Bac Séries F Côte d'Ivoire - independent subject practice cheat sheet

v_c = π·D·n/1000, with D in mm and n in rpm

Machining time t = L/(f·n)

Forming conserves mass and produces no chips

Cpk compares both specification distances with three estimated process standard deviations; acceptance requires a stated criterion and a stable suitable model.

Instrument resolution and accuracy depend on the specified device and calibration; they are not fixed by instrument name alone.

Tolerance is a range; fit is the relationship between two tolerances

In an ideal planar model: pin has two force components, roller one normal reaction, fixed support two force components and a moment.

I = b·h³/12, W = b·h²/6 for a rectangle

Simply supported beam, central load: M_max = F·L/4

Euler: P_cr = π²EI/L_k², with L_k depending on the end conditions

Planar DOF: G = 3(n−1) − 2j₁ − j₂

For the defined ideal lossless gear pair, speed and torque-magnitude ratios are inverse; losses reduce actual output torque.

For a sinusoid V_rms = V_peak/√2; the stated impedance magnitude is for a series RLC model.

Q_C = P(tan φ₁ − tan φ₂) for power-factor correction

Transformer: V₁/V₂ = N₁/N₂ = I₂/I₁

Induction motor: n = (1 − s)·60f/p

Thévenin voltage is open-circuit voltage; deactivate independent sources to obtain resistance while preserving dependent-source behavior.

Karnaugh: give the minimum sum of products

Sensitivity = Δoutput/Δinput; resolution = smallest detectable change

Closed-loop error compares reference and measurement; integral action can remove appropriate steady-state error only under suitable stability and operating assumptions.

PLC scan: read inputs → run program → update outputs

4–20 mA live zero: (I − 4)/16 of the span

Repeatability ≠ accuracy, resolution ≠ sensitivity

Robot DOF come from its joints; workspace is the reachable volume

State the system boundary and assumptions before calculation.

Units, sign conventions and uncertainty are part of the answer.

Verification against a specification differs from validation for an intended use.

Drawings need a declared convention and controlled revision.

Classroom models do not authorize physical operation or structural approval.

Chain rule: never drop the inner derivative g'(x).

Integration by parts: choose u so du is simpler than u.

Change limits immediately when substituting in a definite integral.

Improper integrals require an explicit limit, not direct substitution.

Implicit differentiation collects dy/dx terms after differentiating both sides.

State domain restrictions before simplifying; cancelled factors still exclude values.

Composition f(g(x)) is evaluated inside-out and is generally not commutative.

Inverses require one-to-one functions; domain and range swap.

Horizontal transformations act opposite to the sign or factor shown.

Log laws convert sums to products, enabling solution of log equations.

Always check candidate solutions against original domain restrictions.

Resolve vectors before applying F = ma or the SUVAT equations

Momentum is a vector: conserve each component only when the corresponding net external impulse is zero

Equilibrium requires both zero resultant force and zero resultant moment

The centripetal component points to the centre; uniform circular motion has constant speed but changing velocity

SHM signature: a = −ω²x, giving T = 2π/ω

State g and sign conventions explicitly at the start of a solution

EMF is per unit charge from the source; terminal p.d. is E − Ir

Kirchhoff's laws follow from conservation of charge and energy

Capacitor energy is ½CV²; discharge is exponential with time constant RC

Magnetic-force magnitude is |q|vB sinθ and its vector is perpendicular to velocity, so magnetic force does no work

n = m/M, n = cV (V in dm3) and n = V/24.0 for gases at RTP are the three key conversions.

The limiting reagent is the one with the smallest moles ÷ coefficient; product amount depends on it.

Percentage yield measures practical success; atom economy measures how much reactant mass is useful.

Dilution uses c1V1 = c2V2 because the moles of solute do not change.

Always balance the equation before applying any molar ratio.

ΔH is negative for exothermic reactions; standard enthalpy of formation of an element in its standard state is zero.

q = mcΔT uses the total mass of solution, and ΔH per mole = −q/n.

Hess's law lets you combine any route; combustion data are used in the reverse order to formation data.

ΔH = Σ bonds broken − Σ bonds formed, and mean bond enthalpies are averages.

Feasibility is determined by ΔG = ΔH − TΔS, not by ΔH alone.

Orders are determined experimentally, not from stoichiometric coefficients.

Rate constant units depend on overall order: for second order overall, dm3 mol−1 s−1; for third order overall, dm6 mol−2 s−1.