Gly, Ala, Val, Leu, Iso, Phe, Tryp, Met, Pro: ND RD
Gly, Ala, Val, Leu, Iso, Phe, Tryp, Met, Pro: ND RD
Cd
2
Sn
2
Hg
(2)2
Hg
2
Au
1,3
Pt
2
Pb
2
Bi
3
cations are smaller than anions bc oI radius.
Coulomb`s law: Fkq1q2/r
2
describes electrostatic Iorces holding e to
nucleus.
in atoms with more than 1 e-tron, there is e-
shielding. 2
nd
e-tron doesn`t Ieel entire charge.
2
nd
e`tron`s Ieel oI charge called
effective nuclear charge (Zeff) -
ZeII Z minus avg # etrons b/w nucleus and
e`tron in question.
Periodic Trends
Zeff increases leIt to right. each electron is
pulled in more strongly toward nucleus
smaller atomic radius.
Atomic radius increases Irom top to bottom.
ionization energy E required to remove
electron. increases Irom leIt to right, and Irom
bottom to top. explained by ZeII.
Electronegativity tendency oI atom to
attract electron in bond that it shares w/
another atom. Pauling scale goes Irom 0.79 at
bottom-leIt oI chart to top-right, Florine.
undeIined Ior noble gases.
Electron affinity willingness oI atom to
accept additional electrons. increasees leIt to
right and bottom to top. most exothermic top
right.
metallic character increases Irom right to leIt,
top to bottom.
easy way to remember 5 periodic trends:
iI begins with an E, then it increases going to
the right and up. II it doesn`t begin with E,
then it increases oppositely so. ionization
energy is known as energy oI ionization. ZeII
is not considered Ior this mnemonic. Also,
these are just trends, and are violated
Irequently. Try to group Hydrogen as above
Carbon.
top-right trend E of ioni:ation, e-affinitv,
electronegativitv.
bottom-left trend Atomic radius, metallic
character.
SI Units, PreIixes Important Ior all MCAT
Sections
7 base units in SI system:
Mass kg
Length m
Time s
E current- A (ampere)
Temp K
Luminocity cd (candela)
Amnt oI substance mol
Force 1 newton: 1N 1kg m / s
2
common prefixes:
Mega (M) 10
6
Kilo (k) 10
3
Deci 10
-1
Centi- 10
-2
Milli (m)- 10
-3
Micro (u) - 10
-6
Nano (n) - 10
-9
Pico (p) - 10
-12
Bonds
covalent (shared electrons)
negative e`s pulled toward both positvely
charge nuclei by electrostatic Iorces. 'tug oI
war repulsive and attractive Iorces balance
out until bond length is met (equilibrium,
lowest energy).
E required to break bonds, no energy is
released. compound is 2 or more elements.
ratio is empirical Iormula.
bond energy E required to break bond.
mass of element in molecule weight oI
element / weight oI molecule
empirical formula from mass take 100g
sample. put weight oI element over its molar
mass # oI moles. do the same Ior the other
element. Compare their relative ratios
empirical Iormula.
Nomenclature
Ionic cpds named aIter cation and anion.
roman numeral I or II reIers to 1 or 2.
also, cupric higher charge, cuprous lower
charge. cation name in Iront oI anion name.
Monatomic/simple anions 'ide
polyatomic anions w/ multiple oxygens: ite
(Iewer) or ate (more), depending on # oI
oxygens. hypo and per are least and most
oxygens, respectively.
Acids: named by their anions.
molecular cpds w/ only 2 elements: name
begins w/ element towards bottom leIt.
Chemical Rxns, Eqns
physical rxns are melting, evaporation,
dissolution, rotation oI light. molecular
structure maintained.
chemical rxn molecular structure changed.
eg, combustion, redox. common combustion:
CH4 2O2 CO2 2H20
*MCAT will give balanced eqn unless
otherwise stated
runs to completion - runs to right until supply
oI at least 1 oI reactants is depleted. rxns oIten
don`t get here bc get to equilibrium Iirst.
limiting reagent that which would be
completely used up iI rxn were run to
completion
Chemical Yield Actual / Theoretical
x100 Percent Yield.
Fundamental Rxn Types
Combination: A B C
Decomposition: C A B
Single Displacement/Replacement:
A BC B AC
Double Dis/Replacement / Metathesis:
AB CD AD CB
Rxn Symbols
A means change in. or heat is added iI above a
rxn arrow.
double arrow means equilibrium can be
reached
means there are resonance structures.
] indicates concentration
indicates standard state conditions
Bonding in Solids
solids can be crystalline or amorphous.
ionic crystals oppositely charged ions held
together by electrostatic Iorces.
Molecular crystals composed oI individual
molecules held together by intermolecular
bonds. eg, ice.
Quantum Mechanics
elementary particles can only gain or lose
energy in discrete units. eg, walking up stairs.
-Quantum numbers
a set oI 4 numbers as ID Ior an e- in given
atom. no 2 e`s have same 4.
1
st
is principal quantum number: n.
designates shell level. the larger, the greater
size / E oI orbital. outermost shell designated
by rows.
Valence e`s contribute most to element`s
chemical properties. located in outermost
shell. typically only s and p shells.
