Energy, rates, equilibrium, acids, cells and solutions

Grade 12 Chemistry

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Thermochemistry

  • L1
    Lesson 1
    Counting particles
    grams → moles → molecules, before any heat arrives

    Thermochemistry measures energy PER MOLE, so every problem this chapter opens the same way: turn what you weighed into what you counted.

    The formula in this lesson
    n=mMn = \dfrac{m}{M}
  • L2
    Lesson 2
    Heat in the cup
    ΔT is a difference, not a reading

    The Greek delta is said delta, and it means final minus initial — always in that order, every time it appears. Two consequences of that order, and the exam lives on both.

    The formula in this lesson
    Q=mcΔTQ = m c \Delta T
  • L3
    Lesson 3
    Warming and melting
    the heating curve · slopes take mcΔT, plateaus take mL

    Heat a beaker of ice steadily and plot temperature against time. The graph is not a ramp — it is a staircase of slopes and plateaus, and each kind of segment has its own machine.

    The formulas in this lesson
    Q=mLQ = m L,Q=mcΔTQ = m c \Delta T
  • L4
    Lesson 4
    Heat per mole
    Why exothermic is negative

    A calorimeter reports joules. A data table reports kilojoules per mole.

    The formula in this lesson
    q=n ΔHq = n\,\Delta H
  • L5
    Lesson 5
    The coffee cup
    two formulas in one chain · heat from the water, moles from the solution

    A coffee-cup calorimeter is a polystyrene cup, a lid and a thermometer, and it measures enthalpy changes by refusing to let heat escape.

    The formula in this lesson
    Q=mcΔTQ = m c \Delta T
  • L6
    Lesson 6
    The ladder of Hess
    route a reaction through steps you already know

    Some reactions cannot be run cleanly in a calorimeter — you cannot burn carbon and get pure carbon monoxide, and nobody makes acetylene from graphite by asking nicely.

    The formula in this lesson
    ΔHrxn=ΔH1+ΔH2+ΔH3\Delta H_{\text{rxn}} = \Delta H_1 + \Delta H_2 + \Delta H_3
  • L7
    Lesson 7
    The formation shortcut
    ΔH°f tables · products minus reactants, in that order

    Routing every reaction by hand would be exhausting, so chemistry tabulated the routes once.

    The formula in this lesson
    ΔHrxn∘=∑ΔHf∘(prod)−∑ΔHf∘(react)\Delta H^{\circ}_{\text{rxn}} = \sum \Delta H^{\circ}_{f}(\text{prod}) - \sum \Delta H^{\circ}_{f}(\text{react})
  • ★
    Boss lesson
    The Heat Audit
    the boss · no calculator · mass to moles to a verdict

    One pellet, one long problem, and every answer feeds the next: grams to moles, moles to kilojoules, kilojoules to joules, joules to a temperature rise — and then the line that actually matters, whether the run passes its specification.

Rates & Kinetics

  • L9
    Lesson 9
    Reading the rate law
    the order is an exponent you MEASURE

    Equilibrium asked where a reaction ends up. Kinetics asks something the balanced equation cannot answer: how FAST it gets there.

    The formula in this lesson
    r=k [A]nr = k\,[\mathrm{A}]^{n}
  • L10
    Lesson 10
    Arrhenius and the hill
    Kelvin only, joules only

    Molecules collide constantly and mostly bounce. A reaction happens only when a collision arrives with enough energy to climb the activation energy — the hill between reactants and products.

    The formula in this lesson
    k=A e−Ea/RTk = A\,e^{-E_a/RT}
  • L11
    Lesson 11
    Two temperatures
    Ea from a pair of runs — or from the plot's slope

    Let the units keep you honest one way only — if they refuse to cancel into J/mol the rearrangement is wrong, no appeal; units that do work out never prove you right.

    The formulas in this lesson
    ln⁡k2k1=EaR(1T1−1T2)\ln\dfrac{k_2}{k_1} = \dfrac{E_a}{R}\left(\dfrac{1}{T_1} - \dfrac{1}{T_2}\right),Ea=−R×slopeE_a = -R \times \text{slope}
  • L12
    Lesson 12
    Straight-line decay
    zero order falls in a line, first order in a curve

    A rate law tells you the speed right now. Integrate it over a clock and you get the concentration ITSELF at any time — an integrated rate law.

