topic 4 Flashcards

1
Q

what changes across a node

A

the sign of the wave function

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2
Q

which d orbitals lie between the cartesian axis

A

dxy
dzy
dzx

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3
Q

which d orbitals lie on the cartesian axis

A

dz^2
d x2 - y2

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4
Q

what does orbital energy depend on

A

depends on the e- inside of them

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5
Q

what is the orbital energy when there are no e- inside them

A

0 orbital energy when the orbital is empty

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6
Q

where are d orbitals degenerate

A

they’re degenerate in:
a vacuum
a spherical field of negative charge

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7
Q

what is the difference between d orbitals in a vacuum and in a spherical field of negative charge

A

in the spherical field, the orbitals have higher energy but are still degenerate

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8
Q

what is the crystal field theory

A

an ionic model that considers metals and ligands as point charges

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9
Q

what are the point charges of the metal and ligand

A

M = +

L = -

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10
Q

what holds the metal ligand complex

A

the electrostatic forces of attraction between the M+ and L-

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11
Q

what interaction does CFT focus on

A

how the interaction of the ligand and metal affects the d orbital energy

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12
Q

what can CFT explain

A

spec
magnetism
reactivity trends in d block compounds

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13
Q

when an octahedral complex is affected by a crystal field, what happens

A

5 splits into
2 eg (higher energy - directed towards ligands)
3 t2g (lower energy - lie between ligands and the cartesian axis )

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14
Q

what is the crystal field splitting energy for octahedral complex’s

A

🔺o

separation between eg and t2g

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15
Q

what factors affect magnitude of 🔺o

A
  • nature of metal
  • metal charge
  • metal group position
  • ligand
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16
Q

how does the metal charge effect 🔺o

A

higher + charge = higher oxidation state
= smaller metal ion
= shorter ML bond distance
= stronger interaction energy
= larger 🔺o

17
Q

how does the metals group position affect 🔺o

A

🔺o increases by 20%-50% for each successive TM row

larger size = larger overlap with ligand

18
Q

what ligands cause a larger 🔺o

A

halides = slow separation

CN- , CO= strong binding = toxic = larger 🔺o

19
Q

what TM make a tetrahedral shape

A

mostly first row TM

20
Q

how do tetrahedral complex’s split in a crystal field

A

3 = t2 = higher energy (closer alignment to ligands)

2 = e = lower energy ( low alignment to ligands)

21
Q

what is different to the splitting in tetrahedral and octahedral complexes

A

in tetrahedral complexes, no orbital align exactly to the ligand

22
Q

what is the crystal field splitting energy gap in tetrahedral complex’s

A

🔺t

23
Q

what is eg

A

high energy
octahedral
doubly degenerate 2

24
Q

what is e

A

lower energy
tetrahedral
doubly degenerate 2

25
Q

what is t2

A

high energy
tetrahedral
triply degenerate

26
Q

what is t2g

A

low energy
octahedral
triply degenerate