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l = 0 corresponds to the 1s orbital – an s orbital has no
angular nodes
l = 0 corresponds to the 2s orbital – still no
angular nodes, has 1 radial node
l = 1 corresponds to the 2p orbitals – a p-orbital has
one angular node, no radial nodes
l = 0 corresponds to the 3s orbital – still no
angular nodes
l = 1 corresponds to the 3p orbitals – a p-orbital has
one angular node, 1 radial node
l = 2 corresponds to the 3d orbitals – a d-orbital has
two angular nodes
Removing electrons leads to an increase in
Zeff (less shielding) so metal cations have smaller ionic radii than the neutral metals
Adding electrons leads to more shielding (larger Zeff) and anions have larger
•ionic radii than neutral atoms.
As Zeff increases across a group then (the magnitude of) the
electron affinity increases.
As Zeff decreases down a group then (the magnitude of) the electron affinity
decreases
AX3
trigonal planar’
AX2E
‘angular’ (or ‘bent’)
AX4
tetrahedral
AX3E
trigonal pyramidal’
AX2E2
angular
AX5
‘trigonal bipyramidal’
AX4E
see-saw’
AX3E2
T-shaped’
AX6
‘octahedral’
AX5E
‘square-based pyramid’
AX3E3
‘T-shaped’
AX4E2
square planar
AX2E3
linear’
A or B
singly degenerate’ representation labels
E
•doubly degenerate’
T
•‘triply degenerate’
on descending the group, the s-p separation increases and it becomes increasingly harder to promote the
electrons to become involved in bonding – inert pair effect.
Fluorine is sufficiently strong oxidizer to form the group oxidation state (+6), but chlorine can only achieve
+4 (reflecting inert nature of the lone pair)
On descending the group s-p separation increases – promotion energy gets larger – the lone pair has more s-character and
p-orbitals are primarily used in bonding... bond angles get closer to 90o on descending the group
Steric effects – bond angle increases to
accommodate larger size of Cl and then
Br