1 Problem 6.

2
A system is defined by the wavefunction:
 
2x L L
(x) = A cos for x
L 4 4
(a) Determine the normalization constant A.
(b) What is the probability that the particle will be found between x = 0
L
and x = ?
8

1.1 Solution
1.1.1 Part (a)
Z +
1= (x)(x)dx

L L
Z Z   Z
4 4 2x
1= 0dx + A2 cos2 dx + 0dx+
L
4
L L
4

Z L  
4 2x
1 = A2 cos2 dx
L
4
L
L
1 = A2
4
4
A2 =
L

1.2 Part (b)

Z L
L 8
P (0, )= (x) (x)dx
8 0
Z L 
L 4 2x
8
P (0, )= cos2 dx
8 0 L L
 
L 4 (2 + )L
P (0, ) =
8 L 16
L 2+
P (0, )= 0.41
8 4

1
2 Problem 6.5
A particle with zero energy has a wavefunction
x2
(x) = Axe L2
Find and sketch V(x).

2.1 Solution
Start with the Schrodinger Equation.

~2 d2 (x)
+ V (x)(x) = E(x)
2m dx2
Notice that the particle has zero energy.

~2 d2 (x)
= V (x)(x) (1)
2m dx2
Now to figure out the second derivative of the wavefunction. Make sure to
use the chain rule!
 
d(x) x2 2x x22
= A(1)e L2 + Ax e L
dx L2

2x2
 
d(x) x2
= A 1 2 e L2
dx L

d2 (x) 2x2
    
4x x22 2x x22
= A e L + A 1 e L
dx2 L2 L2 L2

d2 (x)
 3 
4x 6x x2

2
= A 4
2
e L2
dx L L
Now we can plug this and the original wavefunction back into Equation 1.

~2
 3 
4x 6x x2 x2
A 4
2
e L2 = V (x)Axe L2
2m L L
Now we can cancel a bunch of terms out to get

~2 4x2
 
6
V (x) =
2m L4 L2
This is an oscillators potential.

2
3 Problem 6.6
The wavefunction of a particle is given as

(x) = A cos(kx) + B sin(kx)

Show that it is a solution is the Schrodinger Equation with V(x)= 0 and
find the energy.

3.1 Solution
Start with the Schrodinger Equation.

~2 d2 (x)
+ V (x)(x) = E(x)
2m dx2
Theres no potential so

~2 d2 (x)
= E(x) (2)
2m dx2
Calculate the second derivative of the wavefunction

d(x)
= Ak sin(kx) + Bk cos(kx)
dx

d2 (x)
= k 2 (A cos(kx) + B sin(kx))
dx2
Plug this back into Equation 2

~2 k 2
[A cos(kx) + B sin(kx)] = E [A cos(kx) + B sin(kx)]
2m
So this is a solution to the Schrodinger Equation provided we have

~2 k 2 p2
E= =
2m 2m
Which is exactly what we would expect for a free particle.

4 Problem 6.11
L L
A particle is confined to a box from x
2 2
What are the wavefunctions and probability densities for the n = 1, 2, and
3 states? Sketch them.

3
4.1 Solution
The general solution for a particle in a box is still:

(x) = A sin(kx) + B cos(kx)

But now the boundary conditions are
L L
( ) = 0; ( ) = 0
2 2
The first of these tells us

0 = A sin(kL/2) + B cos(kL/2)
The second of these tells us

0 = A sin(kL/2) + B cos(kL/2)
The difference in sign is due to cos(x) being symmetric and sin(x) being
antisymmetric. Equating the two gives

A sin(kL/2) = A sin(kL/2)
But this only makes sense if A = 0, so the wavefunction is

(x) = B cos(kx)
Returning to the boundary conditions we have

0 = B cos(kL/2)
This means that
kL 1
= (n + )
2 2
So

k= (2n + 1)
L
This makes the wavefunction
 x 
n (x) = A cos (2n + 1)
L
Normalizing will still yield
p
A= 2/L
So
p  x 
n (x) = 2/L cos (2n + 1)
L

4
 This means the probability density will be
2  x 
Pn (x) = cos2 (2n + 1)
L L

5 Problem 6.24
A solution of Schrodingers equation for an oscillator is
2
(x) = Cxex
(a) Express in terms of m and . What is the energy of this state?
(b) Normalize it.

5.1 Solution
5.1.1 Part (a)
As always, start with the Schrodinger equation:

~2 d2 (x) 1 2
+ kx (x) = E(x)
2m dx2 2
Notice that this wavefunction is essentially the same as the one from problem
6.5 except we replaced L12 with . This means its second derivative will be:

d2 (x) 2
= C 42 x3 6x ex


dx 2

If we plug this into the Schrodinger Equation we get

~2 2 1 2 2
C 42 x3 6x ex + kx2 Cxex = ECxex


2m 2
This simplifies to

~2
1
42 x2 6 + kx2 = E (3)
2m 2
We can see that the x2 terms must cancel each other out, giving

~2 1
42 x2 = kx2
2m 2
Solving for alpha gives
r
km
=
4~2
Remember that
r
k
=
m

5
 Plugging this in gives
m
=
2~
The other consequence of Equation 3 is

~2
(6) = E
2m
This simplifies to

3~2
E=
m
Plugging in alpha gives
3
E= ~
2
Notice that this is the energy of a quantum harmonic oscillator in the n=1
state!

