Schrodinger Wave Equation Flashcards

1
Q

What is the Schrodinger wave equation used for?

A

Determining the energy levels for electrons.

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2
Q

What is a wavefunction?

A

A mathematical function that varies with position.

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3
Q

What does each wavefunction describe?

A

A different orbital type with a characteristic energy.

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4
Q

What is the purpose of the wavefunction squared?

A

The wavefunction alone is not a measurable quantity, whereas the wavefunction squared is. It represents the electron density per unit volume.

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5
Q

What does dt measure?

A

How electron density varies as one moves through space in small volume amounts - this gives us orbital shape.

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6
Q

When was the SWE solved and what was the outcome?

A

In 1927 the equation was solved and it showed that the Bohr radius of 0.529 angstroms was the most likely distance from the nucleus of finding an electron in a hydrogen atom.

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7
Q

What is n?

A

Principle quantum number, determines the energy.

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8
Q

What is l?

A

Secondary quantum number, gives orbital type.

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9
Q

What is ml?

A

Magnetic quantum number, gives the orbital orientations for each l value.

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10
Q

What is R(r)?

A

The radial wavefunction and examines how the wavefunction changes as r varies. (r=distance from nucleus).

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11
Q

What is Y(theta, thing)?

A

The angular wavefunction and determines the overall orbital shape.

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12
Q

What is a node?

A

When the wavefunction has a value of zero.

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13
Q

What are the two types of node?

A

A radial node and a nodal plane.

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14
Q

What does the radial wavefunction tell us?

A

How the wavefunction behaves as a function of distance from the nucleus only.

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15
Q

What does R(r)^2 tell us?

A

The electron density at a specific point in space as a function of distance from the nucleus only.

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16
Q

Whys is R(r)^2 not that useful?

A

Does not take into account the amount of space (volume elements/places) available for the electron and can be misleading.

17
Q

What is the radial distribution function?

A

The probability of finding an electron in a spherical shell of thickness dr at a distance r from around the nucleus.

18
Q

What does the maximum in the rdf tells us?

A

The most probable distance from the nucleus of finding an electron.

19
Q

What is a key difference between s orbitals and all other orbitals in terms of R(r)?

A

S orbitals have a positive value of R(r) at the nucleus whereas all other orbitals have a value of R(r) of zero at the nucleus.

20
Q

Despite the 2s orbital having a greater rdf. max than the 2p orbital, why is a 2p electron more likely to be found further away from the nucleus than the 2s?

A

The 2s penetrates the 2p, so the 2s electron can sometimes get closer to the nucleus than the 2p electron. The energy of the 2p orbital is therefore greater than the 2s orbital, and the 2s fills before the 2p.

21
Q

How does the angular wavefunction vary for the pz orbital?

A

It is only dependent on theta and not phi.

22
Q

How does the angular wavefunction vary for the px and py orbitals?

A

The vary with both parts of the angular wavefunction but in different ways.

23
Q

What is a boundary surface?

A

Depictions of orbitals where there is 95% probability of finding an electron/where electron density is located.

24
Q

What are angular nodes?

A

When the angular wavefunction is equal to zero. They can be planes or cones and do not depend on r.

25
Q

Why must orbital approximations be used when looking at more than 1-electron systems?

A

The SWE cannot be solved if more than one electron is present.

26
Q

What is a radial node?

A

A distance from the nucleus (r) where the radial wavefunction is equal to zero.

27
Q

What is the orbital approximation?

A

Wf (1,2,3,4…N) = Wf1 x Wf2 x Wf3….n