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K_sp
used to measure the the dissolution of an ionic compound
molar solubility (S)
unit: mol/L
change in S_universe can be used to prove spontaneity when it’s…
greater than 0 (positive)
solubility and pH
if pH is high, then [OH] is high and equil shifts left
if pH is low, then [H3O] is high and equil shifts right
hydroxides, sulfides, and carbonates are more soluble in…
acidic water
how does a precipitate form?
when a solution has 2 ionic compounds and one is insoluble
Q and K_sp
if Q < K_sp, reaction goes right, solution is unsaturated, and more solid can be added
if Q = K_sp, reaction goes right, solution is saturated, and equil is reached
if Q > K_sp, reaction goes left, solution is supersaturated, and rhe excess solid precipitates
ligand
neutral molecule/ion that acts as a lewis base with a central ion
complex ion
has a central metal ion bound to 1 or more ligands
when K_f is large, what happens
equil will favor the product and most of the reactant will be used up. in those cases we can use that inital conc as the variable
spontaneous process
can a reaction happen on its own
in thermodynamics, we consider the direction and extent of the reaction
in kinetics, we consider the speed of the reaction
increases with entropy
how can a nonspontaneous process become spontaneous?
by coupling it with a spontaneous process OR getting energy from another source
entropy
increases with the number of ways (W) to rearrange components
increases with spontaneity
unit: J/K
macrostate
overall state of a system defined by given conditions
remains constant
microstate (W)
number of ways to rearrange components
whats the rank of increasing entropy
solid » liquid » gas
that’s because each state is more disorderly than the last
reversible process
happens at melting/boiling point
any tiny change can turn it back
sublimation
solid » gas
condensation
gas » liquid
how do you determine entropy from systems graph
the more levels it has, the more entropy
because that means there is more than 1 way to disperse
ranking entropy (S)
check states
if states are constant check the complexity
if complexity is the same, check mols
if mols are similar on both sides, check molar mass
system entropy vs surrounding entropy
if S_surr increases by a big amount, S_sys can decrease
if S_surr is positive, it’s spontaneous under low temps
if S_sys is positive, it’s spontaneous under high temps
exothermic process
energy disperses into surroundings and entropy increases
endothermic process
energy leaves surroundings and entropy decreases
gibbs free energy (G)
energy available to do useful work
when it’s spontaneous, change in G is negative
when it’s nonspontaneous, change in G is positive
at equilibrium, change in G = 0
change in G vs change in G(degree)
change in G refers to given conditions
change in G(degree) refers to standard conditions
change in G
if Q is very small, then RT*ln(Q) will be a large negative
if Q is very large, then RT*ln(Q) will be positive
change in G(degree) and K
if change in G(degree) is negative, then K > 1 (large)
if change in G(degree) is positive, then K < 1 (small)
if change in G(degree) = 0, then K = 1
oxidation-reduction reactions
aka redox reactions
reactions that create electricity
oxidation
increase in oxidation state (when more electrons are lost in the products)
reduction
decrease in oxidation state (when there’s more gain in electrons in the products)
voltaic cell
a device that uses a spontaneous chemical reaction to make electricity
forces it through a wire
anode
electron where oxidation happens
has a negative charge in voltaic cell
electrons leave from here
cathode
where reduction happens
electrons arrive here
salt bridge
tube filled with electrolytes
neutralizes charge buildup by letting ions flow
without it, reaction stops instantly
cell potentional (E_cell)
unit: volts (V)
the “push” behind electrons
if E_cell is positive, reaction is spontaneous
if E_cell is negative, reaction is nonspontaneous