ap chemistry topic review 2014
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AP Chemistry Topic Review 2014. Periodicity. Effective nuclear charge (Z) Generally speaking, effective nuclear charge is the charge felt by the valence electrons after you have taken into account the number of shielding electrons that surround the nucleus . 1 st level of a neon atom 10 - PowerPoint PPT PresentationTRANSCRIPT
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AP Chemistry Topic Review2014
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Effective nuclear charge (Z)Generally speaking, effective nuclear charge is the
charge felt by the valence electrons after you have taken into account the number of shielding electrons that surround the nucleus.
1st level of a neon atom 102nd level of a neon atom: 81st level of a sodium level: 112nd level of a sodium atom: 93rs level of a sodium atom: 1What about a sodium ion?
Periodicity
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Coulombs LawCoulomb's Law relates the magnitude and sign of the electrostatic force acting simultaneously on two point charges and as follows:F = (ke)q1q2
r2
where r is the separation distance and ke is Coulomb's constant. If the product q1q2 is positive, the force between the two charges is repulsive; if the product is negative, the force between them is attractive.
Compare NaCl to MgCl2
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VSEPR
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hybridization
sp3: 4 EQUAL sigma bonds
sp2: 3 sigma, 1 pi n sp2 hybridization the 2s orbital is mixed with only two of the three available 2p orbitals
sp: 1 sigma 2 pi
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Infrared spectroscopy deals with the interaction of infrared light with matter
E = hnwhere h = 6.6 x 10-34 joule second and n = frequency of the photon. This shows that high energy photons have high frequencyThe frequency, n, and speed of light, c, are related through the relation
c = nwhere c = 3.0 x 108 meter/second and l = wavelength for the lightMolecules are flexible, moving collections of atoms. The atoms in a molecule are constantly oscillating around average positions. Bond lengths and bond angles are continuously changing due to this vibration. A molecule absorbs infrared radiation when the vibration of the atoms in the molecule produces an oscillating electric field with the same frequency as the frequency of incident IR "light"
Spectroscopy
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The infrared spectrum for a molecule is a graphical display. It shows the frequencies of IR radiation absorbed and the % of the incident light that passes through the molecule without being absorbed. The spectrum has two regions. The fingerprint region is unique for a molecule and the functional group region is similar for molecules with the same functional groups.
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Concentration (M) Absorbances0.20 0.270.30 0.410.40 0.550.50 0.69
Beer’s Law (Colorimetry, Spectroscopy)The graphing method is called for when several sets of data involving STANDARD SOLUTIONS are available for concentration and absorbance. This is probably the most common way of Beer's law analysis based on experimental data collected in the laboratory.Graphing the data allows you to check the assumption that Beer's Law is valid by looking for a straight-line relationship for the data.Question: What is the concentration of a 1.00 cm (path length) sample that has an absorbance of 0.60?
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Beer’s LawA = εcl, where A is absorbance, c is concentration, l is cuvette width, and ε is the molar absorptivity of the molecule and I is intensity. If you have a set of solutions of known concentration, and you measured their absorbance, then plot A vs c, and the slope of this plot will be the molar absorbtivity ε (since l = 1). Then with ε, the concentration of a solution of this substance can be measured by measuring the absorbance.
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Spectral Ranges
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Classification
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Intermolecular forcesIonic bonding
Attraction between – and + ionsCovalent bonding and Polarity
Hydrogen “bonding” H- F,O,NDipole dipole forces: high en differenceLondon dispersion forces: get higher with
larger molecules
Unique properties of water
Molecular solids Vs. Ionic solids
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Metallic bonding constitutes the electrostatic attractive forces between the delocalized electrons, called conduction electrons, gathered in an electron cloud and the positively charged metal ions. Understood as the sharing of "free" electrons among a lattice of positively charged ions (cations), metallic bonding is sometimes compared with that of molten salts; however, this simplistic view holds true for very few metals. In a more quantum-mechanical view, the conduction electrons divide their density equally over all atoms that function as neutral (non-charged) entities. Metallic bonding accounts for many physical properties of metals, such as strength, ductility, thermal and electrical conductivity, opacity, and luster
Metals
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In a network solid there are no individual molecules and the entire crystal may be considered a macromolecule Examples of network solids include diamond with a continuous network of carbon atoms and silicon dioxide or quartz with a continuous three-dimensional network of SiO2 units. Graphite and the mica group of silicate minerals structurally consist of continuous two-dimensional layers covalently bonded within the layer with other bond types holding the layers together
Network Solids
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Stable, high-melting substances held together by STRONG electrostatic forces that exist between oppositely charged ions.
