 O 3 .
A[1_Mole Concept And Stoichiometry] --> B[Key Concepts]
A --> D[Practical Applications]
B --> E[Fundamental definitions]
D --> G[Real-world usage]
including key reactions, underlying theories, and practical applications.
Stashed changes:docs/docs_dse/Chemistry/mole-concept-and-stoichiometry.md
Key concepts include:
key chemical principles and theories mathematical relationships in chemistry practical techniques and apparatus applications of chemistry in industry environmental and ethical considerations Mastery of these concepts requires both theoretical understanding and the ability to apply knowledge to unfamiliar contexts, particularly in calculation and practical questions.
Stashed changes:docs/docs_dse/Chemistry/mole-concept-and-stoichiometry.md
Worked examples demonstrating the application of key concepts are covered in the detailed sub-pages linked above.