General Chemistry: cram pack

Formula sheets, the key method steps for every topic and 14 practice problems, with full solutions at the back.

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1Formulas and methods

Stoichiometry

Moles
n = m/M
Concentration
c = n/V
Mole ratio
use the coefficients of the balanced equation
Limiting reactant
the one that runs out first
Percent yield
actual / theoretical × 100%

Method

  1. Write and balance the chemical equation.
  2. Convert the given mass to moles: n = m/M.
  3. Use the coefficients as the mole ratio to find the moles of the substance you want.
  4. Convert back to mass with m = n·M. With two reactants, find the limiting reactant first.

Molarity & dilution

Molarity
c = n/V (mol/L)
Moles
n = m/M
Dilution
c1V1 = c2V2
Mixing
c = (c1V1 + c2V2)/(V1 + V2)

Method

  1. Convert mass to moles with n = m/M.
  2. Convert the volume to litres.
  3. Molarity c = n/V in mol/L.
  4. For a dilution, the moles stay the same: c₁V₁ = c₂V₂.

Ideal gas law

Ideal gas law
pV = nRT
Gas constant
R = 8.314 J/(mol·K)
Combined gas law
p1V1/T1 = p2V2/T2
Moles
n = m/M
Temperature
T[K] = T[°C] + 273.15

Calorimetry & enthalpy

Heat
q = m·c·ΔT
Water
c = 4.18 J/(g·°C)
Calorimeter
heat lost = heat gained
Enthalpy of reaction
ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants)

Chemical equilibrium

Equilibrium constant
Kc = [C]c[D]d/([A]a[B]b)
ICE table
Initial, Change (×coefficient), Equilibrium
Quadratic
x = (−b + √(b² − 4ac))/(2a)

Method

  1. Write Kc with products over reactants, each raised to the power of its coefficient.
  2. Set up an ICE table: Initial, Change (in steps of x times the coefficients), Equilibrium.
  3. Put the equilibrium expressions into Kc and solve for x.
  4. Check whether x is small enough for an approximation; otherwise solve the quadratic.

pH & buffers

pH
pH = −log[H⁺]
pOH
pOH = −log[OH⁻], pH + pOH = 14
Weak acid
[H⁺] ≈ √(Ka·c)
Buffer
pH = pKa + log([A⁻]/[HA])
Dilution
c1V1 = c2V2

Method

  1. Decide whether the acid or base is strong (fully dissociated) or weak.
  2. Strong acid: [H⁺] equals its concentration. Strong base: find [OH⁻] first.
  3. Weak acid: solve Ka = x²/(c − x) for x = [H⁺].
  4. pH = −log[H⁺], and pH + pOH = 14 at 25 °C.

Reaction kinetics

First order
ln(CA/CA0) = −kt
Half-life (first order)
t½ = ln 2/k
Second order
1/CA = 1/CA0 + kt
Arrhenius
k = A·e−Ea/(RT)
Two temperatures
ln(k2/k1) = (Ea/R)(1/T1 − 1/T2)

2Practice problems

1.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 3/ν× M(CO2​)

4 g of C3H8 and 10 g of O2 react according to C3H8 + 5O2 → 3CO2 + 4H2O. What mass m of CO2 can form?

M(C3H8) = 44.1M(O2) = 32M(CO2) = 44.01 g/mol
m = g
2.StoichiometryHard
m(Mg)n(Mg)n(MgO)m(MgO)÷ M(Mg)× 2/2× M(MgO)

In the reaction 2Mg + O2 → 2MgO, 6 g of Mg reacts completely (the other reactants are in excess) and 5.47 g of MgO is collected. Find the percent yield Y.

M(Mg) = 24.31 g/molM(MgO) = 40.3 g/molactual: 5.47 g
Y = %
3.Molarity & dilutionMedium
1.5 mol/LV1​ = ?0.4 mol/L1000 mL

You need 1000 mL of 0.4 mol/L solution and have a 1.5 mol/L stock solution. What volume V1 of stock solution do you need?

c1 = 1.5 mol/Lc2 = 0.4 mol/LV2 = 1000 mL
V1 = mL
4.Molarity & dilutionHard
1 mol/L200 mL0.3 mol/L500 mLc = ?700 mL

200 mL of a 1 mol/L solution is mixed with 500 mL of a 0.3 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 1 mol/LV1 = 200 mLc2 = 0.3 mol/LV2 = 500 mL
c = mol/L
5.Ideal gas lawMedium
220 g of CO₂P = 750 kPaT = 0 °CV = ?

What volume V does 220 g of CO₂ occupy at 750 kPa and 0 °C? Treat it as an ideal gas.

m = 220 gM = 44.01 g/molP = 750 kPaT = 0 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of CH₄ goes from 250 kPa, 5 L, 40 °C to 300 kPa and 250 °C. Find the new volume V2.

