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(MgO)m(MgO)÷ M(X)× 2/ν× M(MgO)

30 g of Mg and 48 g of O2 react according to 2Mg + O2 → 2MgO. What mass m of MgO can form?

M(Mg) = 24.31M(O2) = 32M(MgO) = 40.3 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, 30 g of Mg reacts completely (the other reactants are in excess) and 27.35 g of MgO is collected. Find the percent yield Y.

M(Mg) = 24.31 g/molM(MgO) = 40.3 g/molactual: 27.35 g
Y = %
3.Molarity & dilutionMedium
1.5 mol/LV1​ = ?0.4 mol/L250 mL

You need 250 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 = 250 mL
V1 = mL
4.Molarity & dilutionHard
0.25 mol/L250 mL2.5 mol/L400 mLc = ?650 mL

250 mL of a 0.25 mol/L solution is mixed with 400 mL of a 2.5 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 0.25 mol/LV1 = 250 mLc2 = 2.5 mol/LV2 = 400 mL
c = mol/L
5.Ideal gas lawMedium
470 g of O₂P = 150 kPaT = 10 °CV = ?

What volume V does 470 g of O₂ occupy at 150 kPa and 10 °C? Treat it as an ideal gas.

m = 470 gM = 32 g/molP = 150 kPaT = 10 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of Ar goes from 200 kPa, 2 L, 40 °C to 650 kPa and 200 °C. Find the new volume V2.

P1 = 200 kPaV1 = 2 LT1 = 40 °CP2 = 650 kPaT2 = 200 °C
V2 = L
7.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 50 gT = 190 °Cc = 0.129 J/(g·°C)Waterm = 250 gT = 17 °Cc = 4.18 J/(g·°C)

A 50 g block of lead (c = 0.129 J/(g·°C)) at 190 °C is dropped into 250 g of water (c = 4.18 J/(g·°C)) at 17 °C in an insulated cup. Find the final temperature Tf.

mmetal = 50 gcmetal = 0.129 J/(g·°C)Tmetal = 190 °Cmwater = 250 gTwater = 17 °Ccwater = 4.18 J/(g·°C)
Tf = °C
8.Calorimetry & enthalpyHard
H50 g C3​H8​C3​H8​ + 5O₂reactants3CO₂ + 4H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 g of C3H8 (M = 44.1 g/mol) burns completely: C3H8 + 5O₂ → 3CO₂ + 4H₂O(l). Give q as a positive number.

ΔH°f(C3H8) = −103.8 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
q = 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 = 49. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 49
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.800C−x+x+xE0.8 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 at the reaction temperature. A container starts with 0.8 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.8 mol/LKc = 0.1
[Cl2] = mol/L
11.pH & buffersMedium
02468101214acidicneutralbasicpH = ?

Find the pH pH of a 0.1 mol/L solution of hypochlorous acid (Ka = 3 × 10⁻⁸).

c = 0.1 mol/LKa = 3 × 10⁻⁸
pH =
12.pH & buffersHard
02468101214acidicneutralbasicpH = ?

A buffer contains 0.4 mol/L hydrofluoric acid and 0.5 mol/L of its sodium salt. Ka = 0.00068. Find the pH pH of the buffer.

[HA] = 0.4[A⁻] = 0.5Ka = 0.00068
pH =
13.Reaction kineticsMedium
t (min)C (mol/L)15 min0.25

In a first-order reaction the concentration of A falls from 0.5 mol/L to 0.25 mol/L in 15 min. Find the rate constant k.

