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Q: What determines the choice of separation method?
A: The difference in physical properties between components (e.g., boiling point, solubility, adsorption, magnetism, density).
Q: Define solvation.
A: Process where solvent particles surround & attract solute particles, allowing dissolution; in water it’s called hydration.
Q: Why is solvent choice critical for separations?
A: It must dissolve the target but not the others, enabling selective removal (e.g., salt dissolves in water; sand doesn’t).
Q: Steps: separate salt + sand.
A: Add water → stir → filter (sand = residue, salt solution = filtrate) → evaporate water → collect salt.
Q: Define filtration.
A: Separation of insoluble solid from liquid/solution using filter paper (filtrate passes; residue remains).
Q: When to use vacuum filtration?
A: For fine/compact solids or when gravity filtration is slow—uses reduced pressure to speed collection.
Q: When to use centrifugation?
A: To separate tiny or dense particles from liquid when filtration is ineffective; separation by density under rotation.
Q: Define crystallisation (crystallization).
A: Recovery of a dissolved solid by evaporating solvent and cooling so solubility decreases and crystals form.
Q: Key steps in crystallisation.
A: Gently heat to concentrate → cool to saturation → seed/test on cold rod → cool slowly → filter, wash, dry.
Q: Two critical cautions in crystallisation.
A: Don’t boil to dryness; and cool slowly for larger, purer crystals.
Q: Define recrystallisation.
A: Purifying an impure solid: dissolve in minimum hot solvent, remove insoluble impurities (hot filtration), cool slowly to crystallise, vacuum filter, wash cold solvent, dry.
Q: Why “minimum hot solvent” in recrystallisation?
A: Minimizes product loss; ensures target recrystallises upon cooling.
Q: Why wash crystals with cold solvent?
A: To remove soluble impurities without redissolving the product.
Q: Define simple distillation.
A: Separation of a solvent from solute or liquid with a much lower bp than others; vapor → condenser → distillate.
Q: When is fractional distillation required?
A: For miscible liquids with similar boiling points (e.g., ethanol 78 °C vs water 100 °C).
Q: Purpose of the fractionating column.
A: Provides repeated vaporization–condensation cycles (theoretical plates) for better separation.
Q: Safety: heating with flammable liquids.
A: Use an electric heater (not open flame) to avoid ignition.
Q: Define paper chromatography (paper TLC conceptually).
A: Separates dissolved substances by differential solubility in the mobile phase and adsorption to the stationary phase (paper).
Q: Why mark the baseline with pencil?
A: Graphite does not dissolve or migrate; ink would smear and contaminate the chromatogram.
Q: Why must sample spots be above solvent level initially?
A: Prevents dissolving into the reservoir; forces capillary rise to carry analytes up the paper.
Q: What makes a spot travel further in paper chromatography?
A: Higher solubility in the mobile phase and weaker adsorption to the paper.
Q: What makes a spot move less?
A: Stronger adsorption to paper and lower solubility in the solvent.
Q: (Extension) Define R_f value.
A: R_f = “distance solute travels/distance solvent front travels” (0–1). Characteristic in given conditions.
Q: Example mapping: air separation method + property.
A: Fractional distillation of liquefied air; components have different boiling points.
Q: Example mapping: food dyes method + property.
A: Chromatography; dyes differ in solubility/adsorption.
Q: Example mapping: iron + sulfur method + property.
A: Magnetic separation; iron is ferromagnetic, sulfur is not.
Q: Quick diagnostic: mixture vs compound in a particle diagram.
A: Mixture: varied, unbonded particles intermingled. Compound: identical bonded units in fixed ratio.
Q: After solvation, why filter?
A: To remove undissolved solids (residue) and collect solution (filtrate) for further steps.
Q: Order of operations: dissolve → filter → crystallise vs filter → dissolve → crystallise?
A: Dissolve → filter → crystallise is correct; filtration works after selective dissolution.
Q: Column choice: simple or fractional for 78 °C ethanol + 100 °C water?
A: Fractional (close bps), heat to ~78 °C first to collect ethanol.