2
nd
is azimuthal quantum number: !.
designates subshell. these are orbital shapes: s
(l 0), p (l1), d (l2), and I (l3).
! n-1
s subshells look like sphers
p subshells look like peanuts
3
rd
: magnetic quantum number: ml-
designates precise orbital oI subshell. each
subshell has possible ml values Irom ! to !.
so Ior Iirst shell n1, ! #0, only possible ml is
0.
For n 3, 5 possible orbitals with ml equaling
-2, -1, 0, 1, 2.
4
th
number is e- spin number: ms. can be
or . Pauli exclusion principle no 2 e`s
can have same 4 coordinates.
Heisenberg Uncertainty Principle
dual nature of matter wave and particle
inherent uncertainty in product oI a particle`s
position and its momentum. on the order oI
Planck`s constant (6.63e-34 J-s).
Energy Level oI Electrons
Aufbau principle each new proton added
Ior new element, new e-tron added, as well.
Nature preIers lower E state. more stability.
electrons thus look Ior orbital with lowest e
state whenever they add to atom. lowest
subshell.
Electron conIiguration lowest to highest
energy subshells
1s
2s2p
3s3p3d
4s4p4d4I
5s5p5d5I
iI we Iollow arrows, they show us order oI
increasing energy Ior subshells. not
necessarily in numerical order: eg, 4s subshell
lower energy level than 3d.
1s2s, 2p 3s, 3p 4s 3d 4p
5s.
Think oI 'd as dilatory in the order.
*total number oI e`s in your conIiguration
should equal that Ior atom / ion.
Like charges repel. iI placed close to each
other, PE. explains why only 2 electrons can
Iit into one orbital.
explains Hund`s rule: e`s will not Iill any
orbital in same subshell until all orbitals in
subshell contain least 1 electron. unpaired
electrons will have parallel spins. (bus to
camden)
This is moderated by having to climb an extra
energy step.
2p
2s
1s
BeIore 2p will start Iilling, 1s and 2s must be
paired.
Planck`s quantum theory: electromagnetic E
is quantized in discrete units.
AE hf
(where h Planck`s constant 6.6e-34 J-s).
Einstein: iI we think oI light as particle (ie,
photons), we can use same equation.
deBroglie: wave nature oI electrons Iollow
equation
h / mv
when electron Ialls Irom higher E rung to
lower E rung, energy given oII in Iorm oI
photon.
photon must have Irequency which
corresponds to energy change AE hf
The reverse is true: photon collides w/
electron, it can only bump electron to another
rung.
photoelectric effect- one-to-one photon to
electron collision. proved light is made oI
particles (einstein). KE ectrons increases only
when intensity is increased by Irequency oI
photons. minimum E required to eject an
electron called work Iunction, 4, oI metal.
KE oI ejected electron given by E oI photon
minus work Iunction
KE hf - d
--------------------------------------------------------
Gases Kinetics and Chemical Equilibrium
gas loose collection oI weakly attracted
atoms moving randomly.
STP - 0C and 1atm
speed 481 m/s at STP
mean free path distance traveled by gas
between collisions ~ 1600Angstroms
unlike liquids, all gases are miscible w/ each
other, regardless oI polarity. with time and
low temp, heavier gases settle below lighter
ones
Ideal gas obeys ideal gas law:
PV nRT
where P is in atm, V in litres, T in Kelvin, and
R is universal gas constant (0.082 L-atm /
mol K)
ideal gas:
1) zero volume; 2) no Iorces other than
repellant 3) completely elastic 4) avg KE u T
STP 1 mole oI any gas occupies 22.4 L
partial pressure total pressure oI mixture
times mole Iraction oI gas
Pa XaPtotal
where Xa moles a / total moles oI gas
Dalton`s Law total gas pressure is sum oI
partial pressures oI each gas.
Ptotal P1 + P2 + P3..
KEavg 3/2 RT
valid Ior both gases and liquids
in sample oI gas, KE oI molecules will vary
Irom molecule to molecule, but there will be
average oI the KE oI the molecules that is
proportional to the T and independent oI the
type oI gas.
Graham`s law; v1/v2 \m2 / \m1
Effusion: spreading oI gas Irom high P to low
P through a 'pinhole.
eIIusion rate1 / eIIusion rate2 \m2 / \m1
Diffusion spreading oI one gas into another
gas or into empty space. approximated by
Graham`s law.
Real Gases
deviate Irom ideal behavior when molecules
are close together. volume oI molecules
become signiIicant compared to volume
around molecules. High pressure / tiny
container, low temp.
Basically, real gases take into account their
own volume, so
Vreal > Videal.
2
nd
, real gases exhibit Iorces on each other. so
P real < P ideal
Chemical Kinetics
study oI rxn mechanisms, rates.
typically deals w/ reaction as it moves towards
equilibrium (eg, how Iast it`s achieved).
collision model reactants must collide.
activation E threshold
Arrhenius eqn: k zpe
-Ea/RT
where z collision Irequency.
rate oI rxn increases with T.
Equations Ior Rxn Rates
rates given in molarity per second (mol/L-s)
aA bB cC dD
rate -1 AA] -1 AB] 1 AC] 1 AD]
a t b c d
Intermediates products oI one step,
reactants in another. OIten at very low
concentration.
rate law Ior Iwd rxn
rateforward kfA]
o
B]
where alpha and beta are the order oI each
respective reactant, the sum oI them are the
overall order.
