AP Chem Ch 10 Flashcards
Exceptions to octet rule
B, Be, and Al (as a non-metal) are stable with 6 or 4 electrons
N is often stable with 7 electrons
P and larger atoms are often stable with 10 or 12 electrons
Method for Lewis Dot Structure
- Add up valence electrons
- Re count valence electrons
- Arrange atoms. Least electronegative atom in the center
- Use pairs of electrons to draw in single bonds
- Put the rest of the electrons on the non central atoms trying to form octets
- Put extra electrons on central atom
- Check if central atom has octet
- Form double/triple bonds to give central atom an octet
Formal charge
valence e- - #bonded electrons/2 - # of electrons in a lone pair
Ex. Oxygen in a double bond:
6-4/2-4
London dispersion forces
Induced/temporary dipole
Increases with size–larger the molecule, bigger the LDF
Type of IMF for non-polar molecules
As you go down a group, freezing and boiling points increase because bigger LDF. Stronger IMF allows for this increase
Polarizability
The freezing point rises going down the group. Principle reason for this is because as the atomic number goes up, number of electrons GO up, so there is an increased chance of the occurrence of momentary dipole interactions. We describe this phenomenon using the term polarizability, which indicates the ease with which the electron cloud of an atom can be distorted to give a dipolar charge distribution. Thus we say that large atoms with many electrons exhibit a higher polarizability than small atoms. So, LDF increases as size increases
Dipole-Dipole
Molecules with a permanent dipole (polar species) desire to align to reduce repulsions. More favorable–less energy required–when a polar molecule interacts with another polar molecule.
H-bonding
Extreme case of dipole-dipole where Hydrogen is attracted to a lone pair in an N, O, or F atom.
Very strong IMF because of the big electronegativity difference–strong polar bond between H-N, H-O, H-F
Also occurs because the dipoles are able to closely approach one another because hydrogen is so small.
Effects of hydrogen bonding
Since the IMF is so strong, higher boiling and melting points, less vapor pressure than dipole-dipole or LDF species
Why do polar molecules mix with polar molecules and not with non-polar molecules?
Polar– dipole produced with a partial positive and a partial negative side. Attracted to other polar molecules where partial positive is attracted to partial negative because this is a favorable reaction, can just bond, doesn’t take too much energy
However, this partially charged molecule won’t interact with a non-charged non-polar molecule unless a lot of energy is induced, so this is not favorable
Surface tension
The resistance of a liquid to an increase in its surface area. Liquids with large IMFS have high surface tension.
Capillary action
Spontaneous rising of a liquid in a narrow tube.
Caused by 2 different types of forces:
1. Cohesive forces– IMF among the molecules of the liquid
2. Adhesive forces– forces between liquid and container
Adhesive forces occur when the container is made of a substance with polar bonds so the water can attract to it.
The ability of water to wet the glass makes it creep up the walls of the tube where the water surface touches the glass. Increases the surface area of the water, which is opposed by the cohesive forces trying to minimize the surface. So, with the strong adhesive and cohesive forces, water pulls itself up a glass capillary tube to a height where the weight of the column of water just balances the water’s tendency to be attracted to the glass surface.
Cohesive vs adhesive forces
Cohesive among molecules of a liquid
Adhesive with liquid and the container
Concave vs convex meniscus and reason why
Polar has a concave meniscus because of strong adhesive forces.
Attracted to the glass
Nonpolar is convex because of strong cohesive forces. Won’t interact with the polar glass tube.
Viscosity
Measure of the resistance to flow.
Larger IMFS have larger viscosities
Also more sticky with higher viscoscities
Solid vs gas vs liquid
Solid is rigid structures with essentially no molecular motions
Gas has lots of motion. No IMFs
Liquid the hardest to analyze because of both motion and IMFS
X - ray diffraction
Diffraction occurs when beams of light are scattered from a regular array of points in which the spacing between the components are comparable with the wavelength of the light.
