Zeff for O is greater than for C, so we expect the atomic orbitals of O to be lower in energy than those of C.
The 2s and 2pz orbitals are σ-type, and the 2px and 2py orbitals are π-type.
It is more important to interpret the MO diagram rather than try to predict it from scratch.
They result from sideways overlap of the px and py orbitals, as usual.
There is significant s-p mixing in the σ-bonding network of CO.
From calculations, specifically noted as density functional theory.
Because there is enough s-p mixing that the σ orbitals are better treated as a sequence of mixed σ orbitals rather than as pure 2s- or 2p-derived orbitals.
Each C–O σ molecular orbital has mixed s and p character.
They can contain bonding, nonbonding, and antibonding contributions.
Do not worry too much about deriving it by hand; calculations sort it out, and your job is to interpret the diagram.
1σ is largely bonding with large contributions from O atomic orbitals.
2σ is more bonding than antibonding.
3σ is more antibonding than bonding.
4σ is extremely antibonding.
Because significant s-p mixing makes the simple bonding-minus-antibonding counting less straightforward.
The HOMO is the 3σ orbital.
It has a lot of p character and more C character than O character.
Because it is closer in energy and character to the carbon atomic orbitals and is concentrated more on C.
The LUMO is the π*(2p) orbital.
It has more carbon character than oxygen character.
Because incoming electron density or back-bonding into the LUMO will be directed into an orbital with strong carbon-side contribution.
Ask whether the latest and appropriate models were used, whether the model matches your actual system, whether solvent and reaction conditions were included, whether the calculation treats ΔG or only ΔH, and whether results were compared to real measured values.
Highest Energy Occupied Molecular Orbital.
Lowest Energy Unoccupied Molecular Orbital.
Usually the HOMO and the LUMO.
From the HOMO.
Because it is the highest-energy occupied orbital, so those electrons are easiest to give up.
Into the LUMO.
Because it is the lowest-energy empty orbital available.
Absorption of a photon that promotes an electron from the HOMO to the LUMO.
The energy of the absorbed photon.
Their energies, shapes, and locations generally determine much of the chemistry of the molecule.
By σ donation from the carbon lone-pair-like HOMO into an empty σ orbital on Fe and π back-bonding from filled Fe dπ orbitals into the π* LUMO on CO.
An empty σ orbital on Fe, described as a blend such as s, pz, and dz2 character.
The lone pair on carbon in the 3σ HOMO.
The π* orbital on CO, which is the LUMO.
Synergistic bonding.
Because the σ donation and π back-bonding work together synergistically.
Because synergistic bonding of CO to Fe is stronger than Fe–O2 bonding in blood, so CO blocks O2 from binding to Fe.
CO is odourless, colourless, and deadly, so you must be trained and follow every safety procedure.
Using Lewis structures, VSEPR, and hybridization.
sp3.
The valence atomic orbitals are the 2s and 2px, 2py, 2pz orbitals.
Calculations show no s-p mixing.
CO has significant s-p mixing in its σ network, but methane does not according to the notes.
You need calculations to solve MO energy level diagrams with precision.
Interpret the MO energy level diagram after the calculations are verified.
Shapes, geometries, and symmetry, especially of the HOMO and LUMO.
They determine how a molecule accepts electrons.
BF3.
The B–F σ* orbital and an unhybridized 2pz orbital.
The 2pz orbital on boron.
Because it can accept electrons into the empty 2pz orbital.
They determine how a molecule gives up electrons.
Absorbing light promotes an electron from the HOMO to the LUMO.
ELUMO − EHOMO.
S1 and T1.
Intersystem crossing.
The 2s orbital on carbon bonds with four H 1s orbitals, or portions thereof.
One σ bonding molecular orbital smeared out over five atoms.
A corresponding antibonding MO spread over the C and H framework.
Carbon p orbitals also combine with H 1s orbitals to form bonding molecular orbitals.
They are shown in the plane of the page for visualization.
That molecular orbitals can extend over the whole molecule rather than being localized as simple single bonds.
They are the d-block metals.
They use s, p, and d valence orbitals.
s, p, dx2−y2, and dz2.
dxy, dxz, and dyz.
Because transition metals can use many different valence orbitals and bonding modes.
s-block elements have low electronegativity and low Zeff and tend to donate electrons, while p-block elements tend to have higher Zeff and can accept electrons to complete a valence shell.
They are electron donors and can make metal ions such as M2+.
They can make covalent bonds, like CH4, or accept electrons, like in ionic compounds such as Na+Cl−.
The elemental form electron configuration of the neutral atom.
The nd orbital is always lower in energy than the (n+1)s orbital.
Because when forming transition-metal ions and complexes, electrons are removed from the (n+1)s before the nd set.
Octahedral, an ML6 compound.
A ligand, meaning a molecule or atom bonded to the transition metal.
[Ar]4s2 3d7.
[Ar]3d7.
Because in complexes the 3d orbitals are lower in energy than 4s, so the 4s electrons are removed first.
V2+ and Cr3+ often have the same chemistry because both can give d3 configurations.
Ta2+ can be [Xe]5d3.
Cr is [Ar]4s1 3d5 and Cu is [Ar]4s1 3d10.
Most Cu complexes are Cu(I) d10 or Cu(II) d9.
Metallic bonding.
They are metallic.
[Ar]4s1 3d10.
[Ar]4s2 3d8.
For complexes and cations, nd ends up lower than (n+1)s, so remove s electrons first.
HOMO donates, LUMO accepts.
CO donates from carbon through its HOMO and accepts back-bonding into its π* LUMO, giving strong synergistic bonding.
It binds Fe more strongly than O2 does and blocks oxygen binding.
Hybridization is useful and intuitive, but the real MO picture uses C 2s and 2p orbitals spread over the whole molecule.
