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Problems
1. A. McQuarrie, page 120, #3-3 Show Af(x) = λf(x), for λ constant. Find the
eigenvalue λ.
B. McQuarrie, page 120, #3-4
C. McQuarrie, page 182, #4-11
2. McQuarrie, pages 121-122, #3-11. Continuity of ψ’
3. A. McQuarrie, page 123, #3-17
4. Particle in an infinite 1-D Well
A. McQuarrie, page 122, #3-12. Answer this problem qualitatively by drawing
a cartoon for n = 2 and n = 3 states.
B. Is there a simple mathematical/physical reason why the probabilities are
not 1/4 for all four regions: 0 ≤ x ≤ a/4, a/4 ≤ x ≤ a/2, a/2 ≤ x ≤ 3a/4, and
3a/4 ≤ x ≤ a?
[HINT: where are the nodes in ψn(x)?]

5. Particle on a Ring Solve for the energy levels of the particle confined to a
ring as a crude model for the electronic structure of benzene. The two
dimensional Schr¨odinger Equation, in polar coordinates, is
For this problem, U(r, φ) = ∞ for r = a, but when r = a, U(a, φ) = 0.
A. This implies that ψ(r, φ) = 0 for r = a. Why?
B. If ψ(r, φ) = 0 for r ≠ ɑ, then What is the simplified form of the
Schrȍdinger Equation that applies when the particle is confined to the ring?
C. Apply the “periodic” boundary condition that ψ(a, φ) = ψ(a, φ + 2π) to
obtain the En energy levels.
6. 1-Dimensional Infinite Wells with Steps
Consider the potential
(This is the energy of n = 1 of an infinite well of width a/2.)

A. Sketch V (x) vs. x.
B. What are the boundary conditions for ψ(x) at x = 0 and x = a?
C. What requirements must be satisfied at x = a/2?
D. Solve for the n = 2 (one node) and n = 3 (two nodes) ψn(x) eigenfunctions
of Ĥ and En energy levels.
Hints:
E. Compare your values of E2 and E3 to what you obtain from the de Broglie
quantization condition

F. For the n = 2 and n = 3 energy levels, what are the probabilities, P2 and P3,
of finding the particle in the 0 ≤ x ≤ a/2 region?
G. (optional) Will the n = 2 and n = 3 energy levels of the V1(x) and V2(x)
potentials (defined below) be identical, as suggested by part E? Why?
versus
H. Solve for n = 1 ψ1(x) and E1 for V1.
HINTS: For a/2 < x ≤ a,
I. (optional) Is E1 for V1 larger or smaller than E1 for V2? Why? A cartoon would
be helpful.

1 A. McQuarrie, page 120, #3-3 Show Af(x)= λf(x), for λ constant. Find the eigenvalue λ.
(a)
(b)
Solutions

C. McQuarrie, page 182, #4-11
(a) The Commutator [Â, B] = − BA operates on f(x).

(There’s no particularly good notation for this type of operation.)

2. McQuarrie, pages 121-122, #3-11. Continuity of ψ0 Solution:
Beginning with the Schrȍdinger equation
we integrate both sides from a − ε to a + ε (taking the limit ε → 0), where a is some
arbitrary fixed value of x,

If the left side of Eq 2.3 is 0, then by definition dψ/dx is continuous at x = a. The right
side of Eq 2.3 is obtained by noting than in the limit that ε → 0, the integral about x =
a is just equal to the integrand evaluated at x = a (if the integrand is continuous) times
the width of the integration limits, which is simply 2ε. Since this first case assumes V
(x) is continuous, and since ψ(x) is always continuous, we can perform this “rigorous
limiting approximation.” (Apologies if that sounds like an oxymoron). Since (V (a) −
E)ψ(a) is just some constant number, the limit on the right hand side of Eq 2.3 is equal
to 0. Therefore, the condition for continuity of dψ/dx at x = a is satisfied. Since a was
an arbitrary value for x, dψ/dx must be continuous everywhere.
If V (x) is not continuous at x = a, then we need to split up the integral into two parts

