Chemical bonds result from a more stable energy state. See page 356 (Fig 9.15)
Basic definitions:
ionic: e- transfer results in ions that are electrostatically attracted to each other (Lewis dot)
covalent: e- sharing (See page 305, Figure 8.5)
non-polar(even sharing), polar (uneven)
See page 309, Figure 8.7 & dipole moments on page 310
metallic: sea of valence electrons
Use periodic table position to predict bond type (metal & nonmetal = ionic, 2 metals = metallic, 2 nonmetals = covalent
Use electronegativities on page 308 to predict bond type
Percent ionic character (Difference in electronegativities / larger electronegativity)
0% - 5% (nonpolar)
5% - 50% (polar)
> 50% (ionic)
Sample 8.4 on page 309
Not all polar bonds result in polar molecules. (Example: CO2)
A closer look -
Ionic = e- transfer to Noble gas or pseudo noble gas structure
Crystal formation - see page 300 - So use empirical formula
Ions will dissolve in water and become "free"
Read about lattice energy (Sample 8.1)
Homework: Pg 333, #17, 19, 39
Localized Electron Bonding Model - see page 305
lone pairs, bonding pairs
Lewis Dot Structures for Molecular Compounds (File: WS DOT) (see Lewis Covalent.ppt)
Step 1: Calculate the number of electrons needed to fill all the atoms' valence shells.
Step 2: Count valence electrons (Add electrons for negative ions and subtract electrons for positive ions)
Step 3: Subtract to find number of shared electrons.
Step 4: If > 2 atoms, select central atom. (Usually C or atom with lowest electronegativity.)
Step 5: Arrange other atoms around central atom.
Step 6: Draw in shared electrons.
Step 7: Draw in unshared electrons.
Step 8: Check: Count for total valence electrons and check each atoms individual structure.
Examples: NH3, H2S, CO2, HCN, NBr3, SO32- and NH4+
Homework: Page 335, #45, 49 (no formal charge)
Bond length and bond strength: More electrons being shared = shorter and stronger
Resonance: Page 319. Two or more Lewis structures: Real = average. Sample 8.10 (p 320)
Homework: Page 335, #51ac, 53, 55
Exceptions to octet rule (page 322)
a. Odd number of electrons (NO)
b. Less than octet: BF3
Coordinate bonding - one atom donates both of the shared e-'s
BF3 + NH3 ® nitrogen donates (w/boron)
c. More electrons than octet (Period 3 and beyond - big enough to have d orbitals to use.)
PCl5 & ICl4- (Sample 8.11)
Homework: Page 335, #61
Hybrid orbitals: sp on pg 358 dsp3 on pg 361
sp2 on pg 359 d2sp3 on pg 361
sp3 on pg 359 review on pg 361
VSEPR - valence shell electron pair repulsion (starts on 344) - structure is determined by minimizing electron pair repulsion.
See rules on page 346 and shape-names/pictures on page 347 and 350
Note: lone pairs - require more space. (shared pairs confined by two nuclei)
Figure 9.7 on page 348 OR all e-, no p+ ® more repulsion
Use H2O (109.5o), NH3 (107o), CH4 (105o) transparency
Resonance - any structure can be used to predict geometry
Multiple bonds - act as a single shared pair (Count zones of e-)
See pictures & problems page 396-403
Homework: Pg 384 #17 – 35 odd, 47
Molecular orbitals – not tested in AP except for one small part.
Two kinds –
Sigma – overlap of orbitals that extend towards each other, between the nuclei
Figure 9.14 on page 356, Figure 9.17 on page 358
Pi – orbitals lined up side by side and overlapping in two regions
Figure 9.22 on page 362 through Figure 9.27 on page 364
Single bond = sigma
Double bond = sigma and pi
Triple bond = sigma and two pi
Note: resonance = delocalized pi bonding of unhybridized p-orbitals
See pages 365 & 366
General Conclusions on page 368
Homework: Page 386, #51a-d, 53
So far three kinds of bonding - ionic, metallic, covalent. These are intramolecular forces.
Now look at intermolecular forces (van der Waals attractions). Chapter 11, section 2
1. dipole-dipole attraction (positive end of one polar molecule is electrostatically attracted to the negative end of another polar molecule) See picture page 439 and 440
2. hydrogen bonding - a special dipole-dipole attraction
H to F,O,N. About 5 - 10% strength of regular covalent bond.
3. London dispersion forces: (See picture on pg 441) "induce dipole"
(-v- permanent dipole of polar molecules)
Strength of forces increases with atom/molecule size
larger molecules = more e-'s (farther from pull of own nucleus/electron shielding) = more London forces (I2 > F2)
The stronger the forces, the higher the melting points, boiling points, heat of vaporization, surface tension, viscosity, vapor pressure, etc.
Highest to lowest mp,bp,etc: ionics, hydrogen bonding, dipole-dipole, London dispersion
Note: LD is not the weakest. It’s just that H-bond and dipole-dipole is in addition to the LD that’s in all types of matter (because they all have electrons)
Relation to state of matter -v- molecular size (In class: see chart with bp of different substances)
metals - "giant electron cloud" or "sea of valence electrons": melting point, etc, raises with unpaired electrons through d's - highest in the middle of transition elements, then falls towards Zn column and rises through p orbital again (but not as high as mid‑d's)
Types of Solids: See Table 11.7 on page 464
Homework: Pg 472, #15, 19, 23, 25, 29, 31, 43, 45, 71-77 odd
and AP Worksheet - Atomic Theory and Worksheet - Bonding