P1 = 250 kPaV1 = 5 LT1 = 40 °CP2 = 300 kPaT2 = 250 °C
V2 = L
7.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 250 gT = 120 °Cc = 0.449 J/(g·°C)Waterm = 300 gT = 22 °Cc = 4.18 J/(g·°C)

A 250 g block of iron (c = 0.449 J/(g·°C)) at 120 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 22 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.449 J/(g·°C)Tmetal = 120 °Cmwater = 300 gTwater = 22 °Ccwater = 4.18 J/(g·°C)
Tf = °C
8.Calorimetry & enthalpyHard
HC6​H12​O6​ + 6O₂reactants6CO₂ + 6H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l).

ΔH°f(C6H12O6) = −1274 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
ΔH° = kJ
9.Chemical equilibriumMedium
H2​I2​HII0.50.50C−x−x+2xE0.5 − x0.5 − x2x

0.5 mol/L of H₂ and 0.5 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 64. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 64
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I1.500C−x+x+xE1.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.5 at the reaction temperature. A container starts with 1.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 1.5 mol/LKc = 0.5
[Cl2] = mol/L
11.pH & buffersMedium
02468101214acidicneutralbasicpH = ?

Find the pH pH of a 0.5 mol/L solution of benzoic acid (Ka = 6.3 × 10⁻⁵).

c = 0.5 mol/LKa = 6.3 × 10⁻⁵
pH =
12.pH & buffersHard
02468101214acidicneutralbasicpH = ?

A 1.00 L buffer contains 0.3 mol lactic acid and 0.15 mol of its conjugate base (Ka = 0.00014). 0.01 mol of NaOH is added. Find the new pH pH.

n(HA) = 0.3 moln(A⁻) = 0.15 moln(OH⁻) = 0.01 molKa = 0.00014
pH =
13.Reaction kineticsMedium
t (min)X (%)t = ?60%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.4 L/(mol·min) and starts at 2 mol/L. How long does it take to reach 60% conversion? Find t.

k = 0.4 L/(mol·min)CA0 = 2 mol/LX = 60 %
t = min
14.Reaction kineticsHard
Tk20 °C0.145 °C?

A reaction has a rate constant of 0.1 min⁻¹ at 20 °C and an activation energy of 60 kJ/mol. Find the rate constant k2 at 45 °C.

k1 = 0.1 min⁻¹T1 = 20 °CT2 = 45 °CEa = 60 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹

3Solutions

1.Stoichiometry

Answer: m = 8.252 g

Stoichiometry: a balanced equation counts particles, not grams. Convert mass to moles with n = m/M, use the coefficients of the equation as the mole ratio, then convert back with m = n·M. With two reactants, the limiting reactant is the one that runs out first and fixes how much product forms.

Moles of each reactant

n(C3H8) = 4/44.1 = 0.0907 mol
n(O2) = 10/32 = 0.3125 mol

Limiting reactant

0.0907/1 = 0.0907, 0.3125/5 = 0.0625 → O2

Mass of product

n(CO2) = 0.0625·3 = 0.1875 mol
m = 0.1875·44.01 = 8.252 g

Answer

m = 8.252 g
2.Stoichiometry

Answer: Y = 54.99 %

Stoichiometry: a balanced equation counts particles, not grams. Convert mass to moles with n = m/M, use the coefficients of the equation as the mole ratio, then convert back with m = n·M. With two reactants, the limiting reactant is the one that runs out first and fixes how much product forms.

Theoretical yield

n(Mg) = 6/24.31 = 0.2468 mol
m = 0.2468·2/2·40.3 = 9.947 g

Percent yield

Y = 5.47/9.947·100 = 54.99%

Answer

Y = 54.99%
3.Molarity & dilution

Answer: V1 = 266.7 mL

Molarity: concentration c = n/V in mol/L, with n = m/M. Diluting adds solvent but not solute, so the number of moles stays the same: c₁·V₁ = c₂·V₂. When two solutions of the same solute are mixed, the moles add up and so do the volumes.

Volume of stock solution

V1 = c2·V2/c1 = 0.4·1000/1.5 = 266.7 mL

Answer

V1 = 266.7 mL
4.Molarity & dilution

Answer: c = 0.5 mol/L

Molarity: concentration c = n/V in mol/L, with n = m/M. Diluting adds solvent but not solute, so the number of moles stays the same: c₁·V₁ = c₂·V₂. When two solutions of the same solute are mixed, the moles add up and so do the volumes.

Total amount

n = 1·200 + 0.3·500 = 350 mmol

Concentration of the mixture

c = 350/700 = 0.5 mol/L

Answer

c = 0.5 mol/L
5.Ideal gas law

Answer: V = 15.14 L

Ideal gas law: PV = nRT, with n = m/M.

Moles

n = 220/44.01 = 4.999 mol
T = 0 + 273.15 = 273.1 K

Volume

V = nRT/P = 4.999·8.314·273.1/750 = 15.14 L

Answer

V = 15.14 L
6.Ideal gas law

Answer: V2 = 6.961 L

Combined gas law: for a fixed amount of ideal gas, P1V1/T1 = P2V2/T2.

Absolute temperatures

T1 = 313.1 K, T2 = 523.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(250/300)·(523.1/313.1) = 6.961 L

Answer

V2 = 6.961 L
7.Calorimetry & enthalpy

Answer: Tf = 30.05 °C

Heat and enthalpy: heating a substance takes q = m·c·ΔT. In a calorimeter the heat lost by the hot object equals the heat gained by the cold one. The enthalpy change of a reaction follows from enthalpies of formation: ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants), each multiplied by its coefficient.