Determining the Rate Law by Experiment
relatively simple.
consider
2A + B + C 2D
compare a pair oI trials at a time
iI concentration doubles and rate doubles, then
superscript is 1. iI rate quadruples with
doubled concentration, exponent oI 2. iI rate
does not change with doubling oI a
concentration, that exponent is zero.
add the exponents eg, third order.
Reversible Rxns
slow step rate determining step. steps prior
to it can still contribute to rate law.
use equilibrium concentration oI any
intermediates.
Catalysis
catalyst substance that increases rate oI rxn
w/o being consumed or permanently altered
lower the Ea. creates new rxn pathway which
includes an intermediate
-heterogeneous in diII phase than reactants
and products
-homogeneous same phase
Iirst order uncatalyzed rxn example:
rate k0|A|
new one would be (iI cat by acid):
rate k0|A| KH|H||A|
catalyst changes Ea, but not delta G.
EIIects oI Solvent on Rate
liquids have 100x more collisions than gas.
most with solvent no rxn.
solvation aIIects k. they can electrically
insulate reactants, reducing Iorces b/w them.
Equilibrium
chemical equilibrium Iwd rxn rate equals
reverse. no change in |pdts| or |rcts|
consider AB
Iorward rate law is rate kI|A|
reverse is rate kr|B|.
they are directly proportional to each other.
equilibrium |B| ~ |A|, kI ~ kr
rate deIinition
rate -1 AA]
a t
rate at equilibrium is zero. does not mean rxn
rate is zero.
K C]
c
D]
d
Products
coefficients
A]
a
B]
b
Reactants
coefficients
equilibrium constant depends only on T
don`t conIuse with equilibrium itselI.
K has no units. proportion activity.
good Ior all equations, including non-
elementary
*Do not include solids or pure liquids (eg
water)
Partial Pressure Equilibrium Constant
rxns Ior more than 1 pathway. any 2 or more
single rxns or series resulting in same products
Irom same reactants must have same Keq.
Kp is partial pressure Keq, n sum oI
coeIIicients oI products minus sum oI coeII oI
reactants.
Reaction Quotient
For reactions not at equilibrium.
Q Products
coefficients
Reactants
coefficients
use to predict direction oI rxn.
we always move toward equilibrium. QK
iI Q K equilibrium; iI Q~K,
products~reactants than when at equilibrium;
rxn rate reverse ~ Iwd left shift
iI Q K products reactants than when at
equilibrium . rxn rate Iwd ~ reverse. right
shift.
Le Chatelier`s Principle
when a system at equilibrium is stressed,
system will shiIt to reduce stress.
3 stressors
1) addition or removal oI pdt or rct
2) changing P oI system
3) heating or cooling system
consider the Iollowing:
N2(g) 3H2(g) 2NH3(g) Heat
iI we add N2 gas to rigid container, rxn moves
right. H2 partial pressure also reduced bc it`s
Iorward rxn. NH3 and heat created.
iI we raise T, rxn pushed to leIt. NH3
decreased.
iI size oI container reduced in constant temp,
or when solution is concentrated/diluted, rxn
moves to side oI least gas moles.
Does not alwavs predict correct shift.
exceptions include salts, solvation rxns, and
nonreactive gas. Helium does not affect
equilibrium at all.
Thermodynamics
study oI energy and macroscopic properties.
divide universe into system and surroundings.
System AE? AM?
Open Yes Yes
Closed Yes No
Isolated No No
State functions- physical condition oI system.
pathway independent.
extensive- change w/ amount in system. eg,
volume, number oI moles.
intensive- independent oI system`s size.
Pressure and temperature, eg.
Heat
aka, 'q. movement oI E via Always Irom hot
to cold (down the gradient).
1) conduction - mollecular collisions. requires
physical contact. substances conduct at
diIIerent conductivity, k.
2) convection heat txIer via Iluid
movements, such as air currents.
3) radiation. via e-magnetic waves. all
objects at T ~ 0K radiate some heat, some e-
magnetic waves. only type that txIers through
vacuum.
Work
any energy transIer that isn`t heat.
PV work a system at rest with no
gravitational PE or KE, but pressure and
volume change create work.
w PAV (constant pressure)
0
th
Law temperature exists
3
rd
law perIect crystal at 0 K is assigned
entropy value oI zero. all other substances and
all T`s have positive entropy value.
First Law of Thermodynamics
E oI system and surroundings always
conserved.
AE q + w
(where work on system considered positive)
Heat Engines
gas pushes against piston, now held by outside
Iorce we can control. heat gas, it expands
while at constant T. Total E oI gas does not
change as it expands. energy oI heat we`ve
added changes completely into PV work done
by Iorce against piston. heat oI liquid gets
disipated into a cold reservoir nearby.
compressed to original state, back to where we
started.
2
nd
law of Thermodynamics Heat cannot be
changed completely into work in a cyclical
process.
reverse oI heat engine reIridgerator.
Thermodynamic State Functions: Internal
Energy (U); Temperature (T); Pressure (P);
Volume (V); Enthalpy (H); Entropy (S); Gibbs
Energy (G).
