Let’s Talk About Beer
Beer’s Law and
Concentrations
Solution Concentration Reminders
Concentration
expresses how the
amount of solute
and the amount of
solution compare
Our unit of choice:
Molarity = mols/L
What do you notice
about the
solutions?
Why Does Color “Fade” as
Concentration is Lessened?
Conc is moles
(number of
ions/atoms/molecul
e) per space
More molecules
means more light is
“caught”
Examples
Beer’s Law
Beer’s Law quantifies
the relationship
between color and
concentration
Beer’s Law states that
the absorbance (why?)
of light by a solution is
directly proportional to
Emissivity
Cell width
concentration
So, What Does This Means
It means that a graph
of absorbance of light
by a “kind” of solution
TO the concentration
is linear.
It means that
predictions are
accurate and reliable
We can find
concentrations by
comparison
How Do We Do This?
We make several solutions with known
concentrations
We determine which wavelength or color of
light the solution responds to best
We measure that transmittance and/or
absorbance for the known solutions and the
unknown solution
We graph the knowns and interpolate for the
unknown
A Successive Dilution Example
Design a process of successive
dilution to make 250.0 mls of the
following solutions from a 0.85 M stock
solution: 0.50 M, 0.30 M, 0.10 M.
Why Not Transmittance?
Imagine an area enclosed by a curtain
containing a mystery number of people
Each person can catch and hold 2 tennis
balls
We throw 1000 balls into the area
We measure what comes out (Trans)
But we find the number of people by what
doesn’t come out (Abs)
# People is related to number of balls
caught (Abs)
Spectroscopy: The kind you
can see
Spectroscopy
involves the study
of light that is
absorbed or
emitted by a
substance
Visible spec.
involves light we
can see
The plan:
We’ll shine light that is absorbed well
into solutions of known concentration
We’ll make a plot of known
concentrations versus absorbance
We’ll test our unknown solution
We’ll interpolate to find the
concentration that matches its
absorbance
Great! How do we do that?
Calibrate the
machine
Find the best
wavelength (lmax)
Test all solutions at
that wavelength
Graph or use
“factor”
Calibration of Spec 20
Allow the machine to warm up
Set wavelength to desired value (400 nm)
With sample chamber empty set %T to zero
using left knob
With water (or some other solvent) in
sample chamber set %T to 100% using right
knob
Repeat for each wavelength
Finding lmax
Calibrate machine at 400 nm
Place one solution (usually a “middle”
concentration) into sample chamber
Record data
Reset machine to 425 (or 450) nm
Calibrate and test same solution
Repeat until you reach 750 nm
Testing the solutions &
unknown
Once you’ve found
the best
wavelength (light is
absorbed best) test
all solutions and
unknown at this
wavelength
Use data to find
concentration of
unknown
Finding the unknown
Suppose this graph is
generated
The unknown
absorbance is 0.500
Find 0.500 absorbance
Across and down
The concentration is
0.775 (or so)