Ch 8: Acids and Bases
SUMMMARY
Acids and Bases
Theory |
Acid |
Base |
Arrhenius |
Produces H+ in solution |
Produces OH– in solution |
Bronsted – Lowry |
H+ donor |
H+ acceptor |
Lewis |
Electron pair acceptor |
Electron pair donor |
HA |
+ |
H2O |
→ |
H3O+ |
+ |
A– |
Acid |
Base |
Conjugate Acid |
Conjugate Base |
Acid Strength
Strong Acids
·Completely dissociate (ionize)
·Have weak conjugate bases
·HCl, HBr, HI, H2SO4, HNO3, HClO4, HClO3
Weak Acids
·Do not completely ionize
·Have a strong conjugate base
·CH3COOH
Water as an Acid and a Base
Amphoteric Substances
·Behave like acids and bases
·H2O, NH3, HSO4–
Ionization of Water
H2O + H2O → H3O+ + OH–
Hydronium Ion
Ionization of Water simplified
H2O → H+ + OH–
At 25°C, [H+] = [OH–] = 1.0 x 10-7 moles / L
[H+] x [OH–] = 1.0 x 10-14 = Kw
In a neutral solution, [H+] = [OH–] (pH = pOH)
In an acidic solution, [H+] > [OH–] (pH < 7.0)
In a basic solution, [H+] < [OH–] (pH > 7.0)
.
The pH Scale
pH = – log [H+]
pOH = – log [OH–]
pH + pOH = 14
In a neutral solution, pH = pOH
In a basic solution, pH > pOH Note: the higher the [H+], the lower the pH
In an acidic solution, pH < pOH e.g. [H+] = 1 x 10-6, pH = 6
[OH–] = 1 x 10-8, pOH = 8
.
Buffers
A buffer is a solution is a solution of a weak acid and its conjugate base.
e.g. 0.1 M acetic acid and 0.1 M sodium acetate
A buffer resists pH change.
Recall the weak acid acetic acid is largely unionized:
CH3COOH + H2O → CH3COO– + H3O+
95% 5%
Adding strong OH– or H+ produces almost no pH change because they react with the conjugate acid or base, respectively.
See:
http://www.wwnorton.com/college/chemistry/chemistry3/ch/17/chemtours.aspx
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Acid Base Ionization
Self-ionization of Water:
http://cdn.wwnorton.com/college/chemistry/chem3/chemtours/chapter_17/self_ionization/Interface.swf
Note: An excellent animation of the relative strength of acids is found at:
Acid Strength and Molecular Structure
http://media.wwnorton.com/college/chemistry/chemtours/chapter_17/acid_strength/interface.swf
Additional animations:
http://media.wwnorton.com/college/chemistry/chemtours/chapter_17/ph_scale/interface.swf
http://media.wwnorton.com/college/chemistry/chemtours/chapter_17/strong_titrations/interface.swf
http://media.wwnorton.com/college/chemistry/chemtours/chapter_17/buffers/interface.swf
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A good review of the inductive effect of electronegativity on relative acid strengths can be found at:
.
http://en.wikipedia.org/wiki/Acids