Internal Energy
molecular energy such as vibrational,
rotational, translational, etc.
AU q + w
Temperature
how Iast molecules are moving / vibrating.
hot T bc oI more molecular movement.
Described by zeroth law.
avg KE oI single molecule in a Iluid:
KEavg 3/2 kT
Kelvin Celsius 273
virtually all phys properties change w/ T
Pressure
P oI ideal gas is random translational KE per
volume.
PV nRT
Enthalpy
extra capacity to do PV work. cannot be
intuited, just memorize equation:
AH AU + PAV
Standard State (not same as STP).
reIerence Iorm Ior a substance at any chosen
temperature T and P oI 750 torr.
Standard Enthalpy oI Formation AHf A in
E enthalpy Ior rxn that creates 1 mole oI cpd
Irom raw elements. the naught symbol
indicates standard state conditions. consider
water:
H2(g) IiO2(g) H20(l)
AHI -285.8kj/mol
For rxns involving no change in P, AHI q
Hess`s Law: When you add rxns, you add
their enthalpies.
AHf reaction AHf products - AHf rcts
endothermic positive enthalpy
exothermic negative enthalpy
top oI the hill in a rxn graph transition state
catalyst lowers Ea oI Iwd and rev. rxns
aIIects the rate, NOT the equilibrium, and
NOT the enthalpy.
Entropy
nature`s tendency towards disorder (S)
more likely u more entropy
2
nd
law of thermodynamics entropy oI an
isolated system never decreases.
AS(sys) + AS (surr) AS (univ) > 0
Iwd entropy (-) reverse entropy
'reversible Ea lower than Iwd Ea.
irreversible ' Opposite
Entropy, not energy, dictates direction oI rxn.
it increases
3
rd
Law of Thermodynamics zero entropy
Ior any pure substance absolute zero and in
internal equilibrium.
entropy units are J/K.
Gibbs Free Energy
equilibrium achieved by maximizing entropy
oI universe.
AG AH - TAS
a negative AG usually implies spontanaeity
it is a state Iunction. non-PV work. eg,
contracting muscles, transmitting nerves,
batteries.
deals with change oI enthalpy / entropy oI a
system.
II enthalpy, -entropy nonspontaneous
II enthalpy, entropy spontaneous
higher T Iavors direction Iavored by entropy
Solutions
solution: homogenous mixture oI 2 cpds in
single phase, eg, solid, liquid, gas.
solvent: compound which there is more oI.
solute: cpd oI which there is less.
Colloids
like soln, but only solute particles are larger.
eg, hemoglobin. usually can`t pass
semipermeable membrane.
More Solutions
dissolved when solute is mixed w/ solvent
like dissolves like nonpolar solvents
dissolve nonpolar solutes, etc.
London dispersion forces hold together
nonpolar molecules. weak interactions.
Ionic cpds dissolved by polar solvents.
break into cations and anions surrounded by
respectively charged ends oI polar solvent.
called solvation. Water does this really well.
H sides oI H20 would surround Cl- ion,
whereas O- side would surround Na ion.
water-solvated hydration. said to be in
aqueous phase.
water is poor conductor oI electricity unless it
contains electrolytes, cpds that Iorm ions in aq
soln.
Be aware oI some common ions:
nitrite NO2
-
, Nitrate NO3
-
, sulfite SO3
2-
,
sulfate SO4
2-
, hypochlorite ClO
-
, cholrate
ClO3
-
, perchlorate ClO4
-
, carbonate CO3
2-
,
bicarbonate HCO3
-
, phsphate PO4
3-
Units oI Concentration
Molarity (M) moles solute / volume
solution
Molality (m) moles solute / kg solvent
Mole fraction (X) mols solute / all mols
mass mass solute / total mass soln x 100
ppm mass solute / total mass soln x 10
6
'parts per million
Soln concentrations always given in terms oI
the Iorm oI the solute beIore dissolution
eg, 1 mol NaCL 1 L H20 approximately 1
molar solution NOT 2 molar, even though
NaCl goes to 2 ions.
Normality measures number oI protons per
acid. H2SO4 would be 2 normal, whereas HCl
would be 1 normal.
Solution Formation
Physical rxn:
3 steps: 1) breaking oI solute molecules, 2)
breaking oI solvent molecules, 3) Iorming
intermolecular bonds b/w solvent and solute.
E required to break bond.
heat oI soln given by
AHsol AH1 + AH2 + AH3
Iirst 2 steps endothermic, last is exothermic
breaking a bond always requires energy
input. solution with -AH will give off heat
when it forms. Solution that gives off heat
when forming creates stronger bonds w/in
solution.
positive heat oI solution weaker
intermolecular bonds than beIore
forming of solutions o entropy
(solutions usually more disordered than its
separated pure substances)
Vapor Pressure
Equilibrium b/w liquid and gas phases oI cpd
when it moves quickly. VP necessary to
bring liquid and gas phases to equilibrium is
vapor pressure oI the cpd.
Clausius-Clapeyron as it relates to VP:
ln(Pv) -AHvap (1) + C
R (T)
vaporization is ENDOthermic
so VP u T
when VP local atmosph pressure boil
melting is T at which vpliquid vpsolid
nonvolatile solute solute w/ no vapor
pressure.