    The formulas in this lesson
    [A]=[A]0−kt[\mathrm{A}] = [\mathrm{A}]_0 - kt,[A]=[A]0 e−kt[\mathrm{A}] = [\mathrm{A}]_0\,e^{-kt}
  • L13
    Lesson 13
    The half-life clock
    Then count the halvings

    Ask a first-order reaction how long it takes to lose HALF of itself and something remarkable falls out.

    The formulas in this lesson
    t1/2=ln⁡2kt_{1/2} = \dfrac{\ln 2}{k},N=N0(12)t/t1/2N = N_0\left(\tfrac{1}{2}\right)^{t/t_{1/2}}
  • L14
    Lesson 14
    Second-order slowdown
    1/[A] climbs · and every half-life is longer than the last

    A second-order step needs two molecules in the same place at the same instant. As the reactant thins, those meetings get rare fast — so a second-order reaction does not just slow down, it slows down and then slows down again.

    The formulas in this lesson
    1[A]=1[A]0+kt\dfrac{1}{[\mathrm{A}]} = \dfrac{1}{[\mathrm{A}]_0} + kt,t1/2=1k [A]0t_{1/2} = \dfrac{1}{k\,[\mathrm{A}]_0}
  • ★
    Boss lesson
    The Rate Tribunal
    the boss · no calculator · read it, warm it, run the clock

    One tank, one long problem, and every answer feeds the next: the rate constant from the logged rate, then the warmed constant, then the half-life it buys, then what survives the hold — and finally the only thing the plant actually cares…

Chemical Equilibrium

  • L16
    Lesson 16
    Writing K
    products over reactants — and who never shows up

    A reversible reaction does not stop; it gets BORED. Forward and reverse settle at the same speed, the concentrations stop drifting, and the mixture sits there looking still while both reactions run flat out underneath.

    The formula in this lesson
    Kc=[C][D][A][B]K_c = \dfrac{[\mathrm{C}][\mathrm{D}]}{[\mathrm{A}][\mathrm{B}]}
  • L17
    Lesson 17
    Q against K
    the same expression, measured too early — and what it predicts

    Here is the trick that makes equilibrium predictive rather than merely descriptive.

    The formula in this lesson
    Q=[C]c[A]a[B]bQ = \dfrac{[\mathrm{C}]^{c}}{[\mathrm{A}]^{a}[\mathrm{B}]^{b}}
  • L18
    Lesson 18
    Kp meets Kc
    (RT)^Δn · the crossing from concentrations to pressures

    Gases can be counted two ways: by concentration in mol/L, or by the pressure they push with. The ideal gas law joins them in one line.

    The formulas in this lesson
    Kp=Kc(RT)ΔnK_p = K_c (RT)^{\Delta n},Kc=Kp(RT)ΔnK_c = \dfrac{K_p}{(RT)^{\Delta n}}
  • L19
    Lesson 19
    Sparingly soluble
    Ksp · s² against 4s³ · and why the smaller Ksp can win

    Drop a spoon of silver chloride into water and almost nothing dissolves — but not NOTHING.

    The formulas in this lesson
    Ksp=4s3K_{sp} = 4s^{3},Ksp=s2K_{sp} = s^{2}
  • L20
    Lesson 20
    Gibbs decides
    ΔG = ΔH − TΔS, and the bridge ΔG° = −RT ln K

    Two urges argue in every reaction. Energy wants to go downhill — that is enthalpy. Matter wants to spread out — that is entropy.

    The formulas in this lesson
    ΔG=ΔH−T ΔS\Delta G = \Delta H - T\,\Delta S,ΔG∘=−RTln⁡K\Delta G^{\circ} = -RT\ln K
  • ★
    Boss lesson
    The Position of Equilibrium
    the boss · no calculator · one converter, every tool in the chapter

    Chemists have used that shortcut for a century; today you get to.

Acids & Bases

  • L22
    Lesson 22
    The pH scale
    p is an operator · pH, pOH, and the ruler they share

    Grade 11 taught you to read a pH. Grade 12 asks what the symbol MEANS, because the same move is about to be played on four other quantities.

