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Lecture 1: Introduction and review

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Lecture 1: Introduction and review Quiz 1 Website: http://www.esf.edu/chemistry/nomura/fch530/ Review of acid/base chemistry Universal features of cells on Earth – PowerPoint PPT presentation

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Title: Lecture 1: Introduction and review


1
Lecture 1 Introduction and review
  • Quiz 1
  • Website http//www.esf.edu/chemistry/nomura/fch53
    0/
  • Review of acid/base chemistry
  • Universal features of cells on Earth
  • Cell types Prokaryotes and Eukaryotes

2
Review of pH, acids, and bases
  • pH is generally defined as the negative logarithm
    of the hydrogen ion activities (concentration)
    expressed over 14 orders of magnitude
  • pH -log10 H
  • The pH scale is a reciprocal relationship between
    H and OH-
  • Because the pH scale is based on negative
    logarithms, low pH values represent the highest
    H and thus the lowest OH-
  • At neutrality, pH 7, H OH-

3
Review of pH, acids, and bases
  • Strong electrolytes dissociate completely in
    water
  • Electrolytes are substances capable of generating
    ions in solution
  • Increase the electrical conductivity of the
    solution
  • The dissociation of a strong acid in water
  • The equilibrium constant is
  • H2O is constant in dilute aq. Solutions and is
    incorporated into the equilibrium constant.
    giving rise to a new term Ka-the acid
    dissociation constant KH2O, H3O is
    expressed as H

HCl H2O H3O Cl-
H3OCl-
K
H2OHCl
Because Ka is large for HCl, H in solution
HCl added to solution. Thus, a 1M HCl solution
has a pH of 0, a 1 mM HCl solution has a pH of 3,
and so on. Conversely, 0.1 M NaOH solution has a
pH of 13.
4
For a strong acid Ka will approach be large
because the nearly all of the protons will be
dissociated. The H at equilibrium is equal to
the initial concentration of the acid.
Calculate the pH of a 1M HCl solution
HCl H2O H3O Cl- 0.0004
at equilibrium 99.996 at equilibrium
Since we are at equilibrium, H3O is equal to the
initial concentration of acid.
H H3O HCl 1M
We know that pH is the -log of H, therefore
for 1M HCl at equilibrium
pH -log10 H
pH -log10 (1)
pH 0
5
pH
0 (100) 1.0 0.00000000000001 (10-14)
1 (10-1) 0.1 0.0000000000001 (10-13)
2 (10-2) 0.01 0.000000000001 (10-12)
3 (10-3) 0.001 0.00000000001 (10-11)
4 (10-4) 0.0001 0.0000000001 (10-10)
5 (10-5) 0.00001 0.000000001 (10-9)
6 (10-6) 0.000001 0.00000001 (10-8)
7 (10-7) 0.0000001 0.0000001 (10-7)
8 (10-8) 0.00000001 0.000001 (10-6)
9 (10-9) 0.000000001 0.00001 (10-5)
10 (10-10) 0.0000000001 0.0001 (10-4)
11 (10-11) 0.00000000001 0.001 (10-3)
12 (10-12) 0.000000000001 0.01 (10-2)
13 (10-13) 0.0000000000001 0.1 (10-1)
14 (10-14) 0.00000000000001 1.0 (100 )
6
Review of pH, acids, and bases
  • Weak electrolytes only slightly dissociate in
    water
  • Acetic acid, CH3COOH
  • The dissociation of a weak acid in water
  • The acid dissociation constant is
  • Ka is also called the ionization constant,
    because Ka is small, most of the acetic acid is
    not ionized.

CH3COOH H2O H3O CH3COO-
HCH3COO-
Ka
1.74 X 10-5 M
CH3COOH
7
Acid dissociation constant
  • The general ionization of an acid is as follows
  • So the acid dissociation constant is as follows

There are many orders of magnitude spanned by Ka
values, so pKa is used instead
pKa - log10 Ka
The larger the value of the pKa, the smaller the
extent of dissociation. pKa lt2 is a strong acid
8
Henderson-Hasselbalch Equation
  • Describes the dissociation of a weak acid in the
    presence of its conjugate base
  • The general ionization of a weak acid is as
    follows
  • So the acid dissociation constant is as follows
  • Rearranging this expression in terms of the
    parameter of interest H gives the following

HA H A-
HA-
Ka
HA
Ka
HA
H
A-
9
Henderson-Hasselbalch Equation
  • Take the log of both sides

log Ka log
logH
Change the signs and define pKa as -log Ka
pKa - log
pH
or
A-
pKa log
pH
HA
10
Titration curves and buffers
  • Titration curves can be calculated by the
    Henderson-Hasselbalch equation
  • As OH- is added to the reaction, it reacts
    completely with HA to form A-
  • x the equivalents of OH- added and V represents
    the volume of the solution. If we let co
    represent HA equivalents initially present, then
  • We can reincorporate this into the
    Henderson-Hasselbalch eqn.

A-
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