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N330 Terms Midterm 2

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bronsted acid
a proton donor
Bronsted base
a proton acceptor
4 things that dictate coordination number
1. size of central atom 2. steric interactions between ligands 3. electronic interations - # of d electrons on metal, and if ligand can form multiple bonds 4. Charge - low valence = low coordination #
electrophile
electron pair acceptor AKA lewis acid!!!
Neucleophiles
ligands AKA lewis bases!!!
strong base
- virtually fully protonated in water -Example is the oxide ion (O2-) which is immediately converted to OH- ions in water.
polyprotic acid
a substance that can donate more than one proton. (H2S for example) in 2 successive proton donations it becomes S2- In these two deprotonations, the second Ka is always smaller than the first. This is becasue the proton becomes increasing harder to remove
Basicity Constant
Kb - if Kb is alot less than 1, then only a small fraction of B molecules are protonated, therefor, the base is a weak proton acceptor and its CA is present in low concentrations.
Acidity Constant
If Ka is alot less than 1, then the proton retention is favored by the acid.
Autoprotolysis constant
The constant involved when the proton transfer from one water molecule to another occurs.
3 classes of bronsted acids
aqua acids hydroxoacids oxoacids
aqua acids
an acid in which the acidic proton is on a water molecule coordinated to a central metal ion.
hydroxoacid
an acid in which the acidic proton is on a hydroxyl group without a neighbouring oxo group (=O)
Oxoacid
an acid in which the acidic proton is on a hydroxyl group with an oxo group attached to the same atom.
Periodic trend of aqua acid strength
increase with increasing positive charge of the central metal ion and with decreasing ionic radius
equation for determining pka of oxoacids
pka = 8-5p (p= # of oxo groups)
Conjugate base
a species with one or fewer protons than its parent acid
Conjugate acid
a species with one or more protons that its parent base
paulings rule
1) for oxoacid pka = 8-5p (OpE(OH)q) 2)The successive pka values of polyprotic acids (those with q>1), increase by 5 units for each proton transfer
amphoteric oxide
is an oxide that reacts with both acids and bases.
oxidation state for amphoteric Sc:
none, basic at 3+ and that is all
oxidation state for amphoteric Ti
4+, nothing higher (Acidic)
oxidation state for amphoteric V
4+
oxidation state for amphoteric Cr:
4+
oxidation state for amphoteric Mn
4+
oxidation state for amphoteric Fe:
3+ and 4+
oxidation state for amphoteric Co
3+
oxidation state for amphoteric Ni
3+
oxidation state for amphoteric Cu
2+
oxidation state for amphoteric Zn
2+
elements that have amphoteric oxides in all oxidation states
Be, Al, Ga, Ge, In, Sn, Pb
Elements that have acidic oxides in high ox states and basic oxides in low ox states
As, Sb, Bi
Lewis acid
electron pair acceptor
Lewis Base
electron pair donor
4 possibilities with lewis acids
1)incomplete octet can accept electron pair 2)metal cations bind ligands with lone pairs 3)complete octet rearranges to react with lone pair 4)molecule can accept electron pair to expand octet
ligand
an ion or molecule that can have an independent existence
A complex is:
a combination of a lewis acid (the central metal atom) with a number of lewis bases (ligands) bound.
Tetrahedral (coordination #)
4 - tetraheral complexes are favored over higher numbers when the central atom is small or the ligands are big because then the ligand-ligand repulsions override the energy advantage of forming more metal-ligand bonds.
square planar (coordination)
4 - are typically observed for metals with 8 d electrons.
common structure of 5-coordination complexes
square pyramidal and trigonal bipyramidal
common 6-coordination
octahedral
2-coordination complexes are common in:
groups 11 & 12 - typical for bottom right part of transition metals
Which 4-coordination complex has possible isomers and what are they?
square planar & cis and trans cis - like ligands are next to eachother trans - like ligands are opposite.
ambidentate ligands
ligands that have more than one different potential donor atom (ex. -NCS and -SCN)
chelate
a complex in which a ligand forms a ring that includes the metal atom. Binds to metal at two separate sites with 2 separate lone pairs.
chiral compound
non-superimposible on its mirror image.

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