CA0 = 0.5 mol/LCA = 0.25 mol/Lt = 15 min
k = min⁻¹
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.10.01run 20.20.02n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.1 mol/L the rate is 0.01 mol/(L·s); with CA0 = 0.2 mol/L it is 0.02 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.1 mol/Lr1 = 0.01 mol/(L·s)CA0,2 = 0.2 mol/Lr2 = 0.02 mol/(L·s)
n =

3Solutions

1.Stoichiometry

Answer: m = 49.73 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(Mg) = 30/24.31 = 1.234 mol
n(O2) = 48/32 = 1.5 mol

Limiting reactant

1.234/2 = 0.617, 1.5/1 = 1.5 → Mg

Mass of product

n(MgO) = 0.617·2 = 1.234 mol
m = 1.234·40.3 = 49.73 g

Answer

m = 49.73 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) = 30/24.31 = 1.234 mol
m = 1.234·2/2·40.3 = 49.73 g

Percent yield

Y = 27.35/49.73·100 = 54.99%

Answer

Y = 54.99%
3.Molarity & dilution

Answer: V1 = 66.67 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 = 0.4·250/1.5 = 66.67 mL

Answer

V1 = 66.67 mL
4.Molarity & dilution

Answer: c = 1.635 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 = 0.25·250 + 2.5·400 = 1063 mmol

Concentration of the mixture

c = 1063/650 = 1.635 mol/L

Answer

c = 1.635 mol/L
5.Ideal gas law

Answer: V = 230.5 L

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

Moles

n = 470/32 = 14.69 mol
T = 10 + 273.15 = 283.1 K

Volume

V = nRT/P = 14.69·8.314·283.1/150 = 230.5 L

Answer

V = 230.5 L
6.Ideal gas law

Answer: V2 = 0.9298 L

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

Absolute temperatures

T1 = 313.1 K, T2 = 473.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 2·(200/650)·(473.1/313.1) = 0.9298 L

Answer

V2 = 0.9298 L
7.Calorimetry & enthalpy

Answer: Tf = 18.06 °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

50·0.129·(190 − Tf) = 250·4.18·(Tf − 17)

Solve for the final temperature

Tf = (6.45·190 + 1045·17)/(6.45 + 1045) = 18.06 °C

Answer

Tf = 18.06 °C
8.Calorimetry & enthalpy

Answer: q = 2517 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° = [3·(−393.5) + 4·(−285.8)] − [1·(−103.8) + 5·0] = −2220 kJ

Heat for the given mass

n = 50/44.1 = 1.134 mol
q = n·|ΔH°/1| = 1.134·2220 = 2517 kJ

Answer

q = 2517 kJ
9.Chemical equilibrium

Answer: [HI] = 0.7778 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

49 = (2x)²/(0.5 − x)²

Take the square root

7 = 2x/(0.5 − x) → x = 0.5·7/(2 + 7) = 0.3889 mol/L

Equilibrium concentration

[HI] = 2x = 0.7778 mol/L

Answer

[HI] = 0.7778 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.2372 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

0.1 = x²/(0.8 − x) → x² + 0.1·x − 0.08 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.08))/2 = 0.2372 mol/L

Equilibrium concentration

[Cl₂] = x = 0.2372 mol/L

Answer

[Cl2] = 0.2372 mol/L
11.pH & buffers

Answer: pH = 4.262

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/(0.1 − x) → x = 5.476 × 10⁻⁵ mol/L

pH

pH = −log(5.476 × 10⁻⁵) = 4.262

Answer

pH = 4.262
12.pH & buffers

Answer: pH = 3.264

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]).

pKa

pKa = 3.167

Henderson–Hasselbalch

pH = 3.167 + log(0.5/0.4) = 3.264

Answer

pH = 3.264
13.Reaction kinetics

Answer: k = 0.04621 min⁻¹

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).

Integrated first-order law

k = ln(CA0/CA)/t = ln(0.5/0.25)/15 = 0.6931/15 = 0.04621 min⁻¹

Answer

k = 0.04621 min⁻¹
14.Reaction kinetics

Answer: n = 1

Method of initial rates: for r = k·Cⁿ, comparing two runs that differ only in the starting concentration removes k: r₂/r₁ = (C₂/C₁)ⁿ. Doubling C doubles the rate for first order and quadruples it for second order.

Ratios

r2/r1 = 0.02/0.01 = 2
C2/C1 = 0.2/0.1 = 2

Order

n = ln(2)/ln(2) = 1

Answer

n = 1

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