# CC11. Solutions to Problems, CC1-CC4

#### CC11. Solutions to Selected Problems

##### Problem CC2.2.

a)   K = K1 x K2 x K3 x K4 x K5 x K6

=  470 x 130 x 41 x 12 x 4.2 x 0.81

= 1.03 x 108

b)  As the nickel binds ammonia  ligands, it becomes more electronically saturated.  That means it becomes less Lewis acidic.  It does not have as strong an attraction for additional ligands.

##### Problem CC2.3.
1. This is a Zn2+ ion binding to either NH3 or CN- ligands.  The zinc cation is more strongly sttracted to the anionic cyanide ligands than the neutral ammonia ligand, so the binding constant with cyanide is higher than with ammonia.
2. Both cases involve cyanide ions.  In one case, the CN- binds to Fe2+, whereas the other case involves Fe3+.  The ligand is more attracted to the more highly charged ion, so the binding constant is higher.
##### Problem CC3.4.

a)  Metal valence count:  9

Metal with charge:  6

Donated by ligands:  6 x 2 = 12

Total: 18

b)  Metal valence count:  8

Metal with charge:  5

Donated by ligands:  6 x 2 = 12

Total: 17

c)  Metal valence count:  9

Metal with charge: 7

Donated by ligands:  6 x 2 = 12

Total: 19

d)  Metal valence count:  7

Metal with charge:  0

Donated by ligands:  4 x 4 = 16

Total: 16

e)  Metal valence count:  8

Metal with charge: 8

Donated by ligands:  5 x 2 = 10

Total: 18

f)  Metal valence count:  10

Metal with charge: 6

Donated by ligands:  6 x 2 = 12

Total: 18

g)  Metal valence count:  6

Metal with charge: 6

Donated by ligands:  6 x 2 = 12

Total: 18

h)  Metal valence count:  6

Metal with charge: 0

Donated by ligands:  4 x 4 = 16

Total: 16

i)  Metal valence count:  9

Metal with charge: 8

Donated by ligands:  4 x 2 = 8

Total: 16

j)  Metal valence count:  8

Metal with charge: 4

Donated by ligands:  3 x 4 = 12

Total: 16

k)  Metal valence count:  9

Metal with charge: 7

Donated by ligands:  4 x 2 = 8

Total: 15

##### Problem CC3.5.

a)  6    b)  8    c)  5    d)  5    e)  10    f)  1    g)  10    h)  12    i)  2    j)  9    k)  4

a)  Metal valence count:  5

Metal with charge: 0

Donated by ligands:  5 x 2 = 10

Total: 10

b)  Metal valence count:  8

Metal with charge: 5

Donated by ligands:  3 x 2 = 6

Total: 11

c)  Metal valence count:  6

Metal with charge: 0

Donated by ligands:  6 x 2 = 12

Total: 12

##### Problem CC3.8.

a)  PF3 (104 vs 870)

b)  PMe3 (118 vs 870)

c)  PtBu3 (182 vs 1180)

d)  PtBu3 (182 vs 1450)

##### Problem CC4.6.

Zr(IV) or Zr4+ has no valence d electrons. That means that, although an alkene could certainly donate its pi bond to the zirconium atom, the zirconium has no electrons with which it can stabilize the alkene complex via "back-donation" to the pi antibonding orbital on the alkene.

Nevertheless, d0 metals such as Zr(IV) and Ti(IV) can be used as alkene polymerization catalysts to make common plastics such as HDPE, LDPE and polypropylene. That means that, although an alkene complex isn't directly observed with these metal ions, these metals can evidently bind alkenes briefly and get them to react with other alkenes to form long chains.  Even so, most industrial olefin polymerization catalysts use Ti(III).

##### Problem CC4.8.

We will use (a), the binding constant between Ag(I) and ethylene or ethene (CH2=CH2), as our baseline value.  Other constants will be compared with this one in order to look for a trend.

In (b), the binding constant is much smaller, so the silver ion binds cis-2-hexene much less tightly than it does ethene.  This is just another alkene, like ethene, but instead of having just hydrogen atoms attached to the C=C unit, cis-2-hexene has some other stuff.  Maybe this other stuff causes some problem for alkene binding.  The obvious difference between hydrogen atoms and this other stuff is that this other stuff is bigger.  Maybe the complex gets too crowded when the cis-2-hexene  binds to the silver ion.

Very often when we see metal ions on paper, we are not dealing with bare metal ions in reality.  The ion often has other ligands already attached to it at the beginning, such as water molecules, and what we are sometimes looking at is replacement of an old ligand with a new ligand. Other ligands attached to the silver could make crowding problems even worse.

There is an alternative explanation as well.  If you compare two alkenes that differ only in the number of hydrogens attached to the double bond, such as 1-butene, CH2=CHCH2CH3, and 2-butene, CH3CH=CHCH3, you invariably find that the alkene with fewer hydrogens attached to the double bond (and more other stuff) is more stable. "Terminal alkenes", with double bonds at the ends of the chain, are always less stable than "internal alkenes", with double bonds somewhere along the middle of the chain.  This difference can be explained by looking at some quantum mechanical calculations, but we're not going to do that right now.

The point is, the difference in this reaction might be caused, not by the alkene complexes, but by the alkenes themselves, on the other side of the reaction profile.  It's important to remember that equilibrium constants always compare two sides of a reaction. Ethene, having fewer substituents on the double bond than cis-2-hexene ("substituents" is a four syllable word for "other stuff"), may simply be less stable and more reactive.

Do either of these ideas hold up in the other examples?

In (c), trans-2-hexene is bound even less tightly than cis-2-hexene. We could argue that in a cis-2-hexene complex, the substituents, which are on the same side of the double bond, might both be held away from other ligands on the metal that may exacerbate crowding problems.  That would be more difficult to do with trans-2-hexene, since one substituent is on either side of the double bond.  Getting one substituent away from the crowding may be possible, but probably not both.

Once again, the alternative explanation holds up here, too. cis-2-Hexene is less stable than trans-2-hexene, because the substituents on the double bond crowd each other in cis-2-hexene, but are held away from each other in trans-2-hexene.  So maybe cis-2-hexene binds to silver ion more easily because it is more reactive.