quantum mechanics Flashcards

1
Q

what is the rydberg equation?

A

v(frequency) = Rh [1/n (initial) ^2 - 1/n (final)^2 ]

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the rydeberg equation used for?

A

to calculate the frequency of light when an electron moves form one orbital to another.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what does n (initial) equal in the Balmer series

A

2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what does n (initial) equal in the Paschen series

A

3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what does n (initial) equal in the Lyman series

A

1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what type of light is used for the Lyman series

A

ultra violet

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what type of light is used for the Balmer series

A

visible

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what type of light is used for the paschen series

A

infrared

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what happens if you are able to fully remove an electron from an atom (move it up an infinite number of shells.)

A

the n (final) becomes infinity, any number over infinity is 0. (this is the same thing as ionisation energy.)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

when the Rydberg equation to calculate the ionisation energy, the infinity should go _____ and the second value should be ______

A

first, stated in the question

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is the de Broglie equation?

A

wavelength = h/mv (velocity)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

when would you use the de Broglie equation ?

A

when calculating the wavelength of a moving object

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what does the Heisenberg uncertainty principle state ?

A

it is impossible to predict both the precise position and momentum of an object. - the more precise that we know the of the location, the more uncertain the momentum will become and vice versa.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is the equation for the Heisenberg uncertainty principle?

A

delta p . delta q >= h/4pi

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

how do you calculate the change in momentum ?

A

since p=mv
delta = m . deltav

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what element is the schrodinger equation used for and why?

A

hydrogen, as it only has 1 electron.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

what does H^ stand for and what does it hold?

A

the Hamiltonian operator, and it holds all the info on the conditions of the atom.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

what is the Schrödinger equation

A

H^ Y(wave function symbol) = E Y( wave function symbol)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

what is the equation (linked to the Schrödinger equation), which helps us find the energy for the different hydrogen orbitals?

A

En = - hR/n^2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

what is an orbital?

A

an orbital is the region of space defined by the wave function

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

what does the radial wavefuntion describe ? [R(r)]

A

the distance of an electron from the nucleus of an atom

22
Q

what does R(r)^2 stand for

A

the radial probability density

23
Q

what does the radial probability density show us ? [R(r)^2]

A

The probability of finding the electron at a point located distance r from the proton.

(This is important to use as a square number can never be negative. )

24
Q

what is the equation for the radial distribution function?

A

4pi(r)^2R(r)^2

25
draw the graph of R(r) for a 1s orbital
exponential decay from 1
26
draw the graph of R(r) for a 2s orbital
exponential decay from 1 and a dip below the x axis.
27
draw the graph of R(r) for a 2p orbital
starting from 0 straight up to 1, then an exponential decay back to 0.
28
draw the graph of R(r) for a 3s orbital
exponential decay from, a dip below the x axis and a hump above the x axis.
29
draw the graph of R(r) for a 3p orbital
starting from 0 straight up to 1, then an exponential decay back to 0, with an dip below the x axis
30
draw the graph of R(r) for a 3d orbital
same as 2p, but a less steep line up to 1 from the origin.
31
what do the graphs look like for R(r)^2
in tetxbook - s starts from 1 never drops below 0
32
draw the graphs for the radial distribution function against r
in textbook - all start from origin - extra waves are smaller before the big wave - never drops below 0
33
when does a node exist?
where there is a 0% chance of finding an electron. where R(r)=0
34
what helps you determine the number of radial nodes?
n - l - 1 = number of radial nodes
35
where there is no nodes there is ....
0 probability of finding an electron
36
what helps you determine the number of angular nodes?
It is equal to the value of l
37
draw the d xy orbital
in between the x and y axis
38
draw the d yz orbital
in between the z and y axis
39
draw the d xz orbital
inbetween the x and z axis
40
draw the x^2 - y^2 orbital
lies on the x and y axis
41
draw the z^2 orbital
p orbital along the z axis and a ring around the centre
42
what is the Pauli exclusion principle
No 2 electrons in the same atom can have the same 4 quantum numbers.
43
what is aufbaus principle
orbitals much be filled in order of increasing energy
44
what is hunds rule
When filling a set of degenerate orbitals, electrons are added with parallel spins to different orbitals.
45
for what elements is hunds rule broken
chromium and copper
46
what is the order of better shielding
s>p>d>f
47
how do you find the total nuclear charge on a nucleus
the number of protons
48
draw a 3p orbital
49
draw a Pz orbital
only side on one
50
strong s-p mixing occurs when s and p have ____
similar energies - elements bonding up to carbon is normally considered to have strong s-p mixing
51
why are 2s orbitals more penetrating than 2p orbitals?
(higher probability of finding an electron.) The presence of the radial node of the 2s orbital mean sit has an area of high electron density close to the nucleus, which the 2p doesn't. The 2s electron is said to penetrate the 1s electron and thus the 2s electron feels higher effective nuclear charge than the 2p electron. The 2s orbital is therefore more stabilised than the 2p orbital.
52
what does u mean
when the orbital is inverted it experiences a phase change.