Allows for structure of crystalline solid to be determined
Constructive vs destructive interference
Constructive when the waves of parallel beams are in phase. Produces a spot on the detector
Destructive when the waves are out of phase. No image produced.
Importance of diffraction
Allows for bond lengths to be determined from the Bragg eq
Bragg equation
n (lambda) = 2d * sin (theta) n is an integer Lambda is the wavelength d is the disfrace between points Theta is the angle of incident light
Example of Bragg equation
If the wavelength of an Al crystal is 1.54 * 10^-10 m and it produces reflection at an angle of 19.3 degrees and we assume n=1, calculate the distance between the planes of atoms producing this reflection
Use Bragg equation:
1(1.54*10^-10)=2dsin(19.3)
d = 2.33 * 10^-10 m
Molecular orbital theory for metals
Bonding in most metals is both strong and nondirectional because they are durable and have high melting points.
Electron sea model explains how there is a regular array of metal cations in a sea of valence electrons. Mobile electrons can conduct heat and electricity and the metal ions can be easily moved around as the metal is hammered into a sheet or pulled into a wire
A related model with more detailed view of the electron energies and motions is the band model, or molecular orbital model, for metals. In this model, the electrons are assumed to travel around the metal crystal in molecular orbitals formed from the valence atomic orbitals of the metal atoms. Large number of resulting molecular orbitals are closely spaced and finally form a virtual continuum of levels, called bands.
How does temperature affect conductivity of a metal?
T up, so more collisions, so less conductivity.
Band theory to explain metals conducting
Conduct electricity and heat very efficiently because of the availability of highly mobile electrons. Electrons in partially filled bonds are mobile, so they can flow and create charge. The molecular orbitals occupied by these conducting electrons are called conduction bands. These account for the efficiency of the conduction of heat thru metals. When one end of a metal rod is heated, the mobile electrons can rapidly transmit the thermal energy to the other end.
Which has a bigger gap between conductive and valence band?
Insulator bigger gap than semiconductor
Closest packing
The structure in crystalline solid materials. Packing uniform hard spheres in a manner that most efficiently uses the available space.
Aba arrangement
Hexagonal closest packed (hcp) – hexagonal unit cell. Third layer lies directly over the first because of dimples between first and second, and second and third layers.
ABC arrangement
Cubic closest packed (ccp) structure. Face centered cubic unit cell. Fourth layer is like the first. Abcabc
FCC has 4 atoms in 1 unit cell.
And one side you can do by the diagnaol, and then pi that, so d^2 + d^2 = (4r)^2
Simple cubic, body-centered cubic, face centered cubic
SC– 1 atom per unit cell. 2r= one side
BCC– 2 atoms in a unit cell.
FCC– 4 atoms in a unit cell. One side = 4r/SQRT2
Ex. Silver crystallizes in a CCP structure. Radius is 144 pm
Find the density of solid silver
CCP structure, so 4 atoms in a unit, so (4r)^2 = d^2 + d^2
d = 144SQRT 8 = 407 pm
Volume = side cubed = 6.7410^7 pm^3 * 1/10^30 cm^3 = 6.7410^-23 cm^3
Mass–we know that there are four atoms–> 107.9 g/mol * 1 mol/6.0210^23 afoms * 4 afoms = 7.17*10^-22 g
Mass / volume = 10.6 grams per cubic cm
Substitutional alloy
When a metal has equal in size secondary metal.
Host atoms are replaced by other metal atoms of similar size
Brass, sterling silver
Interstitial alloy
Some holes in the closest packed metal structure are occupied by small atoms, most of the time, carbon. Changes properties and makes it stronger
Network solids
Many atomic solids contain strong directional covalent bonds to form a solid that might best be viewed as a giant molecule.
Brittle, do not efficiently conduct heat or electricity.
Carbon– diamond, graphite
Silicon– silicates, silica
Big networks of Si and O
Ionic solids
Metal and nonmetal Ionic bonds Latrice High boiling and melting points because of high electrostatic attraction Very soluble in aqueous solution