In the last step, we replaced V (a−) with the limiting value of V (x) on the left side of
the discon-tinuity V` (and similarly for V (a+)). Since ψ(x) is continuous, both limits are
equal to its value at x = a. Examining this limit, we see that even though V` = Vr, both
are still finite numbers. Therefore, the limit (which is ∝ ε), still goes to 0. Thus the left
side of Eq 2.3 is still zero, and dψ/dx is continuous even at finite discontinuities in V
(x).
In the case that V (x) has an infinite discontinuity at x = a (e.g. a particle in a box
potential), then either V` or Vr is infinite. The limit as ε → 0 of Eq 2.6 won’t be zero,
but some finite number (“ 0 ×∞ ∼ finite”). Therefore, by Eq 2.3, dψ/dx will have
different limiting values depending on which direction you come from. Thus, we’ve
shown that the derivative of the wavefunction is discontinuous at infinite boundaries.
3. A. McQuarrie, page 123, #3-17
For a particle in a box of extent [0,a], we have the normalized eigenfunctions
The expectation values, hxi and hx2i, for the state ψn are

This yields

Therefore, the uncertainty σx is always less than a, the width of the box. Since we know
the particle cannot be outside the box (where V = ∞), it makes physical sense that the
uncertainty in position can never be larger than the width of the box.
In this problem, we apply the de Broglie hypothesis to standing waves in the particle
in a box potential. We posit that the waves in the allowed region must satisfy
so that nodes occur at the end points and there are an integral number of
half-wavelengths within the box. Using the de Broglie hypothesis to solve for the
corresponding momenta, we obtain
The resulting energies match the energy eigenvalues obtained from solving the
Schr¨odinger equation.

4. Particle in an infinite 1-D Well
A. McQuarrie, page 122, #3-12. Answer this problem qualitatively by drawing
a cartoon for n = 2 and n = 3 states.
The solutions for a particle in an infinite box of length a are
The number of internal nodes is n − 1. The nodes are equally spaced. There is an
equal probability of the particles being in each of the lobes of ψ(x).
The probabilities in the four equal regions are not equal, which is illustrated by
the sketch for n = 2 and n = 3.
The cartoons that show the difference in probability for regions of width a/4
for n = 2 and n = 3.

B. Is there a simple mathematical/physical reason why the probabilities are not 1/4 for
all four regions: 0 ≤ x ≤ a/4, a/4 ≤ x ≤ a/2, a/2 ≤ x ≤ 3a/4, and 3a/4 ≤ x ≤ a? [HINT: where
are the nodes in ψn(x)?]
Compute the probabilities in the four equal length regions for any value of quantum
number n. Probability in region c ≤ x ≤ d
From integral table
Compute the probabilities
First Region: 0 ≤ x ≤ a/4 c = 0, d = a/4
Second Region: a/4 ≤ x ≤ a/2 c = a/4,d = a/2

Third Region a/2 ≤ x ≤ 3a/4 c = a/2,d =3a/4
Fourth Region 3a/4 ≤ x ≤ a c =3a/4,d = a
Overall we get probability
The sum over all 4 regions is 1, but the probability is not 1/4 in each of the 4
regions as you saw from the cartoons in part A.

5. Particle on a Ring
Solve for the energy levels of the particle confined to a ring as a crude model for the
electronic structure of benzene. The two dimensional Schrȍdinger Equation, in polar
coordinates, is
For this problem, U(r, φ)= ∞ for r = a, but when r = a, U(a, φ) = 0.
A. This implies that ψ(r, φ)=0 for r Why?
We begin with the two-dimensional Schr¨odinger equation in polar coordinates (r, φ),
where
Just like the particle in the box, wherever the potential is infinite, the wave function
must be zero. Otherwise, the Schrȍdinger equation would diverge. Therefore ψ(r,
φ)=0 for r = a.

B. If ψ(r, φ)=0 for r = 0. What is the simplified form of the Schr¨= a, then ∂ψ odinger
Equation ∂r that applies when the particle is confined to the ring?
Since ∂ψ = 0, the first term in the brackets of Eq. 5.1 is 0. Additionally, we can replace
r with a ∂r everywhere else. Since U(a, φ) = 0, this term also vanishes. We are left
with
C. Apply the “periodic” boundary condition that ψ(a, φ)= ψ(a, φ +2π) to obtain the En
energy levels.
Eq. 5.3 can be rewritten as
which has solutions
Applying the periodic boundary condition ψ(φ)= ψ(φ +2π) gives us

