Bac Sciences Expérimentales Algeria - independent subject practice cheat sheet

Prokaryotes lack a membrane-bound nucleus; bacterial peptidoglycan walls are not universal and archaeal walls differ.

Fluid mosaic membranes contain a lipid bilayer and proteins; sterol and carbohydrate composition depends on the cell.

Facilitated diffusion is passive; primary active transport may use ATP directly and secondary transport uses a gradient.

Water potential ψ = ψs + ψp; water moves from higher (less negative) to lower ψ.

Mitosis (P-M-A-T) after S-phase replication maintains chromosome number.

Cytokinesis: cleavage furrow in animals, cell plate in plants.

Condensation forms glycosidic, ester and peptide bonds; hydrolysis reverses them.

Reducing-sugar test interpretation requires suitable assay conditions and controls; hydrolysis can change sucrose test results.

Cellulose = β-1,4 glucose, straight H-bonded microfibrils; starch and glycogen = α-glucose.

Triglyceride = glycerol + 3 fatty acids; phospholipid = phosphate head + 2 tails, amphipathic.

Negative feedback reverses a deviation; positive feedback amplifies and must terminate.

Surface area to volume ratio drives the need for specialized exchange surfaces.

Pulmonary arteries carry deoxygenated blood away from the heart.

Xylem moves water up (cohesion–tension); phloem moves sugars by pressure flow.

Insulin lowers blood glucose; glucagon raises it - both are negative feedback.

Los virus son acelulares; los ciclos lítico y lisogénico son modelos de determinados bacteriófagos, no de todos los virus.

Retrovirus: retrotranscriptasa convierte ARN en ADN e integra el provirus.

Muchas bacterias tienen peptidoglicano; pared, plásmidos y otros rasgos deben comprobarse en cada organismo.

Linfocitos B → células plasmáticas → anticuerpos; CD4 ayudan y CD8 citotóxicos matan células infectadas.

La memoria adaptativa puede acelerar la respuesta; el predominio de IgG depende del contexto de la respuesta sistémica.

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.

Relative atomic mass is an abundance-weighted mean of isotope masses, calculated from mass-spectrum data.

Across a period effective nuclear charge rises, so radius falls and ionisation energy and electronegativity rise.

Large jumps in successive ionisation energies reveal the number of electrons in the outer shell.

Cr and Cu adopt 3d5 4s1 and 3d10 4s1 configurations; 4s electrons are removed first on ionisation.

Transition metals require a partially filled d subshell in at least one common oxidation state.

VSEPR: count all electron domains, then apply lone pair–lone pair > lone pair–bond pair > bond pair–bond pair repulsion.

Molecular polarity requires both polar bonds and an asymmetric arrangement of those bonds.

Higher bond order gives a shorter, stronger bond; resonance spreads the order over equivalent positions.

Only period 3 elements and below can expand their octet; N, O, F and C cannot.

Ionic lattice strength increases with ion charge and decreases with ion radius.

Convert to K and m3 before using PV = nRT; R = 8.314 J mol−1 K−1.

Real gases deviate from ideality at high pressure and low temperature.

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

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.

S-waves cannot pass liquids, revealing a liquid outer core

Divergent, convergent, and transform boundaries produce distinct features

Cross-cutting relationships and superposition establish relative ages

Igneous (intrusive vs extrusive), sedimentary, and metamorphic rocks cycle

Atmosphere: 78% N2, 21% O2; weather occurs in the troposphere

End-Cretaceous extinction linked to asteroid impact and iridium layer

State resolution and uncertainty convention for each instrument

Random errors → repeats and means; systematic errors → correction

For first-order worst-case bounds, add relative contributions; independent standard uncertainties use quadrature

Gradient from two points on the best-fit line, with units

Average repeated timings and time many oscillations to cut reaction error

Never quote more significant figures than the data justify