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How to Predict whether a salt solution will be acidic basic, or neutral practice question 30 on page 100 ka=kw/kb
How to Predict whether a salt solution will be acidic basic, or neutral practice question 30 on page 100
Monoprotic acids: vice versa with bases
1 h+ can be donated
Diprotic acids vice versa with bases
2 h+ can be donated over the course of 3 ionizations
Triprotic acids vice versa with bases
3 h+ can be donated over the course of 3 ionizations
What defines a buffer & why are buffers useful?
Consists of an acid and its conjugate base OR a base and its conjugate acid. Buffers help maintain pH (prevent large pH changes when acid/base is added to a solution)
Calculate the pH of a buffer before and after addition of acid/base pH=pKa + log(b/a)
Before: Use the relevant Henderson-Hasselbalch Equation
After: Assume the strong acid/base reacts completely with the weak base/acid. Then use the Henderson-Hasselbalch Equation.
a solution containing appreciable (good) amounts of an acid-base conjugate pair
Buffer
What have we learned about buffered vs. unbuffered solutions
prevent drastic changes in pH!
Can buffers maintain the pH of a solution indefinitely
no
amount of acid or base that can be added to a given volume of buffer solution before the pH changes significantly (by ≥ 1 pH unit)
buffer capacity
the greater the concentration of acid/conjugate base (or base/conjugate acid), the
greater the buffering capacity of the solution.
Rules for picking a good buffer:
Aim for equal concentrations of each component
Choose a system with a pKa near your desired pH
Interpret titration curves for strong and weak acid-base systems
What is the nature of the unknown solution—is it a weak acid or a weak base? How do you know? What’s the approximate Kb of the base? How do you know? What is the nature of the titrant? How do you know?
Calculate solution pH at different points in a titration & use titration data to calculate the concentration of an unknown solution
See worked example here & CoursePak #22-24 (p. 114-115) Calculate solution pH at different points in a titration
What is the purpose of acid-base indicators?
To detect pH changes; visualize equivalence points/end points in titrations
plot of some solution property as a function of amount of titrant added (usually a plot of pH vs. volume of strong acid or base added)
titration curve
equal amount of acid and base present (stoichiometric amounts of acid/base reacted)
Equivalence point
Why does this part of the curve flatten a bit (have its own inflection point)?
Here it acts as a buffer!
What’s the point of doing a titration
can be used to quantify acid/base concentrations in solution
Manual titration: Remember: at the equivalence point (visualized as the “ending point” or “end point”)
the amount of acid and base present are equal.
substances (weak organic acids or weak organic bases) used to determine the pH of a solution (via visual color change)
acid-base indicators
Write chemical equations & equilibrium constant expressions (Ksp) for solubility equilibria
See worked examples here (remember not to include solids!) Write chemical equations & equilibrium consta
Determine the molar solubility or Ksp for a compound
See worked examples here (write equations, Ksp expressions, and use ICE charts) Determine the molar solubility
Predict whether a precipitate will form given specified concentrations of aqueous ions (and Ksp values for the corresponding solid(s)
Calculate Qsp and compare it to Ksp (if Qsp < Ksp Ă no precipitation; if Qsp > Ksp Ă precipitation
Explain how common ions and solution pH affect ionic compound solubility in aqueous solution
Effects on solubility determined by how other ions in solution alter solid-derived dissolved ion levels (equilibria shifts according to Le Chatelier’s Principle)
*Remember: Q is found using the same expression as K
but at unknown or non-equilibrium conditions
If Q < K, in which direction will the reaction proceed?
forward
If Q > K, in which direction will the reaction proceed?
reverse
If Qsp < Ksp, the compound will
dissolve (stay in solution)
If Qsp > Ksp, the compound will
precipitate
Forward =
Dissolve (stay in solution)
Reverse =
precipitate
Compounds that dissociate to give weak base ions
dissolve better in acidic solutions.
Compounds that dissociate to give weak acid ions
dissolve better in basic solutions
Solids that produce basic anions will become
more soluble at low pH
Metal hydroxide solubility decreases in basic solutions where
Hydroxide concentrations are high
Solids that produce acidic anion are more
soluble in basic solutions
In buffer FRQ look for
find Ph of before addition of strong acid or base. Use H.H equation. You can use mol or Molarity in division but remember to add new mL amount
Percent ionization also is called
percent dissociation
percent ionization equation for acids
H30+ (AT EQUALIBRIUM) // HA (INITIAL) X 100
percent ionization equation for bases
OH- (AT EQUALIBRIUM) /// B (INITIAL) X 100
Id you see a FRQ asking for Ka of a weak acid or base first
Set up ice chart ***at equalibrium assume x is too small and disregard
In saturated solution FRQ Separate the solid into its
ions. Ksp = new ionic side without solid side! Stochiometric goes in exponent in the KSP expression
What do you always forget
SIGFIGS!!!!!!!!
When adding a product equilibrium will shift
in reverse to counter added product
If adding sodium to a solution
no change will be made
If you see a titration FRQ
M1*V1=M2*V2 remember to stay consistent with mL or L
Equation for molar mass
g/mol
equation for mols
L*M
Equation for Molarity
mol/L
pH = -log(M concentration)
pOH = -log(M concentration)
14 - pH = pOH
14 - pOH = pH