Week 2 Module 1 Flashcards

1
Q

What word is interchangable with orbital?

A

Wave function.

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2
Q

What is the 1s orbital and si1s^2 orbitals relationship with 0?

A

They almost reach 0 but only end up approaching for infinity.

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3
Q

What do we have to think about when we think about probability density?

A

Shells - the probability of finding an electron in a particular shell.

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4
Q

What is the thickness of an electron shell?

A

Δr, therefore thickness increases with r.

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5
Q

Explain radial probability density of si1s^2.

A

r=o being 0 chjecks out as r=0 is like a tiny dot and vry close to the nucleus. Prob is also around 0 when r is very large. Inbetween, there is a curve with a maximum probability. “There is a maximum probability point that is somewhat away from the origin

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6
Q

How many nodes are there in the 2s orbital? What does this mean?

A

There is 1 nod, - there is a more complex 1d and 2d wave.

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7
Q

What does the graph of the 2s orbital look like?

A

We start off at a maximum point which decreases, touches 0 at the node, and goes in the negative region of the amplitude where it curves back and approaches 0 as r increases.

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8
Q

Explain the radial probability density of 2s orbital.

A

At the node, the wave function amplitude = 0, si2s = 0 at node.
Also 0 at origin and basically 0 at a large r.

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9
Q

Where is the most probable place to find electrons in a 2s radial probability density?

A

Around 0.3. The probability is actually higher than for 1s orbital.

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10
Q

What is energy directly proportional to in shells?

A

The number of nodes. More nodes = higher energy = more complex.

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11
Q

Where can atoms be in a radial probability density?

A

Anywhere above 0 , just at different probabilities.
Concept exists because of the wave characteristic (?)

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12
Q

What is the 3D shape of the 3s orbital and what does it mean?

A

Spherical meaning no matter what firection you go the graph stays the same.

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13
Q

How many nodes does the 3s orbital have?

A

2 nodes, making it more complex than the 2s orbital. - refer to page 10 for the radial probability density.

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14
Q

What increases the size of an orbital?

A

n.

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15
Q

Are all orbitals spherically symmetrical?

A

No.

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16
Q

What does the subscript z in 2pz signify?

A

That it is orientated on the z axis/ in the z direction.

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17
Q

How many lobes does dyz orbital have?

A

4 lobes seperated by 2 nodal planes - amplitude of 0.

18
Q

What are 3D blobs called?

A

Nodes - regions of a 3D wave.

19
Q

What do you get if you square the wavefunction of a non-spherical orbital?

A

It still gives the probability.

20
Q

What happens to the shape of a non-spherical orbital if you square it?

A

It changes the lobe shape slightly but general features remain.

21
Q

How many P orbitals are there and how many D orbitals are there?

22
Q

What is the quantum number n?

A

The principle QN as it determines the size of the orbital and is involved in the other numbers l and m. Can be 1,2,3… etc. n is the number in front in 1s, 2p, 3d etc.

23
Q

What does n determine?

A

The energy. Therefore 2p and 2s have the same energy.”

24
Q

n example.

A

En ∝ -(1/n^2)

25
What does λ = n(/h??)/(mxu) show?
That electrons have both wavelength and momentum. (m x u)
26
What is the quantum number for orbital angular momentum?
l. It is related ti the principal number n. Called the azimuthal quantum number.
27
What values can l take on?
Any value between 0 and n-1.
28
What values can the Magnetic Quantum Number m take on?
Related to l in such a way that m can be = -l, ..., 0, ..., l.
29
What is m if l = 1?
m = -1, 0 , +1 (3 x 2p orbitals)
30
What are the 3p orbitals on an axis?
x, y, and z.
31
What do the values of l mean for the type of orbital?
l=0 is s, l=1 is p, l=2 is d and l=3 is f
32
What do the restrictions on the values of l and m do?
Make some orbitals impossible. eg. 1p, 2d, 3f are impossible as l must be less than n.
33
Explain the 3d orbitals also with QN.
n=3, l can be 2 (d orbitasls). Think of 3d/s as spherical but no nodes. When l = 2, -2<=m<=2. Therefore there are 5 different 3d orbitals. 3 are drawn using different xyz axis, one is dx^2-y^2 and the other is dz^2. 5 possible values correspond to 5 orbitals.
34
What is the attractive potential between proton and electron?
V(r) = -e^2/(4πε(o)r) or v(r)∝-1/r. The closer to the nucleus the electron is, the higher electron potential. (wave property prevents anything from happening.)
35
Ĥψ = Eψ
Ĥψ is kinetic potential.
36
t does solving the wave equation for a paticular potential energy function tell us?
1. The wavefunction. 2. Value for the energy E.
37
What is quantisation?
Quantization is the process of converting continuous, infinite values into a smaller set of discrete, finite values
38
Explain transition between levels?
Electrons can jump to different levels.
39
What does electron transition between levels require?
Energy that is equal to the difference in the energy levels. Goes up with the absoption of a photon and reemits it when it goes back down.
40
Explain allowed energy.
En = -(2 x π^2 x m x e^4)/(h^2 x n^2). Can be simplified with the Rydberg constant 2.18 x 10^-18 to be -2.18 x 10^-18 x n^2. This equals -Eᴿ 1/n^2