Now solving for E in terms of m,
The quantized energy levels are ∝ m2 and for |m|≥ 1 occur in degenerate pairs of
{±m}.
D. The C–C bond length in benzene is 1.397 ˚A. Thus a circle which goes through all 6
carbon atoms has a radius r =1.397 ˚A. Use this to estimate the n =2 ← n = 1 electronic
transition for “benzene” treated as an electron on a ring. The longest wavelength
allowed electronic transition for real benzene is at 2626 ˚A. Explain why the
agreement is not perfect.
Solution:
Approximating the electronic structure of benzene as a particle on a ring, with a
= calculate the m = 2 ← m = 1 transition to lie at

This is fairly close to the experimental value of 2626 ˚ A)2 1.397 ˚ A, we (5.12)
(5.13) (5.14) (5.15) A, indicating that the particle on a ring is a qualitatively correct
picture of benzene’s electronic structure. There are various reasons for the
discrepancy, however. First, the potential is not uniform with φ, but has periodic
wells near each carbon atom. Additionally, electron-electron repulsion will
significantly change the multi-electron orbital energies (which we do not account
for in this simple one-electron state model).
[Note: if you are confused why we use the 2 ← 1 transition instead of the 1 ←
0, consider how many “ring electrons” there are in benzene. What electronic
states (i.e. orbitals) are filled? What transition corresponds to the longest
wavelength?]
6 1-Dimensional Infinite Wells with Steps
Consider the potential
(This is the energy of n = 1 of an infinite well of width a/2.)
A. Sketch V (x) vs. x.

B. What are the boundary conditions for ψ(x) at x = 0 and x = a?
Solution: ψ(0) = ψ(a)=0
C. What requirements must be satisfied at x = a/2?
D. Solve for the n = 2 (one node) and n = 3 (two nodes) ψn(x) eigenfunctions of H
band En energy levels.
Hints: eduassignmenthelp.com

Solution: The matching requirements at x = a/2 are

To simplify the algebra, let k0 = kIa/2, k0 I II = kIIa/2
Combine Eqs. (6.1) and (6.3) and solve using Wolfram Alpha.
We get pairs of k0 and k0 I II.

So we get the first three energy levels:
We take these values of E and input them to the original forms of ψI, ψII, and dψII and
solve dx dx for the values of A and B, and finally normalize the ψi(x).
Solution: The de Broglie quantization condition is based on the requirement that ψ(0)=0 and
ψ(a) = 0. We have two segments of the wavefunction which have
λ = h/p.
For n = 2 we expect one internal node, so there will be one full wavelength. For n = 3 we
expect two internal nodes so there will be 3/2 wavelength. We calculate the accumulated
phase in the 0 ≤ x ≤ a/2 and a/2 ≤ x ≤ a regions.

F. For the n = 2 and n = 3 energy levels, what are the probabilities, P2 and P3, of finding
the particle in the 0 ≤ x ≤ a/2 region?
The relative probabilities of finding the particle in the 0 ≤ x ≤ a/2 and a/2 < x <
a regions are proportional to the reciprocal of the momentum. The particle
moves faster in Region I than in Region II.
The semi-classical (WKB) quantization condition may be expressed as an “action
integral”
where pn(x) is the classical momentum
n = 1, 2,... is the integer quantum number, the number of internal nodes in ψn(x)
is n − 1, the inner and outer turning points are x<(En) and x>(En), and En is the
nth eigenenergy. The quantity p(x)dx is “action”. The −1/2h term on the right
hand side corresponds to extra stabilization due to accumulation of action outside
of the classically bounded region which is required to permit lim|x|→∞ ψ(x) = 0.

However, in the case of infinite vertical walls, the −1/2h term is not present. The
de Broglie relation, λ = h/p, becomes a basis for intuition. If V (x) is piece-wise
constant, then the fractional number of wavelengths in each constant V (x) region
is
We are interested in the integer number of half-wavelengths between turning
points. If V (x) is piece-wise constant, then the number of 1/2-wavelengths in
each constant–V (x) region is
The ψn(x) for the n = 1, 2, 3 levels have 1, 2, 3 half-wavelengths. The two
regions of the V (x) are each of length a/2 and
The relative probabilities are proportional to
P rel I ∝ 0.7820 P rel II
Normalize for n = 2:
PI = P rel I E = p 2/2m [(0.7820)2 +
(1.256)2]−1/2 = 0.384
PII = 0.616