Raoult`s Law (nonvolatile) iI 97 oI the
soln is solvent, then the vapor pressure will be
97 oI the vapor pressure oI the pure solvent.
Pv XaPa
Raoult`s Law (volatile) iI 97 oI soln is
solven, vapor pressure will be 97 oI the
vapor pressure oI the pure solven PLUS 3 oI
the vp oI the pure solute.
Pv XaPa + XbPb
Negative heats oI soln Iorm stronger bonds
and lower vp; Positive heats oI soln Iorm
weaker bonds and raise vp.
Solubility
solute`s tendency to dissolve in solvent.
on MCAT: usually salt in water.
reverse rxn: precipitation.
when rate oI dissolution precipitation
saturated.
Equilibrium of solvation rxn:
own eq constant, solubility product Ksp.
set equal to products over reactants raised to
their coeIIicients in balanced equation. leave
out pure solids, liquids.
eg, Ba(OH)2(s) Ba
2
(aq) 2OH
-
(aq)
Ksp Ba
2+
]OH
-
]
2
~solubility product changes only with tempereature
constant Iound in a book.
Solubility is the max number oI moles oI
solute that can dissolve in soln.
depends on T and ions
spectator ion ion w/ no eIIect on eq
common ion iI added to a saturated soln,
will shiIt Keq increasing precipitate.
unsaturated not in equilibrium
Solubility Guidelines
cpds with H20 solubilities oI less than .01
mol/L insoluble
Solubility Factors
solubility aIIected by P and T.
P on gas u solubility
Vpa u Xa
Henry`s law demonstrates that solubility oI
gas is proportional to VP. think oI opening a
can oI soda gas is released bc oI solubility
u pressure (u Temp)
T u Salt solubility
Heat Capacity, Phase Change, and Colligative
Properties
homogeneous system constant properties
various phases aqueous, pure liquid, vapor,
crystalline solid, amorphous solid.
Heat Capacity
measure oI E change needed to alter T oI
substance.
deIined as: C q given in cal /g - C
AT H20 1cal/g-C
q mcAT
either at constant V or P
Calorimeter
coffee cup calorimeter constant P.
measures E change at atmospheric P. can
measure heat oI rxn
bomb calorimeter - measures E change at
constant volume. measure heat oI water.
Phase Changes
graph with various slopes.
plateaus Ior heat oI Iusion, and later, heat oI
vaporization.
the slopes - mcAT
phase changes: melting/Ireezing;
vaporization/condensation;
sublimation/deposition.
each phase oI water has its own speciIic heat
(diIIerent slopes oI the lines)
Evaporation partial p above liquid vp
liquid. atmospheric P ~ vp.
Entropy positive Ior melting and
vaporizing, positive Ior Ireezing and
condensing.
Phase Change Diagram
indicates phases oI substance at diIIerent P and
T. Temp on x axis, Pressure (atm) on y axis.
graph Iorms a Y shape with
left: solid; top/middle: liquid; right: gas
1atm line runs just above the triple point
changing Irom H20 to CO2, we see the \ in the
letter Y move towards middle; 1atm line is
now intersecting solid and gas, only.
line separating solid and liquid has negative
slope in H20, but positive slope in CO2. Most
phase diagrams resemble CO2 in this respect.
negative slope in water explains why ice
Iloats; water is denser than ice. why? its
crystal structure takes up more volume
because oI the lattices.
Colligative Properties
properties that depend on 'how many and not
'what type.
vapor pressure, boiling point, Ireezing
point, osmotic pressure.
boiling point elevation eqn:
AT constant x m x i
m molality
i van`t Hoff factor, # oI particles a single
solut will dissociate into.
on MCAT, use the expected value oI van`t
hoII unless they tell you an 'observed one
that is less bc oI ion pairing.
addition oI nonvolatile solute bp elevation
addition oI nonvolatile solute mp
depression
same equation, diIIerent constant
osmotic pressure - tendency oI a solvent to
move into a solution. relative term when
comparing solutions
divid pure liquid by membrane that is
permeable to liquid but not solute.
H iMRT
where M is molarity iI the soln
osmotic potential partial measure oI system`s
Iree energy.
think oI osmotic pressure as pressure pulling
into a solution and hydrostatic pressure as
pusshing out oI a solution
H(b) pgh(b) - pgh(a) physics
Acids and Bases
3 deIinitions you must know:
Arrhenius anything that produces H ions
(acid) or OH- ions (base) in solution.
Bronsted-Lowry anything that donates a
proton (acid), anything that accepts a proton
(base).
Lewis most general. anything that accepts a
pair oI electrons (acid), anything that donates a
pair oI electrons (base).
Any aqueous soln contains both H, OH-
think oI acid as H, base as OH-.
acidic soln: greater |H| than |OH-|
basic soln: the reverse
neutral soln: equal concentrations
pH -logH+]
log(AxB) log(A) log (B)
each one unit oI pH represents a 10-Iold
diIIerence in H concentration
HA + H2O A
-
+ H30
+
acid base conj. base conj. acid
the stronger the acid, the weaker the conj. base
the stronger the base, the weaker the conj. acid
Kw KaKb
Many rxns in living cells involve proton
transIer. the rate oI such rxns depend on the
pH.
amphoteric substances act as either base or
acid, depending on environment. eg, water.
can act as base (accepting proton), or acid
(donating proton).
