Gen Chem MCAT – Flashcards
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Unlock answersatomic number |
number of protons and electrons in an atom (Z) |
mass number |
number of protons plus neutrons (A) |
Avogadro's number |
6.022 x 1023 particles |
Isotopes |
|
Quantum theory |
energy comes in discrete bundles |
Planck's constant |
h = 6.626 x 10 -34 Js |
angular momentum of an electron |
nh/2∏ |
Rydberg constant |
RH = 2.18 x 10 -18 J/electron
E = -RH/n2 |
Relate the energy level of an electron with the orbital radius |
Smaller radius = lower energy state |
Quanta |
Discrete energy bundle
E = hν |
Emission |
E = hc/λ
Emission gives rise to fluorescence |
Atomic emission spectra |
Unique for each element
E = -RH ((1/ni)2 - (1/(nf)2) |
Heisenberg Uncertainty Principle |
cannot determine precise momentum and position of an electron simultaneously |
Pauli Exclusion Principle |
no two electrons can have the same four quantum numbers |
principle quantum number |
n: describes size |
angular quantum number |
l describes shape, ranges from 0 to n-1 |
ml |
describes orientation, ranges from -l to l |
Hund's rule |
electrons prefer to fill empty orbitals before pairing (within same energy level) |
Paramagnetic |
has unpaired electrons, is attracted by magnetic field |
Diamagnetic |
have no unpaired electrons; repelled by magnetic field |
Valence electrons |
outer electrons that are most available for bonding |
Atomic radius |
|
Ionization energy |
|
Electronegativity |
|
electron affinity |
energy change that occurs when an electron is added to a gaseous atom ; (highest in halogens, zero in noble gases) |
Exceptions to the octet rule |
|
bond length |
decreases as number of bonds increases ; distance between two bonded atoms |
bond energy |
increases as number of bonds increases ; energy required to break a bond |
formal charge |
valence electrons - 1/2bonding - nonbonding ; sum of charges is charge on ion ; less charges on structure means it is more stable |
molecular geometry (2 domains) |
AX2 linear |
molecular geometry (3) |
AX3 trigonal planar AX2E bent |
molecular geometry (4) |
AX4 tetrahedral AX3E trigonal pyramidal AX2E2 bent |
molecular geometry (5) |
AX5 trigonal bipyramidal AX4E see-saw AX3E2 T-shaped AX2E3 linear |
molecular geometry (6) |
AX6 octahedral AX5E square pyramidal AX4E2 square planar AX3E3 T-shaped AX2E4 linear |
sigma bond |
single bond head to head overlap |
pi bond ; |
in multiple bonds parallel overlap |
relative strengths of intermolecular forces |
ion dipole hydrogen bonding dipole dipole dispersion forces |
empirical formula |
simplest whole number ratio of elements |
molecular formula |
exact number of atoms present |
combination reactions |
2 or more reactants combine to form one product |
decomposition reactions |
a compound breaks into two or more substances |
single displacement reactions |
an atom replaces an atom in another compound |
double displacement reactions |
atoms from two different compounds switch to form two new compounds |
limiting reactant |
reactant consumed first (least number of moles) |
percent yield |
actual/theoretical x 100% |
rate law |
aA + bB -; cC + dD ; rate = k [A]x[B]y ; |
Difference between rate constant and equillibrium constant |
stoichiometric coeffeicients don't equal orders of reaction
stoichiometric coeffecients do equal superscript in equilibrium |
steps in determining rate law |
1. look for 2 trials where all but one substance concentration is held constant 2. repeat for all reactants 3. plug concentrations in to determine rate constnat |
zero order reactions |
rate is independent of concentration k units: M/sec rate only changes with temperature |
first order reactions |
most common example is radioactive decay k units: 1/sec rate is proportional to concentration of one reactant |
Second order reaction |
k units: 1/Msec |
factors that affect reaction rate |
|
equilibrium constant |
aA + bB -> cC + dD
Kc = [C]c[D]d [A]a[B]b |
What does Keq tell us about products and reactants? |
Keq >> 1 products > reactants Keq << 1 reactants > products Keq ~ 1 reactants ~ products |
LeChatelier's Principle |
determines direction reaction will proceed when subjected to stress |
effects of concentration on reaction direction |
A + B ; C + D ; A increases, shifts to products D decreases, shifts to products |
effect of pressure and volume on reaction direction |
Increase in pressure shifts equilibrium to side with fewer moles ; Reduction in volume shifts equilibrium towards products |
What will shift equilibrium towards products? |
reactants added products taken away pressure applied volume reduced temperature reduced (if heat is a product) |
What will shift equilibrium towards reactants? |
product added reactants taken away pressure reduced volume increased temperature increased (if heat is a product) |
system |
part of universe being studied |
surroundings |
everything outside of the system |
isolated system |
can't exchange matter or energy |
closed system |
can exchange energy but not matter |
open system |
can exchange both matter and energy |
isothermal process |
temperature of system remains constant |
adiabatic process |
no heat exchange occurs |
isobaric process |
pressure of system remains constant |
