atomic structure - orbitals Flashcards

(21 cards)

1
Q

atomic orbitals definition

A

probability regions of space that have particular shapes, where electrons are found

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2
Q

give the first 4 types of atomic orbital

A

s (sharp) = spherical
p (principle) = 2 lobes, 1 node
d (diffuse) = 4 lobes, 2 nodes
f (fundamental) = 6 lobes, 3 nodes

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3
Q

what are the 4 quantum numbers

A

n = principle QN - defines atomic shell/row of periodic table, can = any integer
l = angular QN, describes shape of orbital, can = any integer 1 -> n-1
ml = magnetic QN, described orientation of orbital relative to x, y, z, can = any whole no. from -l -> +l
ms = spin QN, can = +1/2 or -1/2

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4
Q

where do quantum numbers come from?

A

derived from schrodingers equations

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5
Q

what is the purpose of quantum numbers?

A

they describe/characterise an atomic orbital

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6
Q

what type of compounds are diamagnetic?

A

compounds with paired electrons

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7
Q

what type of compounds are paramagnetic?

A

compounds with unpaired electrons

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8
Q

how does orbital energy increase between shells?

A

n=1 < n=2 < n=3 < n=4 … going out further from nucleus energy increases

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9
Q

within shells how does orbital energy increase?

A

s < p < d < f … as angular QN l increases

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10
Q

what is the difference between a radial node and an angular node?

A

radial nodes - where radial function in wave function = 0 - sphere
angular nodes - where angular function in wave function = 0 - flat plane

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11
Q

what is the purpose of the Bohr-Bury rules

A

they describe the energy of orbitals

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12
Q

what are the 2 Bohr-Bury rules?

A

1- energy of an orbital is determined by n+l (principle QN + angular QN)
2- when 2 orbitals have the same n+l values, orbital of lower n value is lower in energy

  • this dictates the order of filling
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13
Q

what are the 3 types of wavefunction graphs?

A

R(r) - standard wavefunction = atomic orbital, a single electron wavefunction
(R(r))^2 - wavefunction squared = probability density of finding an electron at a particular location
rdf- wavefunction x 4πr^2 - probability of finding electron within small radial space around nucleus

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14
Q

what does the maxima of an rdf graph represent?

A

the most probable distance from nucleus where the electron will be found

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15
Q

why is R(r)^2 always positive?

A

because its wavefunction squared, so much always be positive

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16
Q

why is rdf more useful that wavefunction^2?

A

wavefunction^” doesn’t account for volume

17
Q

where can electrons not be found?

A

nodes - as wavefunction at nodes = 0

18
Q

what is the area under the rdf curve represent?

A

probability of finding 1 electron - no matter which orbital so when drawing many orbital wavefunctions on the graph, they must seem to have similar areas under the curve

19
Q

why does the maxima of the rdf curve shift to a larger r as QN n increases?

A

this is because the size of the orbital increases and it is at a higher energy level so its more likely that electrons are found further from the nucleus

20
Q

how does stability change as QN n increases?

A

stability decreases as orbitals become further form nucleus, so at higher energy levels
this means on an rdf graph, consecutive orbitals with different n values would start/be drawn higher on the yaxis

21
Q

is an electron more likely to be closer to the nucleus in a 2p or 2s orbital + why?

A

2s - looking at the rdf plots, although 2p is on average closer to nucleus judging by maxima, the 2s has a smaller peak at low r that penetrates the 2p, which gives it greater probability of being closer to the nucleus