Strong Acids: HI, HBr, HCl, HNO3, HClO4,
HClO3, H2SO4
Strong Bases: NaOH, KOH, NH2
-
, H-,
Ca(OH)2, Na2O, CaO.
polyprotics on the MCAT pay attention to
Iirst one, unless Ka values diIIer by less than
10
3
'strong acid or 'strong base completely
dissociates in water.
3 Iactors contributing to acid strength
1) strength oI H- bond. 2) polarity oI bond.
3) stability oI conj base.
oxyacids: more oxygens u acid strength
Hydrides cpd with 2 elements, one oI which
is hydrogen. basic ones are group 5, acids are
group 6.
autoionization of water:
H2O H2O H3O
OH
-
Kw |H||OH-|
(h30 is equivalent to saying 'h plus)
Kw 10
-14
so iI solution is pH 2, ion concentrations will
be |H| 10
-2
mol/L ; |OH-| 10
-12
mol/L
larger the Ka and the smaller the pKa, the
stronger the acid. eg, Ka ~ 1; pKa 0.
same is true Ior Kb and pKb oI a base
acid dissociation constant Ka:
Ka |H||A-|
|HA|
equilibrium constant for that acid`s conj.
base w/ water:
Kb |OH-||HA|
|A-|
(iI you multiply Ka x Kb equations, you`ll
come out with Kw).
pKa + pKb 14
Finding pH with strong acid:
eg, 0.01 M HCl will have 0.01 mol/L oI H ions
0.01 10
-2
; -log ans 2. pH 2
Finding pH of strong base:
0.01 M NaOH soln. 0.01 mol/L oI OH- ions
pOH will equal 2, so pH equals 12.
double check that your pH makes sense. iI
base, pH always ~7.
Finding pH with weak acids:
given 0.01 M HCN
1) set up Ka equation:
Ka |H||CN| 6.2x10
-10
|HCN|
2) assume x mol oI HCN has dissociated. so x
mol oI H plus x mol oI CN. plug it into your
equation above:
Ka |x||x| 6.2x10
-10
|0.01|
3) solve Ior x. double check your pH is
reasonable.
4) Ior a base, the process is the same, except
what pops out is pOH. make sure you subtract
Irom 14 to get pH.
Salts
ionic cpds that dissociate in water.
Na and Cl- are conjugates oI NaOH and HCl
so it produces a neutral solution.
Remember that all cations, except metals (such
as Ca2, Sr2, Ba2), act as weak lewis acids
in aq solns.
Titrations
drop-by-drop mixing oI an acid and base.
perIormed to Iind the concentration oI some
unknown by comparing it with known
concentration oI titrant.
titration curve oI strong acid titrated with
strong base (base added to acid) is sigmoidal,
with mid point usually equaling pH oI 7. but
not with diprotic acids.
iI starting with base in a titration, sigmoid
starts at a high y intercept
iI starting with acid in titration, sigmoid starts
at low y intercept.
Titration oI weak acid w/ strong base
y intercept is slightly higher than rock bottom
there are 2 plateaus, not 1
half equivalence point: where pH pKa; at
middle oI 1
st
plateua, equivalence point is on
the second slope in the middle.
end point range is a little bit above and below
equivalence point.
buffer zone: the plateau where the
equivalence point lies. you can add the largest
amount oI base or acid with the least amount
oI pH change.
Henderson-Hasselbach equation:
pH pKa log |A-|
|HA|
basically says, ' halI equiv point, pH pKa
oI the acid.
halI equivalence where |acid| |base|
on MCAT realize that adding small amount oI
water to ideally dilute, buIIered solution will
have no eIIect on the pH.
To Find equiv point, we use an indicator.
usually weak acid whose conj. base is a diII
color. 'endpoint where indicator changes
color, i.e., changes into conj base.
Polyprotic Titrations
assume 1
st
proton completely dissocaiates.
two equiv points, two equiv points. pKa1
and pKa2
Electrochemistry
redox rxn: e`s txIerred Irom one atom to
another. OIL RIG.
eg, 2H2 O2 2H2O
when H is oxidized, oxi state has increased
Irom 0 to 1.
when O is reduced, oxi state reduced Irom 0 to
-2.
oxidation state: possible charge value Ior an
atom w/in a molecule. sum oI each atom`s oxi
states must add up to net charge on molecule.
Oxi States worth Memorizing
Elements:
elemental atoms 0
Flourine -1
Hydrogen 1
bonded to metal -1
Oxygen -2
Compounds:
Group 1 elements 1
Group 2 2
Group 5 -3
Group 6 -2
Group 7 -1
(Iirst table has priority over 2
nd
)
reducing agent / reductant: cpd whose
element gives e-trons to atom
oxidizing agent / oxidant: compound
containing the atom that is being reduced.