    The formulas in this lesson
    pH=−log⁡[H+]\mathrm{pH} = -\log[\mathrm{H^+}],pH+pOH=14\mathrm{pH} + \mathrm{pOH} = 14
  • L23
    Lesson 23
    The Kw family
    Ka, Kb, Kw · and the p-scale that flattens them

    Those two are not independent.

    The formulas in this lesson
    pKa=−log⁡Ka\mathrm{p}K_a = -\log K_a,KaKb=KwK_a K_b = K_w,pKa+pKb=14\mathrm{p}K_a + \mathrm{p}K_b = 14
  • L24
    Lesson 24
    Weak acids and ICE
    pH from Ka and C · and how much actually let go

    Put a weak acid in water and set up an ICE table — Initial, Change, Equilibrium. Call the formal concentration C: the amount you actually made up, in mol/L, before any proton moved.

    The formulas in this lesson
    pH=−12log⁡(KaC)\mathrm{pH} = -\tfrac{1}{2}\log(K_a C),% ion=[H+]C×100%\%\,\mathrm{ion} = \dfrac{[\mathrm{H^+}]}{C} \times 100\%
  • L25
    Lesson 25
    Buffer country
    Henderson–Hasselbalch · the pair's ratio sets the pH

    A buffer holds a weak acid AND its conjugate base in the same flask, so acid added is mopped up by the base and base added is mopped up by the acid.

    The formulas in this lesson
    pH=pKa+log⁡[A−][HA]\mathrm{pH} = \mathrm{p}K_a + \log\dfrac{[\mathrm{A^-}]}{[\mathrm{HA}]},pOH=pKb+log⁡[BH+][B]\mathrm{pOH} = \mathrm{p}K_b + \log\dfrac{[\mathrm{BH^+}]}{[\mathrm{B}]}
  • L26
    Lesson 26
    Dilution discipline
    Final volume, never added volume

    Not the volume of solvent you poured: the volume of what is in the flask when you stop.

    The formulas in this lesson
    C=nVC = \dfrac{n}{V},C1V1=C2V2C_1 V_1 = C_2 V_2
  • L27
    Lesson 27
    The burette
    titration · the mole ratio referees · mL cancels, until it doesn't

    A titration measures a concentration you cannot see by reacting it away against one you can. A pipetted aliquot of the unknown acid waits in the flask; standard base drips from the burette until the indicator turns.

    The formula in this lesson
    CaVa=n CbVbC_a V_a = n\,C_b V_b
  • ★
    Boss lesson
    The Titration Final
    the boss · no calculator · dilute it, titrate it, then rule on it

    One bench runs the whole unit: the volumetric flask dilutes the titrant, the burette finds the acid, the log places it on the scale, the see-saw hands over the other end — and every answer feeds the next line.

    The formula in this lesson
    C1V1=C2V2C_1 V_1 = C_2 V_2

Electrochemistry

  • L29
    Lesson 29
    Reading the table
    which half-cell is the cathode, and what the cell is worth

    Every electrochemistry data sheet you will ever be handed prints its half-reactions as reductions — electrons on the left, going in.

    The formula in this lesson
    Ecell∘=Ecat∘−Ean∘E^{\circ}_{\text{cell}} = E^{\circ}_{\text{cat}} - E^{\circ}_{\text{an}}
  • L30
    Lesson 30
    Nernst, off standard
    what the cell is worth once the bath drifts

    A real cell leaves those conditions the instant it starts working — it eats its reactants.

    The formula in this lesson
    E=E∘−0.0592nlog⁡QE = E^{\circ} - \dfrac{0.0592}{n}\log Q
  • L31
    Lesson 31
    Charge on the clock
    The seconds the formula insists on

    An ampere is not a substance that flows; it is a rate. One ampere is one coulomb per second.

    The formula in this lesson
    Q=ItQ = It
  • L32
    Lesson 32
    Faraday's scales
    Coulombs weighed as grams

    Name every letter before it works. m is the mass deposited at the electrode, in grams. Q is the charge passed, in coulombs. M is the molar mass of the element plating out, in grams per mole. F is the Faraday constant, 96500 C/mol — the…

    The formula in this lesson
    m=QMnFm = \dfrac{QM}{nF}
  • L33
    Lesson 33
    Time to plate
    the full ladder · mass, current or clock in turn

    A plating shop never asks for a mass. It asks for a setting: how many amperes, for how many minutes, to land the thickness the drawing calls for.

