Acids and Bases Flashcards
What do all acids release
H+
What do all bases accept
H+
Common bases
Metal oxides
Metal hydroxides
Ammonia and amines
Alkalis (soluble bases that dissolve in water release in water
OH- ions
How are salts made
When H+ from acid is replaced by a metal ion/another positive ion
Neutralisation reactions
Acids react with: carbonates to form CO2 bases (metal oxides) to form H2O alkalis to form H2O Metals to form H
Redox reactions
Acids react with metals
Metal is oxidised
Hydrogen is reduced
Ammonia
Forms weak alkaline solution when dissolved in H2O
Salt crystals features
Have water = crystalline form, hydrated
No water = powdered form, anhydrous
Molar proportion of H2O 名前 water of crystallisation
Hydrated salt formula
1: calculate n of anhydrous
2: calculate n of H2O
3: determine hydrated salt ormula
Titration calculation method
1) find n of compound in the sol
2) use equation to ID mol no. of substances in 2nd sol.
3) ID n for any other relevant substances
4) scale quantities to match
5) calculate M
Bronsted-Lowry model
(conjugate) Acid = H+ donor
(conjugate) Base = H+ acceptor
Alkali = base that dissolves in H2O forming OH-
Water’s acid-base equilibrium
Ha(aq) ⇌ H+(aq) + A-(aq)
Acid strength
Extent to which it dissociates into H+ and A-
Strong acid strength
Almost complete dissociation
Weak acid strength
Partial dissociation
Equilibrium favours non-dissociated side
Ka, acid dissociation constant
Dissociated side/non-dissociated side
Unit = mol dm-3
Large vs small Ka
Large Ka = large dissociation, strong acid
Small Ka = small dissociation, weak acid
Concentration vs strength of acid
Concentration = amount of acid dissolved in 1dm3 o solution
Strength=dissociation extent
pH formula
pH=-log10 [H+(aq)]
H+ formula
[H+(aq)]= 10-pH
pH value meanings
Low H+ value = high pH value
High H+ value = low pH value
pH changed by 1 =
H+ changed by 10x
Strong acid pH calculations
Found directly from acid concentration
[H+]=[HA]
Weak acids pH calculation
Need acid concentration and Ka value
Consider:
[HA(aq)]equilibrium ≈ [HA(aq)]start
[H+(aq)] ≈ [A-(aq)]
Formula therefore:
Ka ≈ [H+(aq)]2/[HA(aq)]
pKa and Ka link
Logarithmic version of Ka
pKa = -log10Ka Ka = 10-pKa
Low Ka = high pKa
High Ka = low pKa
Kw
Ionic product of water
Kw=[H+(aq)][OH-(aq)]
Kw at 25 degrees
Kw=1.0x10-14 mol2 dm-6
H+ and OH- in water
Same concentrations,
10-7 mol dm-3. Total therefore:
10-14 mol dm-3
H+ vs OH- concentrations
Water: H+ = OH-
Acid: H+ > OH-
Alkaline: H+ < OH-
Linked by Kw
Strong alkalis pH calculation
1) Find concentration directly from alkali concentration
2) solve for H+ ( Kw/OH-)
3) calculate pH
Titration curve features
Mid-point of vertical bit is Equivalence Point
Indicator is only suitable if its pKind value is within the pH range of the vertical part
Ka from a titration curve
1) Get vol. of alkali for neutralisation from titearion curve
2) get pH at half-neutralisation fron curve
3) half-neut, HA = A-, so Ka = H+
Ka = 10-pH
∆Hneut value
Approximately -57.9kJ mol -1 for strong acids
Less exothermic for weak acids
Buffer soluions
Minimise pH changes by removing most of added acid/alkali
Made of HA and its conjugate base
Adding H+ to a buffer
H+ is increased
pH change is opposed. Equilib moves left removing H+ and forming HA
A- removes most of added H+
Adding alkali to buffer
Added OH- reacts with small concentration of H+
pH change opposed by moving equil to the right, restoring H+ as HA dissociates
HA restores most of lost H+
Buffer solution pH depends on
- Ka of buffer system
* ratio of weak acid and its conjugate base
Arrhenius acids and bases
Acids: dissociate in water to make H3O+
Bases: dissociate to make OH-
Lewis acids and bases
Acid aka electrophile: e- acceptor
Base aka nucleophile: e- donator
Acid-conjugate base link
Acids are directly proportional to conjugate base’s stability.
More stable = more acidic
Base stability considerations
Larger atoms いい More electronegative いい sp hybridised >sp2>sp3 いい e- withdrawing groups on acid いい Resonance structures いい
pKa values
V strong acids = pKa &<0
Weak acids = pKa 0-9
Equilibrium rule
Equilibrium of a reaction will favour side with weaker acids and bases
Acid dissociation constant
Ka = [H+][A-]/[HA]
Buffer solution pH
pKa + log10 (salt/acid)