enthalpy |
ΔHrxn = Hproducts - Hreactants
Bond formation is always exothermic (releases heat) Bond dissociation is always endothermic (requires energy) |
entropy |
ΔS = Sfinal - Sinitial
ΔS = qrev/T
ΔSuniverse = ΔSsystem + ΔSsurroundings
ΔSuniverse > 0 in spontaneous reactions |
Gibb's free energy |
;G = ;H - T;S ; ;G ; negative ; spontaneous ;G ; positive ; nonspontaneous ;G ; zero ; equilibrium |
Standard Gibb's free energy |
ΔGº = -RT ln Keq
ΔG = ΔGº + RT ln Q
|
STP |
standard temperature pressure T = 0ºC |
Standard state |
T = 25ºC used in standard enthalpy/entropy problems |
Boyle's law |
pressure and volume are inversely related P1V1 = P2V2 |
Charles' Law |
volume and temperature are directly proportional
V1/T1 = V2/T2 |
Ideal Gas Law |
PV = nRT
d = m/V = P(MW)/RT |
Partial pressures |
Ptot = PA + PB + PC
PA = PTXA XA = nA/nT |
When do real gases deviate from the ideal gas law? |
at high pressure, low temperature, and temperatures close to the boiling point
V will be less than predicted |
Assumptions of the Kinetic Molecular Theory |
|
diffusion of gases |
heavier gases diffuse more slowly than lighter ones
r1/r2 = √((MW2)/(MM1)) |
transition between liquid and gas |
evaporation: liquid to gas condensation: gas to liquid |
boiling point |
vapor pressure of liquid is the same as the external pressure
|
transition between solid and liquid |
melting (fusion): solid to liquid solidification (crystallization): liquid to solid |
solid to gas direct transitions |
sublimation: solid to gas deposition: gas to solid |
osmotic pressure |
∏ = MRT
water will move towards greater molarity or higher temperature |
Solubility: salts of alkali metals |
always soluble |
Solubility: salts of ammonium ion |
always soluble |
solubility: chlorides, bromides and iodides |
soluble unless Ca, Sr, Ba, Pb |
Solubility: metal oxides |
insoluble except CaO, SrO, BaO |
Solubility: hydroxides |
insoluble except alkali metals an Ca, Sr, Ba |
Solubility: carbonates, phosphates, sulfides, and sulfites |
insoluble except alkali metals and ammonium ion |
electrolytes |
solutes whose solutions are conductive |
percent composition by mass |
mass solute/mass solution x 100% |
mole fraction |
moles compund / total number moles |
molarity (M) |
mol solute/L solution |
molality (m) |
mol solute/kg solution |
normality (N) |
g solute/L solution |
solubility constant |
Ksp = [An+]m[Bm-]n |
solubility constant vs. reaction quotient |
Ksp > Q solute will continue to dissolve Q > Ksp precipitation will occur Q = Ksp equilibrium |
common ion effect |
if a salt is added to a solution already containing one of the ions, the equilibrium will shift to favor the solid salt |
conjugate acid-base pairs |
related by the transfer of a proton |
acid: __________ide |
hydro_____ic acid |
acid: _____ite |
_____ous acid |
acid: _____ate |
_____ic acid |
pH |
-log[H+] |
pOH |
-log[OH-] |
Kw |
=[H+][OH-]
= 10-14
pH + pOH = 14 |
dissociation of strong acids and bases |
completely dissociate into component ions |
Ka |
Ka = [H3O+][A-]/[HA]
measures degree to which acid dissociates |
stength of acid compared to Ka |
weaker acids have smaller Ka's |
amphoteric (amphiprotic) |
acts as both an acid and a base |
titration: strong acid + strong base |
quivalence point is at 7 |
titration: weak acid + strong base |
equivalence point is in the basic range |
buffer |
mixture of a weak acid or base with its salt |
Hendersen-Hasselbach equation |
pH = pka + log[A-]/[HA] |
polyprotic acid titrations |
have more than one equivalence point ; (each equivalence point corresponds to the loss/gain of one electron) |
oxidizing agent |
causes atom to undergo oxidation |
reducing agent |
causes atom to be reduced as the agent itself is oxidized |
LEO the lion says GER |
lose electrons = oxidized gain electrons = reduced |
oxidation number of free elements |
zero |
oxidation number of monatomic ions |
equal to the charge state |
oxidation state of group IA and IIA elements |
+1 and +2 respectively |
oxidation state of halides |
-1 unless attached to a more electronegative atom |
oxidation state of hydrogen |
+1 unless attached to a less electronegative atom |
oxidation state of oxygen |
usually -2 |
What is the sum of the oxidation numbers equal to? |
0 in a neutral compound |
Steps in balancing a redox reaction |
|
Galvanic vs. electrolytic cells (in terms of Gibb's free energy) |
Galvanic cells have spontaneous reactions so -ΔG
|
electrodes |
where reaction occurs |
anode |
where oxidation occurs (AN OX) |
cathode |
where reduction occurs (RED CAT) |
salt bridge |
allows for exchange of cations and anions |
conventional representation of a cell |
anode | anode solution || cathode solution | cathode |
anode charge in galvanic and electrolytic cells |
positive in electrolytic cells negative in galvanic cells |
reduction potential |
tendency of a species to aquire electrons and be reduced
a more positive Eº means greater tendency for reduction to occur |
electromotive force (EMF) |
difference in potential between two cells
positive in galvanic cells
negative in electrolytic cells |
Nernst equation |
nFE°cell = RTlnKeq |
what information does a positive E°cell give? |
K is postive so product formation is favored |