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6. Give the definitions of the following terms:

Ionization energy, electropositive element, electron affinity, electronegative element, ionic bonding, Lewis structures, "Kekule" struc­tures.

Speaking

1. Alphabet dialogue. You are given the beginning of the sentences. Look at Appendix 1-2 and make up a dialogue without changing the order of these sentences. Speak about Molecular orbital theory and hybridization. You may use the following words and word combinations: an overlapping of atomic orbitals, to join together, arrangement of electrons, bond strength, to share the bonding electrons, bond length, bonding MO, antibonding MO, sigma bonds, principle of maximum orbital overlap, pi bond, unpaired electrons, excited-state configuration, electronic configuration, mix or hybridize, sp3hybridization, overlap head-on,sphybrid orbitals.

A- Ahh, anyway

B- But

C- Come to think of it

D- Doesn’t that mean…?

E- Errr

F- Fine, but…

G- Good point.

H- Hmmm…

I- I’d say…

J- Just a minute…

L- Let me see,

M – Mmmmm

N – Now, as I was saying…

O – Oh, but…

P – Put another way…

R – Right…

S – So…

T – Talking about….

U – Ummm

V – Very interesting, but…

W – Well…

Y – Yes, I know but…

2. Look at Appendix 3 and Render the following text.

We saw in ammonia that nonbonding lone-pair electrons can occupy hybrid orbitals just as bonding electron pairs can. The same phenomenon is seen again in the structure of water, H20. Ground-state oxygen has the electronic configuration ls22s22p%2py2pz, and oxygen is therefore divalent; that is, it forms two bonds.

We can imagine several hypothetical models for the bonding in water:

  1. Perhaps oxygen uses two unhybridizedp orbitals to overlap with hydrogen 1s orbitals. The two oxygen lone pairs would then remain in a 2s and a 2pxorbital.

  2. Perhaps oxygen undergoes sphybridization and uses the two sphybrid orbitals for bonding. The lone pairs would then both remain in the two unhybridizedp orbitals.

  3. Perhaps oxygen undergoes sp3hybridization and uses two sp3hybrid orbitals for bonding. The lone pairs would then occupy the remaining two sp3orbitals.

Only the third model, the hybridization of oxygen into sp3orbitals, allows strong bonds and maximum distance between the outer-shell electrons. The oxygen in water is therefore sp3hybridized.

Measurements on water indicate that the oxygen doesn't have perfect sp3hybrid orbitals; the actual H-O-H bond angle of 104.5° is somewhat less than the predicted tetrahedral angle. We can explain this bond angle difference by assuming that there is a repulsive interaction between the two lone pairs that forces them apart and thus compresses the H-O-H angle.

One final example of orbital hybridization that we'll consider is found in molecules like boron trifluoride, BF3. Since boron has only three outer-shell electrons (ls22s22px), it can form a maximum of three bonds. Even though we can promote a 2s electron into a 2pyorbital and then hybridize in some manner, there is no way to complete a stable outer-shell electron octet for boron.

Since boron has no lone-pair electrons to take into account, we might predict that it will hybridize in such a way that the three В—F bonds will be as far away from one another as possible. This prediction implies sp2 hybridization and a planar structure for BF3 in which each fluorine bonds to a boron sp2orbital, with the remaining p orbital on boron left vacant. Boron trifluoride has exactly this predicted structure.

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