Ionic Solids
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Lewis Dot Structures and Polarity of a molecule
Molecules
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Solution processes
Polarity
Particulate level representation
Solutions
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Acid base
Precipitation reactions
Redox reactions
Solution stoichiometry
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KMT
Ideal gases
Ideal gas law
Phases of Matter
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Boyles
Charles
Combined
Daltons
Gas laws
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Graphs
Heating curvePhase diagram
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Critical Temperature: Temperature above which the vapor cannot be liquefied. Critical Pressure: Pressure required to liquefy AT the critical temperature. Critical Point: Critical temperatue and pressure (for water, Tc = 374° C and 218 atm).
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Physical vs chemical changes
Reaction review
Enthalpy
Activation energy
Physical and Chemical Processes
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Redox reactions and cell potential
Connections between cell potential and free energy
Redox titrations
Electrochemistry
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Particles must collide.Only two particles may collide at one time. Proper orientation of colliding molecules so that atoms can come in contact with each other to become products.
THE COLLISION THEORY OF REACTION RATES
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The basics
Example
Rate laws
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Rate laws
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Rate laws: A SUMMARY
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the slowest step is the rate determining step
reaction intermediate--produced in one step but consumed in another.
catalyst--goes in, comes out unharmed and DOES NOT show up in the final rxn.
Rate Mechanisms
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Rate Law Rate Determining Step in the mechanism Rate = k[A]
Rate = k [A][B]
A X (slow)
A + B X (slow)
Rate = k [A]2 A + A X (slow)
Rate = k [A]2[B]
A + A D X (fast)B + X Y (slow)Each step is usually bimolecular. A third order overall reaction often comes from a fast equilibrium before a slow step.
Rate = k This could be a mechanism that depends on a catalystonly. The concentrations would not matter.
Molecularity of the Rate Determining Step in the Mechanism
Elementary Step
Molecularity Rate Expression
A products unimolecular Rate = k[A]A + B products
bimolecular Rate = k[A][B]
A + A products
bimolecular Rate = k[A]2
2A + B products
termolecular Rate = k[A]2[B]
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ENERGY AND WORK
E = q(heat) + w(work)
Signs of q: +q if heat absorbed–q if heat released
w = -PVNOTE: Energy is a state function. (Work and
heat are not.)
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Signs of w (commonly related to work done by or to gases)
+ w if work done on the system (i.e., compression)-w if work done by the system (i.e., expansion)
When related to gases, work is a function of pressure (pressure is force per unit of area) and volume
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Calculate ∆E for a system undergoing an endothermic process in which 15.6 kJ of heat flows and where 1.4 kJ of work is done on the system.
∆E = 17.0 kJ
Exercise 1Internal Energy
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ENTHALPY
Measure only the change in enthalpy, H (the difference between the potential energies of the products and the reactants) H is a state function
H = q at constant pressure (i.e. atmospheric pressure)(true most of the time for us and a very handy fact!)Enthalpy can be calculated from several sources including:
Stoichiometry Calorimetry From tables of standard
values Hess’s Law Bond energies
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The process of measuring heat based on observing the temperature change when a body absorbs or discharges energy as heat.
After all data is collected (mass or volume; initial and final temperatures) we can use the specific heat formula to find the energy released or absorbed. We refer to this process as constant pressure calorimetry.
** q = H @ these conditions.**
Calorimetry
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Specific heat capacity (Cp)Confusing terms: Specific heat, specific heat capacity, molar heat capacity, latent heat
Heat capacity (C): the amount of energy per rise (or fall) in temperature. This is an intensive property and unique to each substance. The specific heat capacity of water is 1cal/C or 4.18J/ C
Energy released or gained: q = CmT Specific heat (S): Same as specific heat but specific to 1 gram of substance It is an extensive property. It’s units are J/g C
S= heat transferred(grams of material)(temp change)
Latent Heat: energy required for a phase change. Units are usually J/g
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K = [products] [reactants]Leave out pure liquids and solids
Kp = Kc(RT)n
K > 1 products favoredK < 1 reactants favored
Use RICE tables!
Equilibrium
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effect of changes in concentration, pressure, & temperature. Equilibrium always “shifts” away from what you add. “Stress” means too much or too little: chemical, heat, or room
Ex:
LeChatelier’s Principle
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Buffers are a mixture ofa weak acid & its conjugate base ora weak base & its conjugate acid.Examples:HC2H3O2 & C2H3O2-or NH3 & NH4
+
HA H+ + A- Ka = [H+][A-] [HA]
The best buffer, Ka = [H+]; pH = pKa.
