Q.State and explain Raoult's law for
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Start your 14-day free trial to unlock the full solution →Raoult's law relates vapour pressure to mole fraction — for volatile solutes each component contributes ; for a non-volatile solute, only the solvent contributes, and the fractional vapour-pressure lowering equals the solute's mole fraction.
- Raoult's law for a solution of two volatile liquids: For a solution formed by mixing two volatile liquids 1 (solvent) and 2 (solute), the partial vapour pressure of each component in the solution is directly proportional to its mole fraction: where are the vapour pressures of the pure components. By Dalton's law, the total vapour pressure of the solution is:
- Raoult's law for a solution of a non-volatile solute in a volatile solvent: Here only the solvent (1) contributes to the vapour pressure (the non-volatile solute (2) does not evaporate): Since , i.e. : This relative lowering of vapour pressure of the solvent equals the mole fraction of the (non-volatile) solute — this is the more commonly quoted statement of Raoult's law for such solutions.
OR: Colligative properties, osmosis and osmotic pressure
Colligative properties are properties of a solution that depend only on the number of solute particles present, not on their chemical identity/nature. The four colligative properties are: relative lowering of vapour pressure, elevation of boiling point, depression of freezing point, and osmotic pressure.
Osmosis: the spontaneous flow/movement of solvent molecules from a region of pure solvent (or a dilute solution) into a region of concentrated solution, through a semipermeable membrane (a membrane that allows only solvent molecules to pass, not solute particles). It occurs because the chemical potential (escaping tendency) of the solvent is higher on the pure-solvent side.
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