Potentials
electric potential E associated w/ any rxn.
when you reverse the rxn, it`s E`s sign
switches
positive E voltage spontaneous rxn
negative E voltage endergonic
Nickel, Iron, Zinc, and water do not
spontaneously oxidize, or give up their
electrons.
halI reaction potential is NOT multiplied when
rxn is multiplied, but halI reactions are
ADDITIVE.
Galvanic/Voltaic Cell
turns chemical energy into electrical energy.
salt bridge electrolyte conduction solution
TEIET Terminals, electrodes, ionic
conductor, electrodes, terminal. emf is the
voltage b/w T and T.
electrodes
anode negative sign. oxidation happens here.
cathode positive sign. reduction happens
here.
'RED CAT mneumonic
both usually a strip oI metal in solution.
one side may be called a 'halI cell.
cell potential E / electromotive force (emf):
potential diIIerence between terminals when
not connected. connection reduces voltage
due to internal resistance in the cell.
electrons Ilow alphabetically
Irom anode to cathode.
bc electrons are negatively charged, like repels
like.
cell potential Ior galvanic cell always
Free Energy and Chemical Energy
AG -nFEmax
determines a spontaneous rxn
F is Iaraday`s constant (~100,000 C / mol)
wqV
AG -RTln(Keq)
where K equals eq constant
Q is where rxn does not yet equal equilibrium
if K 1 then AG 0
if K > 1 then AG < 0
if K < 1 then AG > 0
that is to say, iI rxn has Keq that`s greater than
1, it will be spontaneous at STP.
Nernst equation:
E E - 0.06 log (Q)
n
Concentration Cell
a cell that is taking place in two jars. never at
standard conditions.
never standard conditions, so use nernst.
galvanic cells have cell potential
electrolytic cells have (-) cell potential
Red Cat, An Ox
Physics
Key to solving probs: well drawn diagram.
write a know/want table.
vectors and scalars
vector has magnitude and direction
scalar has magnitude only
to add vectors, place head oI Iirst vector to tail
oI second vector, draw arrow Irom tail oI Iirst
to head oI second.
multiplying
vectors can be multiplied/divided by scalars
eg, mass (scalar) times accel (vector)
Iorce (a vector)
any vector can be broken up into component
vectors, whose sum is the original.
lengths of components through pythagorean
and
OHsind
AHcosd
these values w/ be provided
common MCAT triangles: 3/4/5; and 5/12/13
speed distance/t ; velocity displacement/t
a Av / t
velocity and accel not always in same
direction
UniIormly Accelerated Motion
constant a.
x x0 + v0t +1/2 at
2
v vo + at
v
2
vo
2
+ 2ax
vavg (v + vo)
2
Displacement versus Time Graph
displacement versus time.
upward slope: velocity
downward: - velocity
plateau: 0 accel
curve: /- accel
slope velocity
Velocity versus Time Graph
slope acceleration
Projectile Motion
separate the projectile path into perpendicular
components.
peak height of profectile given bv.
vosind \(2gh) when v. is zero.
acceleration on the ball is constant (-9.8m/s)
in the absence oI air resistance, mass does not
aIIect projectile motion.
Air resisance
surIace area u air resistance
irregular, rough objects u ' '
higher velocity u ' '
Mass u 1/air resistance, bc less aIIected by it.
(think oI an anvil versus hollow rubber
ball)
Force
inertia tendency to remain in present state
Mass- quantitative measure oI inertia (kg)
Weight gravitational Iorce on an earth (N)
on earth this is 'mg
Center of Mass - single point at which all
mass is concentrated. any Iorce here in any
direction, same magnitude oI acceleration.
sometimes CoM is not 'in the object (a ring)
center of gravity single point where Iorce oI
gravity can be applied to entire mass.
For MCAT assume CoM CoG
Iorces on MCAT:
1) gravitational force (mg);
2) electromagnetic force (charged object or
magnet)
3) contact force perpendicular to surIace
(aka normal Iorce) and/or parallel to surIace
(Iriction) mgcos
F(T)
fk
mgsin
mgcos
mg
Newton`s 1
st
Law: law oI inertia.
Newton`s 2
nd
Law: F ma
Newton`s 3
rd
Law: every Iorce has opposite
Iorce
Newton`s Law oI Universal Gravitation:
FGm1m2
r
2
G 6.67 e-11 m
3
/kg-s
F oI A on B equals F oI B on A
why earth doesn`t move when we jump on it?
too massive
F tiny a
huuuuuuuge mass
inclined plane
without Iriction, only Iorces are Fn and gravity
mgsin4
4
Shortcut to inclined planes:
Normal Iorce mgcos4
one portion counters some gravity
the rest is accel.
gravitational mgsin4
Circular Motion / Centripetal Force
acv
2
/r v
Fcmv
2
r Fc
r
Friction
1) Normal Iorce always perpendicular to
contact surIace
2) Fr always parallel to contact surIace
static friction Iorce oppositng motion when
contiguous surIaces are not moving rel. to each
other.
Kinetic friction Iorce resisting motion once
the two surIaces start sliding.
