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specific concentration
quantity of SOLUTE dissolved in a given quantity of solution (or solvent)
aqueous solution
solutions of solute in water (solvent)
concentration
intensive property
measured by molarity (M)
moles of solute per liter of solution
dilution
A concentrated solution is converted to dilute solution by adding solvent
solubility
the amount of substance that can be dissolved in a given quantity of solvent at a specified temperature
insoluble (less than 0.01 mol/L)
polarity
created in water molecule through its uneven distribution of electron charge and bent m/c shape
electrical conductivity
flow of electric current
increases when ionic compounds dissolve
electrolytes
substances whose aqueous solutions conduct electricity (most contain ions)
strong: soluble compounds that completely ionize in water
weak: m/c compounds for which only a small fraction of m/c are ionized in water
nonelectrolytes
substances whose aqueous solutions do not conduct electricity (contains negligible amount of ions)
most molecular compounds
precipitation reaction
2 soluble ionic compounds react to form an insoluble product (precipitate)
key event: formation of an insoluble product through net removal of ions (m/c eq => net ionic eq)
molecular equation
shows all reactants and products as if they were intact, undissociated compounds
total ionic equation
shows all the soluble ionic substances as they actually exist (dissociated ions)
net ionic equation
spectator ions are excluded and only shows the chemical change
metathesis reaction
double displacement reaction
ex) precipitation and acid-base
acids
Arrhenius: substances that in aqueous solutions produce hydrogen ions (H+)
For now: m/c substances that IONIZE in aqueous solutions, releasing hydrogen ions (H+ = proton)
PROTON DONORS
strong acids
acids that ionize completely in an aqueous solutions (→)
H2SO4, HI, HBr, HNO3, HCl, HClO4
(SO I Brought NO Clean ClOthes)
weak acids
acids for which only a small fraction of m/c are ionized (⇌)
HF, H3PO4, CH3COOH
polyprotic acid
ionization is represented in stages
base
Arrhen: substances that produce OH- ions when dissolved in water
proton acceptors
strong base
completely dissociates into ions in an aq solution
group 1 hydroxides
Sr Cat Bad (Sr, Ca, Ba)
weak bases
partially ionize in aqueous solution
ammonia (NH3)
titration
known concentration of one solution is used to determine the unknown concentration of another
standard solution
concentration is known
equivalence point
amount of H+ ions in the original volume of acid has reacted with SAME amount of OH- ions from buret
moles of H+ and OH- are stoichiometrically equal
end point
point at which indicator changes colour (tiny excess of OH- ions changes colour)
in calculations this excess is insignificant
oxidation reduction reactions
net movement of e- from one reactant (with less attractions for e-) to the reactant with MORE attraction for e-
Ionic compounds TRANSFER e-
Covalent compounds SHIFT e-
oxidation
loss of electrons
reducing agent is oxidized (loses electrons)
reduction
gain of electrons
oxidizing agent is reduced (gains electrons)
types of redox reactions
combination (X+Y→Z)
decomposition (Z→X+Y)
single displacement (X+YZ→XZ+Y)
combustion
activity series of metals
metals are ranked by their ability to displace H2
any metal can displace (reduce) the ions of metals BELOW it
single displacement won’t occur if metal is trying to displace ions of metal below it
pressure
force of collisions with walls
force exerted per unit of surface area (F/A)
barometer
measures atmospheric pressure
tube filled with Hg is inverted into a dish and vacuum forms above Hg
PHg = Patm
closed end manometer
Hg filled curved tube closed on one end and attached to flask at the other
∆h = Pgas
open end manometer
Hg filled curved tube is open at one end and attached to a flask at the other
∆h = difference between Pgas and Patm
ideal gas
gas that exhibits linear relationships among volume, pressure, temperature, and amount
described by gas laws
Boyles law
V∝1/P at constant temperature
P1V1=P2V2
Charles law
V∝T at constant pressure
V1/T1 = V2/T2
avogadros law
V∝n at fixed pressure and temperature
V1/n1 = V2/n2
STP conditions
1 atm and 273.15K
Kinetic molecular theory
negligible volume of particles compared to whole sample (point mass)
negligible force
elastic collisions
Average KE of particles is proportional to absolute
maxwell boltzman distribution
most probable speed increases with temperature
temperature
a measure of the average KE of a particle
root mean square speed
a particle moving at this speed has average KE
real gases
gas particles are NOT point mass with 0 volume
Attractive and repulsive forces DO exist
strong acid and strong base
Net ionic: H++ OH- → H2O
weak acid and strong base
intact acid m/c on reactant side for net ionic
cation of strong base is spectator
ex) CH3COOH + OH- → H2O + CH3COO-
insoluble base and strong acid
Intact base on reactant side for net ionic
ex) net: Mg(OH)2 + 2H+ → 2H2O + Mg2+