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Acids & Bases typically are, or behave as, IONIC compounds.
• Acids:• Are corrosive• Taste sour• React with
indicators• Neutralize bases
• Ex.
HCl (hydrochloric acid), H2SO4 (sulfuric acid)
Bases: Are slippery Taste bitter React with indicators Neutralize acidsEx.
NaOH (sodium hydroxide),
NH4OH (ammonium hydroxide)
Baking soda (NaHCO3)
Litmus is a vegetable dye obtained from certain lichens found principally in the Netherlands.
The difference between the aqueous solution processes of ionization and dissociation.
Typical with Acids Typical with Bases
NomenclatureAcids Most are
“hydrogen” bonded with an anion
Examples: HNO3 (nitric acid)
HC2H3O2 (acetic acid)
HCl (hydrochloric acid)
Bases Most are metal
hydroxidesExamples: NaOH (sodium hydroxide)
KOH (potassium hydroxide)
Ba(OH)2 (barium hydroxide)
NH4OH* (ammonium
hydroxide)
Definitions
AcidsArrhenius - acids donate H+ (in soln)
Bronsted-Lowery -acids donate H+ (in soln)
BasesArrhenius - bases donate OH- (in soln)
Bronsted-Lowery - bases accept H+ (in soln)
Coordinate covalent bond
Conjugate Acid-Base Pairs
The transfer of protons illustrates the characteristics of conjugate pairsHNO2 + H2O <==> H3O+ + NO2
-
NO2- is the conjugate base of HNO2
H3O+ is the conjugate acid of H2O
Protocity
Monoprotic HCl, HNO3
Diprotic H2CO3
Triprotic H3PO4
Acids can be classified according to the number of hydrogen ions (protons) they can transfer per molecule during an acid-base reaction.
Acid-Base Strength(You can dilute an acid or a base but you can’t change its strength)
Strong
“ions” completely dissociate in water
ACIDS:
HCl, HBr, HI,
HClO4, H2SO4, HNO3
BASES:
LiOH, NaOH, KOH,
Ca(OH)2, Sr(OH)2, Ba(OH)2
Weak “ions” partially
dissociate in waterAll non-strong acids & basesThese exist as equilibrium systems in solution, thus, their “weakness” exists within a range defined by their Keq values.
A comparison of the number of acidic species present in strong acid and weak acid solutions of the same concentration.
Weak A/B equilibrium
Two reactions (forward & reverse) occur at the same rate
HA <==>H+ + A-
BOH <=> B+ + OH-
Equilibrium expressions are ways to show the mathematical relationships
Keq = [Products]n
[Reactants]m
n & m are the coefficients of each substance
Ionization Constants for Acids & Bases
HA(aq) + H2O(l) <==> H3O+(aq) + A-(aq)
Ka = ---------------------
B(aq) + H2O(l) <==> BH+(aq) + OH-(aq)
Kb = ---------------------
Neutralization reactions- a special type of DR rxn
AX + BY --> AY + BX
HCl + KOH --> HOH + KCl
Acid + Base --> Water + Salt
To balance these rxns. Balance the H in the acid with the OH in the base :)!For a complete reaction, stoichiometric equivalents of the acid and base must be used.
Neutralization equations
HCl(aq) + NaOH(aq) --> H2O(l) + NaCl(aq)
H2SO4 + Ba(OH)2 -->
H3PO4 + KOH -->
HNO3 + Al(OH)3 -->
The acid-base reaction between sulfuric acid and barium hydroxide produces the insoluble salt barium sulfate.
Calculations
A sample of 0.0084 mol HCl is dissolved in water to make 1500 mL solution. Calculate the molarity of the HCl solution and the [H3O+].
Self-Ionization of Water (pH is a derivative of this concept)
Water molecules can break apart when they collide
H2O(l) <==> H+(aq) + OH-(aq)
Kw = ----------------
Kw = 1.0 x 10-14 M2
Adding an acid or a base changes the relative amounts of [H+] and [OH-] but not the value of Kw.
Ionic ConcentrationIf [H+] = [OH-] the solution is neutral
If [H+] > [OH-] the solution is acidic
If [H+] < [OH-] the solution is basic
[H+] x [OH-] = 1.0 x 10-14M2
The relationship between H3O+ and OH- in aqueous solution is an inverse proportion.
pH: a logarithmic scale of a solution’s hydrogen (hydronium) ion concentration (molarity)
This is a way to express the relative acidity/basicity of a solution.
pH = -log[H+] Therefore, each difference in pH of 1.0 is
equivalent to a concentration change by a factor of 10
High [H+] causes low pH Low [H+] causes high pH Therefore, strong acids have lower pH!
pOH = -log[OH-]
Calculations
If the [H+] = 3.35 x 10-5 M, what is the pH of the solution? On your calculator:
- log (3.35 x 10-5) =
pH --> [H+] calculations
What is the [H+] for a solution with a pH = 3.92?pH = -log[H+]
3.92 = -log[H+]
-3.92 =log[H+]
10-3.92= [H+]
[H+] = 1.20 x 10-4M
Practice: determine the [H+] for the solutions with the following values.
[H+] = 2.82 x 10-8 M
[H+] = 3.98 x 10-11 M
[H+] = 7.86 x 10-3 M
[H+] = 3.16 x 10-10 M
pH = 7.55
pH = 10.4
pH = 2.12
pOH = 4.5
Salt HydrolysisSome aqueous salt solutions have the ability to split (hydrolyze) water and form compounds which result in larger [H+] or [OH-] in the solution.Example: Aluminum chloride
AlCl3(aq) --> Al+3(aq) + 3Cl-(aq) Cation of WB Anion of WA
Aluminum ion will react with OH- in solution: Remember: H2O <==> H+ + OH-
Al+3(aq) + H2O(l) <==> Al(OH)3(aq) + 3H+(aq) Chloride ion will NOT react with H+ in solution!
Rules for Determining pHStrength wins!
Strong Acid + Strong Base --> Neutral sol’n HCl + NaOH --> NaCl + H2O
Strong Acid + Weak Base --> Acidic sol’n HCl + Al(OH)3 --> AlCl3 + H2O
Weak Acid + Strong Base --> Basic sol’n H2S + NaOH --> Na2S + H2O
Weak Acid + Weak Base --> depends on the salt
HNO2 + NH4OH --> NH4NO2 + H2O
BuffersBuffers are solutions in which the pH remains relatively constant when small amounts of acid or base are added
Two active chemical species: A substance to react with & remove added base A substance to react with & remove added acid.
Buffers are solutions of a weak acid and one of its conjugate base OR a weak base and one of its conjugate base.
Buffering Action in Human Blood
H2CO3 <==> H+ + HCO3-
High concentration High concentration
Ratio: 1 : 10Add a base [OH-] and the equilibrium position shifts ; pH doesn’t change muchAdd an acid [H+] and the equilibrium position shifts ; pH doesn’t change muchReason: high [ ] of acid and anion can accommodate large shifts of EQ position.Lots of acid is
produced in the body
daily.
Titration
At the completion of a neutralization reaction (equivalence point) the
# moles acid = # moles base
So,
MaVa = MbVb
but, keep the reaction stoichiometry in mind.
Diagram showing setup for titration procedures.
Chemical Titration
This process can be done for any reaction in which a stoichiometric equivalence is reached and can be identified by an indicator
At the equivalence point an indicator will change color permanently.