Heat balance

250·0.449·(120 − Tf) = 300·4.18·(Tf − 22)

Solve for the final temperature

Tf = (112.3·120 + 1254·22)/(112.3 + 1254) = 30.05 °C

Answer

Tf = 30.05 °C
8.Calorimetry & enthalpy

Answer: ΔH° = −2802 kJ

Heat and enthalpy: heating a substance takes q = m·c·ΔT. In a calorimeter the heat lost by the hot object equals the heat gained by the cold one. The enthalpy change of a reaction follows from enthalpies of formation: ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants), each multiplied by its coefficient.

Enthalpy of reaction

ΔH° = [6·(−393.5) + 6·(−285.8)] − [1·(−1274) + 6·0] = −2802 kJ

Answer

ΔH° = −2802 kJ

Negative: the reaction gives off heat (exothermic).

9.Chemical equilibrium

Answer: [HI] = 0.8 mol/L

Chemical equilibrium: for aA + bB ⇌ cC + dD, the equilibrium constant is Kc = [C]c[D]d/([A]a[B]b), using concentrations at equilibrium. An ICE table (Initial, Change, Equilibrium) links the starting amounts to the equilibrium amounts through one unknown x, scaled by the coefficients.

Equilibrium expression

64 = (2x)²/(0.5 − x)²

Take the square root

8 = 2x/(0.5 − x) → x = 0.5·8/(2 + 8) = 0.4 mol/L

Equilibrium concentration

[HI] = 2x = 0.8 mol/L

Answer

[HI] = 0.8 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.6514 mol/L

Chemical equilibrium: for aA + bB ⇌ cC + dD, the equilibrium constant is Kc = [C]c[D]d/([A]a[B]b), using concentrations at equilibrium. An ICE table (Initial, Change, Equilibrium) links the starting amounts to the equilibrium amounts through one unknown x, scaled by the coefficients.

Equilibrium expression

0.5 = x²/(1.5 − x) → x² + 0.5·x − 0.75 = 0

Solve the quadratic

x = (−0.5 + √(0.5² + 4·0.75))/2 = 0.6514 mol/L

Equilibrium concentration

[Cl₂] = x = 0.6514 mol/L

Answer

[Cl2] = 0.6514 mol/L
11.pH & buffers

Answer: pH = 2.253

pH: pH = −log₁₀[H₃O⁺] and pOH = −log₁₀[OH⁻], with pH + pOH = 14 at 25 °C. Strong acids and bases ionise completely. A weak acid only partly: Ka = x²/(c − x), where x = [H₃O⁺]. A buffer of a weak acid and its conjugate base follows Henderson–Hasselbalch: pH = pKa + log([A⁻]/[HA]).

Equilibrium

HA ⇌ H⁺ + A⁻: x mol/L of acid ionises.

Ka = x²/(0.5 − x) → x = 0.005581 mol/L

pH

pH = −log(0.005581) = 2.253

Answer

pH = 2.253
12.pH & buffers

Answer: pH = 3.596

pH: pH = −log₁₀[H₃O⁺] and pOH = −log₁₀[OH⁻], with pH + pOH = 14 at 25 °C. Strong acids and bases ionise completely. A weak acid only partly: Ka = x²/(c − x), where x = [H₃O⁺]. A buffer of a weak acid and its conjugate base follows Henderson–Hasselbalch: pH = pKa + log([A⁻]/[HA]).

Neutralisation

n(HA) = 0.3 − 0.01 = 0.29 mol
n(A⁻) = 0.15 + 0.01 = 0.16 mol

Henderson–Hasselbalch

pH = 3.854 + log(0.16/0.29) = 3.596

Answer

pH = 3.596
13.Reaction kinetics

Answer: t = 1.875 min

Integrated rate laws: zero order: C = C₀ − kt (straight line, t½ = C₀/(2k)); first order: ln(C₀/C) = kt (t½ = ln 2/k); second order: 1/C − 1/C₀ = kt (t½ = 1/(kC₀)). Conversion X means C = C₀(1 − X).

Concentration at the end

CA = 2·(1 − 0.6) = 0.8 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (1.25 − 0.5)/0.4 = 1.875 min

Answer

t = 1.875 min
14.Reaction kinetics

Answer: k2 = 0.692 min⁻¹

Reaction rates: for a first-order reaction −dC/dt = kC, so C = C₀·e−kt and the half-life ln 2/k does not depend on concentration. For a second-order reaction 1/C = 1/C₀ + kt. The rate constant rises with temperature following Arrhenius: k = A·e−Ea/(RT).

Absolute temperatures

T1 = 293.1 K, T2 = 318.1 K

Arrhenius ratio

ln(k2/k1) = −(60000/8.314)·(1/318.1 − 1/293.1) = 1.934
k2 = 0.1·e1.934 = 0.692 min⁻¹

Answer

k2 = 0.692 min⁻¹

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