    The formulas in this lesson
    m=QMnFm = \dfrac{QM}{nF},Q=ItQ = It
  • ★
    Boss lesson
    The Electroplating Shift
    the boss · no calculator · size the cell, run the current, weigh the rack

    No calculator. F = 96500 C/mol, and every draw is pinned so the coulombs land on a clean fraction of a mole of electrons — 0.300, 0.600, numbers you can carry in your head from one line to the next.

Gases & Solutions

  • L35
    Lesson 35
    The three gas laws
    one knob at a time · Boyle, Charles, Gay-Lussac

    A fixed amount of gas has three knobs: pressure P, how hard it drums on its walls; volume V, the space it is allowed to fill; and temperature T, the average kinetic energy of its molecules.

    The formulas in this lesson
    P1V1=P2V2P_1 V_1 = P_2 V_2,V1T1=V2T2\dfrac{V_1}{T_1} = \dfrac{V_2}{T_2},P1T1=P2T2\dfrac{P_1}{T_1} = \dfrac{P_2}{T_2}
  • L36
    Lesson 36
    Combined and ideal
    several knobs at once · PV = nRT · 22.4 L/mol

    Same fixed amount of gas, same subscript convention (1 before, 2 after), and now any of the three knobs may move. Pin any one of them and the matching pair cancels, handing you Boyle, Charles or Gay-Lussac back.

    The formulas in this lesson
    P1V1T1=P2V2T2\dfrac{P_1 V_1}{T_1} = \dfrac{P_2 V_2}{T_2},PV=nRTPV = nRT,V=n VmV = n\,V_m
  • L37
    Lesson 37
    Molar mass from the gas
    Weigh a litre, name the gas

    Two definitions meet here.

    The formula in this lesson
    ρ=PMRT\rho = \dfrac{PM}{RT}
  • L38
    Lesson 38
    Partial pressures
    Dalton's law · a share of the moles is a share of the pressure

    Ideal gas molecules ignore each other. Put two gases in one vessel and each behaves exactly as if it owned the place, so the pressures simply add — that is Dalton's law of partial pressures.

    The formula in this lesson
    Pi=xi PtotalP_i = x_i\,P_{\text{total}}
  • L39
    Lesson 39
    Graham's race
    lighter is faster — but only by a square root

    Temperature is average kinetic energy.

    The formula in this lesson
    r1r2=M2M1\dfrac{r_1}{r_2} = \sqrt{\dfrac{M_2}{M_1}}
  • L40
    Lesson 40
    Three ways to say how much
    molarity · molality · mass percent

    Three measures, three denominators, and the denominator is the whole story.

    The formulas in this lesson
    C=nVC = \dfrac{n}{V},b=nmsolventb = \dfrac{n}{m_{\text{solvent}}},c=msolutemsolution×100%c = \dfrac{m_{\text{solute}}}{m_{\text{solution}}} \times 100\%
  • L41
    Lesson 41
    Colligative counting
    ΔTb, ΔTf and Π · the solute's identity never matters

    A colligative property depends on HOW MANY solute particles are dissolved and not at all on what they are — the word shares a root with “collect”.

    The formulas in this lesson
    ΔTf=Kf b\Delta T_f = K_f\,b,ΔTb=Kb b\Delta T_b = K_b\,b,Π=MRT\Pi = MRT
  • L42
    Lesson 42
    Vapour pressure stories
    Raoult · Henry · Clausius–Clapeyron

    Above every liquid sits a vapour, and three laws tell you how much.

    The formulas in this lesson
    P=x P0P = x\,P^{0},C=HPC = H P,ln⁡ ⁣(P2P1)=−ΔHvapR(1T2−1T1)\ln\!\left(\dfrac{P_2}{P_1}\right) = -\dfrac{\Delta H_{vap}}{R}\left(\dfrac{1}{T_2} - \dfrac{1}{T_1}\right)
  • ★
    Boss lesson
    The Gas Works
    the boss · no calculator · compress it, mix it, weigh it

    No calculator — every draw is pinned to mental arithmetic, and the standard state does the heavy lifting: at STP one mole fills 22.4 L, and the compressor's pressures and temperatures are whole multiples of 101 kPa and 273 K, so the…

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