I.
Dissociation: the separation of
ions from each other when an ionic compounds dissolves
A.
water will be attracted to and attract the ions that are in the solid
phase
B.
the water pulls the ions apart and into solution; each ion is pulled away from its neighbors
C.
the water molecules surround each ion, called hydration, if the solvent is other than water,
this surrounding process is
called solvation
D.
the number of moles of particles present in the solution is greater than
the number of moles of
formula units in the solid because the
ions in the solid are pulled apart;
each ion in solution acts independently
II.
Precipitation reactions: a
double displacement reaction between ionic compounds where the ions
in solution recombine to form
an insoluble solid – a precipitate (also called metathesis reactions).
III.
Solubility Rules: You must
MEMORIZE THESE!
Salts are written in ionic form if
soluble, and in molecular form if insoluble.
IV. Writing Equations
of the reactants and products in
solution.
electrolytes. All substances that are strong electrolytes
(substances that dissociate or ionize completely, or almost completely, in water) are represented as ions.
ions are not included. Spectator ions are ions that remain
unchanged during the reaction.
compounds,
ions are not present in molecules. They
are formed in the process of dissolving in a polar solvent.
VI.
Strong versus weak electrolytes
VII. Colligative properties - properties that
depend on the number of particles present in solution and
not the type of particles; vapor
pressure, freezing point, boiling point, and osmotic pressure (rate of
diffusion through a semipermeable membrane)
VIII.
Raoult's
Law - the vapor pressure of a solution is directly proportional to the mole
fraction of
solvent present: Psolution = csolvent .
Psolvent
IX.
Vapor pressure
break the attraction forces
and leave the surface to enter the vapor phase
vapor phase
C. the vapor pressure of a solution is lower
than the vapor pressure of the pure solvent
X.
Freezing point
A. the temperature where the vapor pressure of
the solid equals the vapor pressure of the liquid
pressure of the solid equals
the vapor pressure of the liquid is lowered
depression
XI.
Boiling point
A. the temperature where the vapor pressure of
the liquid equals atmospheric pressure
the vapor pressure to
atmospheric pressure
elevation
XII.
Osmotic pressure, ∏
A. the pressure developed across a
semipermeable membrane due to different diffusion rates
B. temperature dependent
XIII.
Amount of freezing point and boiling point change
A. molality of the solution: m - the number of moles of solute per
kilogram of solvent
B. the number of particles in the solution, the
van’t Hoff factor - i
1. nonionizing solutes
a. molecules that do not dissociate, organic compounds do not ionize
b.
the number
of moles of particles present in the solution is the number of moles of
molecules in the solid; 1 mole of solid
sugar = 1 mole of wet sugar in solution
2. ionizing solutes
a. ionic compounds that dissociate into its component ions
b.
the number
of moles of particles present in the solution is dependent upon the number of
ions
in the compound
C. molal constants - kf and kb (TABLE 14-2 page 438)
1.
molal
constants - how much the freezing or boiling point of 1 kilogram of solvent
changes per
molal of nonvolatile solute
particles
2.
the molal
freezing point constant (kf) of water is –1.86 ºC per molal of
particles
3. the molal boiling point constant (kb)
of water is 0.512 ºC per molal of particles
D. ∆FP = m.i.kf and
∆BP = m.i.kb
E. FPsolution = FPsolvent
– ∆FP and the (–) comes from
the (–) on the kf value
BPsolution = BPsolvent
+ ∆BP
XIV.
Amount of osmotic pressure change
A. molarity of the solution: M - the number of moles of solute per Liter
of solution
B. the temperature, in Kelvin (TinK)
C. the gas constant, R = 0.0821 L.atm/mol.K
D. ∏ = MRT
XV.
All intermolecular forces (solute-solute, solute-solvent,
solvent-solvent) are not equal
temperature, called the
activity of an ion
changing the temperature