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Valence bond theory
electrons in a molecule occupy orbitals of the individual atoms, bonds form when unpaired electrons in the valence shell atomic orbitals pair
Orbital overlap
orbitals on two atoms overlap
Sigma bond
density concentrated along the intra-nuclear axis (between two nuclei)- hybrid orbitals and lone pairs
Hybrid orbitals
combination of wave function of the same atom to form a new set of equivalent wave functions; a combination of all orbitals of an atom
Pi bond
overlap of p orbitals oriented perpendicularly to the inter-nuclear axis (two separate regions of electron density)
sp hybrids
-2 ED
-linear
sp2 hybrids
-3 ED
-trigonal planar
sp3 hybrids
-4 ED
-tetrahedral
sp3d hybrids
-5 ED
-trigonal bi-pyramidal
sp3d2 hybrids
-6 ED
-octahedral
Molecular orbit (MO) theory
mathematical function that describes the behavior of an electron in a molecule (forms from the overlap of atomic orbitals)
constructive interference
-bonding (σ)
-stabilizing, lowers energy
-amplitude increases
destructive interference
-anti bonding (σ*)
-increases energy’
-no amplitude (flat line)
Bond order
how stable a molecule is (adding an electron to bonding MO increases the BO, adding an electron to an anti-bonding MO decreases the BO)
Paramagentic
unpaired electrons, strongly attracted to the magnetic field
Diamagnetic
all electrons are paired, slightly repelled by the magnetic field)
Bond order vs bond type
1= single bond
2= double bond
3= triple bond
*BO can be fractional*