I got this during a Princeton Review passage earlier today. I kind of understand it, but then I got this:
Bond order is defined by the expression 1/2(# of bonding electrons – # of anti-bonding electrons)
A bond order of zero indicates an unstable molecule or ion. A higher bond order means a shorter bond length and a greater bond dissociation energy. If a molecule has unpaired electrons, then it is paramagnetic, as opposed to diamagnetic.
An ion of O2 2+ would be predicted by this theory to have a bond order of:
A bond order of zero indicates an unstable molecule or ion. A higher bond order means a shorter bond length and a greater bond dissociation energy. If a molecule has unpaired electrons, then it is paramagnetic, as opposed to diamagnetic.
An ion of O2 2+ would be predicted by this theory to have a bond order of:
So, O2(2+) = 8*2 -2 = 14 electrons.
So, going up: if each orbital is 2 electrons...I got 4? But the answer is no, bond order is 3.
Therefore (filling orbitals from bottom to top), the s1s, s*1s,s2s, s*2s, p2p, and s2p orbitals would be filled.
How does this even work?! What is going on!!
How does this even work?! What is going on!!
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