5.1.2 Part (b)

We have the standard rule for normalization
Z +
1= (x)(x)dx

Z +
2
1= C 2 x2 e2x dx

 r 
1 3/2
2
1=C
4 2
r r 
2 3/2 2 m 3/2 2  m 3/2
C2 = 4 =4 =
2~ ~

6 Problem 6.29
An electron is bound to x > 0 with the wavefunction

(x) = Cex 1 ex

(a) Normalize the wavefunction.

(b) What is the most probable value of x?
(c) What is the expectation value of x?

6
6.1 Solution
6.1.1 Part (a)
Again start with
Z +
1= (x)(x)dx

Z +
2
1= C 2 e2x 1 ex
0
 
1
1 = C2
12

C 2 = 12

6.2 Part (b)

We find the most probable value by finding where the derivative of the proba-
bility is 0:
d 
2 
0= 12 e2x 1 ex
dx
We can throw away the normalization constant, but must make sure to use
the chain rule

0 = (2)e2x (1 ex )2 + e2x (2)(1 ex )1 (ex )

Canceling terms and factoring gives

0 = (2ex 1)(1 ex )
The term in the right parentheses is only 0 when x = 0, but that is outside
the allowed range. This means

0 = 2ex 1
Which has the solution

x = ln 2 0.69

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6.3 Part (c)
To find the expectation value, we use
Z +
hAi = (x)A(x)dx

In our case this is:

Z +
2
hxi = 12 xe2x 1 ex dx
0
This works out to be
13
hxi = 1.1
12
This means that the most probable value is NOT the expectation value. This
is because the expectation value is just the average value. The most probable
value is just the highest point on the plot of P (x) vs x. If you have an asymmetric
curve, these two are not necessarily the same.

7 Problem 6.35
Which of the following are eigenfunctions of the momentum operator
d
p = i~
dx
(a) (x) = A sin(kx)
(b) (x) = A sin(kx) A cos(kx)
(c) (x) = A cos(kx) + iA sin(kx)
(d) (x) = Aeik(xa)

7.1 Solution
The generic eigenvalue problem for an operator A is

A = c
d
Where c is a constant and an eigenvalue of A. In our case A = p = i~
dx

7.2 Part (a)

d
i~ (A sin(kx)) = i~Ak cos kx 6= c(A sin(kx))
dx
So it is NOT an eigenfunction.

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7.3 Part (b)
d
i~ (A sin(kx)A cos(kx)) = i~k(A sin(kx)+A cos(kx)) 6= c(A sin(kx)A cos(kx))
dx
So it is NOT an eigenfunction.

7.4 Part (c)

d
i~ (A cos(kx)+iA sin(kx)) = i~(Ak sin(kx)+ikA cos(kx)) = ~k(A cos(kx)+iA sin(kx))
dx
So this IS an eigenvector with eigenvalue

c = ~k = p

7.5 Part (d)

d  ik(xa)   
i~ Ae = i~(ik)Aeik(xa) = ~k Aeik(xa)
dx
So this IS an eigenvector with eigenvalue

c = ~k = p

8 Additional Problem
8.1 Solution
The wavefunction is:
 1/2
2  m 3/2 2
(x) = xex
~
With
m
=
2~

8.1.1 Part (a)

Z +
hxi = (x)x(x)dx

2  m 3/2 3 2x2
Z
hxi = x e dx
~

hxi = 0
2
Since x3 is odd (antisymmetric) and e2x is even (symmetric), their prod-
uct is odd. Integrating an odd function over an eve interval will give zero

9
8.1.2 Part (b)
Z +
2
hx i = (x)x2 (x)dx

2  m 3/2 4 2x2
Z
2
hx i = x e dx
~
 r 
2 2  m 3/2 3 5/2
hx i =
~ 16 2
3 ~
hx2 i =
2 m

8.1.3 Part (c)

p p
x = hx2 i hxi2 = hx2 i
r
3 ~
x =
2 m

8.1.4 Part(d)
Z +
hpi = (x)p(x)dx

2  m 3/2 x2
Z  
d 2
hpi = xe i~ xex dx
~ dx
3/2
Z
2 m
  2 2
xex (i~) 1 2x2 ex dx


hpi =
~
These will both lead to odd functions being integrated over an even interval,
so we know it will go to zero.

hpi = 0

8.1.5 Part (e)

Z +
hp2 i = (x)p2 (x)dx

2
2  m 3/2 x2
Z 
d 2
2
hp i = xe i~ xex dx
~ dx
We already calculated the second derivative of this wavefunction, so we can
just plug it in

2~2  m 3/2 x2
Z
2
hp2 i = 42 x3 6x ex dx


xe
~

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 Z Z
2~2  m 3/2
 
2 2 4 2x2 2 2x2
hp i = 4 x e dx + (6) x e dx
~

2~2  m 3/2
  r   r 
2 2 3 5/2 1 3/2
hp i = 4 6
~ 16 2 4 2

2~2  m 3/2 1/2

r    
3 6
hp2 i =
~ 2 4 4
3
hp2 i = m~
2

8.1.6 Part (f )
p p
p = hp2 i hpi2 = hp2 i
r
3
p = m~
2

8.1.7 Part (g)

r r
3 ~ 3
xp = m~
2 m 2
3
xp = ~
2
~
This obeys the Heisenberg uncertainty principle, which says that xp .
2
If you repeat this for an n = 0 quantum harmonic ocillator, you will actually
~
get the minimum value of xp =
2

11