The pH of a buffer can be adjusted by changing the ratio of acid and base.
Buffers
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Steps: Change volumes to moles using molaritySubtract the moles used from the reactants
and add moles gained by the productsChange moles back to molarity using the new
volumesWrite and use your RICE tableSolve for x
Example:
Titrations
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Solubility RulesReview/memorize these rules. They can be split into four groups: ALWAYS SOLUBLE:
alkali metal ions (Na+, K+, Li+, Rb+, Cs+), NH4+, NO3
-, C2H3O2-, ClO3
-, ClO4-
USUALLY SOLUBLE:
chlorides, bromides, iodides (Cl-, Br-, I-) except “AP/H” (Ag+, Pb2+, Hg22+)
sulfates (SO42-) except “CBS/PBS” (Ca2+, Ba2+, Sr2+, Pb2+)
fluorides (F-) except “CBS/PM” (Ca2+, Ba2+, Sr2+, Pb2+, Mg2+) USUALLY INSOLUBLE:
oxides/hydroxides (O2-, OH-) except “CBS” ((Ca2+, Ba2+, Sr2+) NEVER SOLUBLE:
CO32-, PO4
3-, S2-, SO32-, CrO4
2-, C2O42- except alkali metals & NH4
+
Solubility (Ksp)
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Example: Co(OH)2(s) Co2+ + 2OH-
Ksp = [Co2+][OH-]2 = 2.5 x 10-16
What is the pH of a saturated solution?Let x = the amount (moles) of solid that will just saturate 1 L of solution.
R Co(OH)2(s) Co2+ + 2OH-
I --- 0 0 C +x +2x E x 2x
(x) (2x)2 = 4x3 = 2.5 x 10-16
x = 3.97 x 10-6 [OH-] = 2x = 7.94 x 10-6
pOH = 5.1 pH = 14- pOH = 8.9
Ksp
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Will a Precipitate Form?Ion Product (Qsp) = “reaction quotient”.
Qsp < Ksp more solid will dissolveQsp = Ksp solution is saturatedQsp > Ksp ppt will form until Qsp = Ksp
Note: Be sure to calculate concentration of DILUTED ions. Example:50. mL of 2.0 x 10-4 M Co(NO3)2 is mixed with 200 mL of 1.0 x 10-3 M NaOH. Will a precipitate form?[Note:Ksp given in other example problem.] [Co2+] = 2.0 x 10-4 M x = 4.0 x 10-5 M[OH-] = 1.0 x 10-3 M x = 8.0 x 10-4 MQsp = (4 x 10-5) (8 x 10-4)2 = 2.56 x 10-11
Qsp > Ksp; a precipitate will form!
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Product or Reactant favored reactions depend on H, S, and absolute Temp
Thermodynamics
H S Product-Favored…
+ + at higher temperatures
- - at lower temperatures
- + at all temperatures
+ - never(reactant-favored at all temps)
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Gibbs Free Energy, G, puts the effects of H, S, and Temperature together.
G = H - TS
G<0, G -, product-favored reactionG>0, G +, reactant-favored reactionG=0, reaction is at equilibrium
Free Energy
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Balance half reactions:write two separate half-reactionsbalance all atoms except H & Obalance O’s (add H2O’s)balance H’s (add H+’s)add e- ‘s to more positive sidebalance e-‘s between half-reactionscombine half-reactionsadjust for basic solution if needed
Electrochemistry
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Every atom has a different “potential” to accept electrons… “reduction potential”The reduction with the more positive E value will occur as written; the other reaction will reverse (oxidation). Ex: 2Ag+ + Cd 2Ag + Cd2+
+0.80 v – (-0.40 v) = 1.20 voltsThe difference in the E values is the voltage of a cell made using these two reactions.
Oxidation occurs at the AnodeReduction occurs at the Cathode
Galvanic Cells
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coulomb (C) = an amount of chargeamp = current = charge per second1 amp · 1 second = 1 Coulomb1 C / amp·sFaraday constant, F:
1 mole e- = 96,500 CElectrolysis calculations begin with amp·s
Example:How many moles of copper metal can be plated using a 10 amp circuit for 30 s?10amp x 30s x 1C x 1 mol e- x 1 mol Ag = 1 amp·s 96500C 1 mol e-
= 3.1 x 10-3 mole Ag
Electrolytic Cells
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Organic ChemistryAlkanesSingle bonded C
AlkenesDouble bonded C
AlkyneTriple bonded C
MethaneEthanePropaneButanePentane
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Alkyl groups
Cis and trans
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Functional Groups
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Benzene
Aromatics (cyclics)
Meta and para