Notice that the probabilities in the two regions become more nearly equal as
the energy increases. This illustrates how the effect of the step is felt less as E
increases, eventually becoming negligible at very high E.
G. (optional) Will the n = 2 and n = 3 energy levels of the V1(x) and V2(x)
potentials (defined below) be identical, as suggested by part E? Why?
versus
This is the most important part of this problem. It asks you to create a
cartoon that is built on all of the crucial insights of this problem:
1. The lowest energy level of any one dimensional problem has zero internal
nodes.
2. Tunneling into a classically forbidden region always results in stabilization
relative to a zerotunneling situation.
3. The wavefunction in a classically forbidden region always has the form:

4. When the potential energy is stepwise-constant, κ is independent of x
and it is often convenient to assume that A and B are positive or negative
real numbers.
5. A crucial point is that at every internal joining point, xjoin, there are two
requirements, continuity of the wavefunction and continuity of its derivative,
dψ/dx. At a boundary, at xstep, to a region where V (x) discontinuously
becomes infinite, there is only one requirement: ψ(xstep) = 0. There is no
requirement on dψ/dx. (You know this from the particle in an infinite well.)
For this specific problem, V (x) = ∞ for x < 0 and x > a, V (x) = 0 for x ≥ 0
and x ≤ a, with a barrier of width a/2 and height V0 = h2/8m(a/2)2 , V0 is
chosen to be the exact energy of the n = 1 level of a particle in an infinite
well of width a/2 and the exact energy of the n = 2 level of an infinite well
of width a. So the crucial issue is how does the location of the barrier
within the box affect the energy of the n = 1 level. The problem is
constructed so that you address the crucial question: which placement of
the barrier, centered vs. right-side, results in the lowest energy?

This problem illustrates a shortcoming of a semiclassical “accumulated phase”
method for estimating eigen-energies, which involves complete neglect of joining-
point matching requirements. You might have guessed that the key insight is the
existence of two (centered barrier) vs. one (right-side barrier) internal matching
points.
6. Cartoons provide key insights
First insight: if, upon entry into the E < V0 barrier region, ψ(x) and dψ/dx have
the same sign, the absolute value of the wavefunction will increase exponentially.
This means that, for the barrier in the center, it will be impossible to satisfy the
continuity of derivative requirement at the midpoint of the barrier region, and for
the barrier on the right it will be impossible to satisfy the requirement that ψ(a)
= 0. For the barrier in the center, the energy of the n = 1 level must be larger
than V0. If E1 < V0, both ψ and dψ/dx will have the same signs at both x = a/4
and at 3a/4. Continuity of dψ/dx at x = a/2 cannot be satisfied. So the n = 1
level of the barrier in the center will be shifted to above the top of the barrier.
For the n = 1 level of the barrier on the right, in order to satisfy the ψ1(a) = 0
boundary condition, it is necessary for ψ1 and dψ1/dx to have opposite signs at x
= a/2. The lowest energy at which this could occur is for E1 slightly larger than
V0/4 (which is the energy of n = 2 of the barrier-free infinite well of width a)!
This demonstrates that the location of the barrier has an enormous effect of the
energy of the n = 1 level.

Second insight: For the barrier in the center, En=1 > V0, and so this will be a
simple 3-region problem and E must be determined (iteratively) so that ψ(a) = 0.
For the right side barrier, ψ(x) will be decreasing exponentially and E must be
chosen so that ψ(a) = 0.
Major insight about tunneling: For all symmetric wells with a barrier in the center,
the n = 1 level (no internal nodes) will be shifted upward from the no barrier
energy by a large amount, the n = 2 level (one node at the center) will be shifted
upward by a very small amount, and the n = 3 level (two nodes, neither at the
center) will be shifted upward by an amount much larger than that for the n = 2
level but much smaller than that for the n = 1 level. Level staggering is the
signature of tunneling!

I. (optional) Is E1 for V1 larger or smaller than E1 for V2? Why? A cartoon
would be helpful.
Solution: The form of ψII in the classically forbidden region for n = 1 is a
decreasing exponential. There can be no zero-crossing in the under-barrier
region. For the symmetric barrier, ψ(a/4) and ψ(3a/4) are smaller than ψ(a/2)
for the case of the right-side barrier. The rate of exponential decrease of ψ in
the forbidden region depends on V (x)− E. This means that the probability in
the forbidden region is larger for the right side edge barrier. This implies that
the energy is higher for n = 1 of V1(x).

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