10 - Acids And Bases Flashcards
Arrhenius acids and bases
Defined by dissolution in water to excess of H+ or OH-
Bronstead-Lowry acids and bases
Defined by donation or reception of H+
Lewis acids and bases
- defined by donation or reception of electron pairs
- acids accept electron pair
Amphoteric species
- reacts like acid in basic environment and vice versa
- amphiprotic may behave as BL acid or base: water and polyvalent species
Consistency of equilibrium constants
- only temperature dependent
- otherwise 100% constant
Log and other mathematical properties
Log1=0 Log10=1 Log100=2 Log1000=3 Logxy=logx+logy -log(n x 10^-m)=(-logn)-log(10^-m)=m-logn=m-0.n
(because n is between 1 and 10, -logn will be between 0 and 1)
(6x10^-3)^2 = 36x10^-6
Water dissociation constant and K of WA and WB
Kw [water disossiation constant] =[H3O+][OH-]=10^-14
- weak acids defined by Ka less than 1
- weak bases defined by Kb less than 1
- conjugate of a strong acid of base is inert
Hydrolysis and neutralization reactions
- hydrolysis: salt ions react with water to give back acid and base
- neutralization reactions form salt and sometimes water
Titrations
- oft carried out between acids/bases or oxidation/reduction pairs
- titrant (known [] and volumes) added to titrand (known volume, unknown [])
- WAWB titrations rarely performed
equivalence points
- for SASB titration, equivalence point will be at 7 but that isn’t always the case: otherwise, leans toward stronger of reactants
- equivalence point may be observed by use of an indicator
- equivalence point generally has steepest point on curve for any titration
SASB titrations
Flat- vertical - flat
WA (titrand) SB (titrant)
- more gradual initial curve, vertical, flat
- starting point is farther from zero than SASB
- SA (titrant) and WB (titrand) is inverse
Polyvalent titration curve
- equivalence points at steep segments
- half equivalence points (corresponding to pka values) between equivalence points at flat segments
Buffers
- generally composed of WAWB conjugate pair
- big flat parts of curve
- greatest buffering capacity is about 1pH range within pKa of acid of buffer
Henderson-Hasselbalch
- pH=pKa+log[A-][HA]
- greater [], same ratio increase buffering capacity - less of a pH change with addition of A or B
- use normality / equivalence equation to get []: N1V1=N2V2
- optimal buffering occurs when pH = pKa