Ior any two surIaces, there are 2 coeIIicients oI
Iriction: us and uk.
fs usFn
fk ukFn
with tension problems, a box being held by a
string, iI no movement, F(T) mg
Hooke`s Law
Iorce due to stretched or compressed object
F -kAx
Equilibrium, Torque, and Energy
equilibrium: no translational / angular
acceleration
static equilib: all velocities 0
dynamic equilib: nonzero but constant v
Fupward Fdownward
Frightward Fleftward
Only system not in equilib MCAT tests is one
that experiences translational acceleration.
to solve these probs:
1) write equations as though it were in
equlibrium
2) beIore solving, add 'ma to side w/ less
Iorce
LF ma
Torque
twisting Iorce. clockwise or counter
clockwise.
product oI Force and position vector 'r
x F x l (assuming perpendicular Iorce)
r point oI rotation.
Solving torque probs:
Fupward Fdownward
Frightward Fleftward
xclockwise xcounterclockwise
T
mg1 mg2
In this example, mg1 and mg2 are clockwise
and equal in sum to Iorce oI tension T.
Forces upwards Forces downwards
also, the torques are equal
so Tx mgd mgL
Energy
units oI joule (J). Ior macroscopic systems
units oI electron-volt (eV) Ior microscopic.
one joule 1 kg-m
2
/s
2
KE mv
2
Potential Energy (U)
Ug mgh
Elastic Potential Energy
Ue k Ax
2
Systems
Law oI Conservation oI energy: constant E
Ebefore Eafter
Work
Work transIer oI energy via Iorce, measured
in Joules.
W Fdcosd Ior all Iorces except Iriction
W AK + AU
assuming no dissipation in Iorm oI heat
Conservative / Nonconservative Forces
Law oI Cons. oI Mechanical E
,AK[ [AU[
Nonconservative Iorces those that change
mechanical E when they do work. KE
Irictional Iorce and the pushing and pulling oI
animals.
Ior this: W AK AU
Work and Friction
AK + AU fdcosd
iI internal energy change is avail use Iormula
W AK + AU + AEi
Power
rate oI energy transIer. unit is watt (W).
equivalent to J/s. don`t conIuse with W work.
P AE
t
iI you know Iorce and time:
P W
t
P Fvcosd
Momentum, Machines, Radioactive Decay
Momentum:
p mv
given in kg-m / s
momentum is always conserved.
momentum is a vector.
Collisions
Elastic mechanical E conserved. no E
dissipated to heat, sound, etc. eg, atomic
collisions.
Ui + Ki Uf + Kf
Inelastic colliding objects lose some mech E
to internal energy.
Completely inelastic when colliding objects
stick together upon collision.
can use conserv. oI momentum Ior inelastic:
pi pf
can be Iurther broken down into
p(x)i p(x)f
p(y)i p(y)f
might have to use cos/sin to break into vectors
momentum is conserved beIore and aIter
collision.
Reverse Collisions
opposite oI completely elastic: one object
spontaneously combusts into 2.
---
Impulse (J) is equal to change in momentum
1 Ap
1 FavgAt
Amv FavgAt
Machines
iI you see on MCAT, ideal machines reduce
Iorce but don`t change work.
ramp: inclined plane. pushing an object up
ramp, you are pushing mgsin4.
W mgh
WFd
work is held constant, so
F o 1/d
lever based on torque. like ramp, allows us
to increase the distance over which Iorce acts.
pulleys are actually modiIied levers. multiple
tension strings add up to counter act mg.
Radioactive Decay
Particle Symbol
alpha u
4
2
beta
-
or
0
-1e
positron
or
0
1e
gamma
HalI-LiIe Problems
4 variables: initial amnt oI substance, Iinal
amount oI substance, number oI halI lives, and
the halI liIe. MCAT will give you 3 oI these.
electron capture :
201/80Hg
0
-1e --~ 201/79 Au
Mass DeIect
E mc
2
where c 3x10
8
m/s
Fission and Fusion
Fusion combining oI 2 nuclei to Iorm
heavier nucleus.
Fission- splitting oI single nucleus to 2 lighter.
Fluids
fluid liquid or gas. conIorms to shape oI
container. battleship Iloats bc ocean conIorms
to surIace so that always normal Iorce.
density 'heaviness oI Iluid units kg/m
3
m/V
compression oI a gas makes it more dense.
assume not possible Ior solids, liquids.
SpeciIic Gravity-
SG substance / water
know H20 density on MCAT:
water 1000 kg/m
3
1g/cm
3
Iluid pressure result oI molecular collisions.
P F/A in units Pascal (Pa)
sucking water out a straw, how`s it work? atm
pressure above water in straw lower than atm
pressure above water in cup.
Fluids at rest only perpendicular Iorces on it.
P gy
iI an open container exposed to air:
P gy + Patmosphere
Patmosphere 101kPa
gauge pressure measure oI pressure
compared to local atmospheric P
absolute P pgauge patm
hydraulic lift works via Pascal`s principle.
F1d1 F2d2 or F1A1 F2A2
Fbuoyant mgwater fluidVg
fraction submerged floating object
fluid
an object Iloating displaces its weight in Iluid,
a submerged object displaces its volume in
Iluid.
Fb doesn`t change w/ depth.
V AAh
Fb pg AAh
Fb pgAh
A
AP pgAh
random translational motion contributes to
Iluid P at rest
uniform translational motion shared
equally by all the molecules at a location oI
Iluid.
Ideal fluid 1) no viscosity; 2)
incompressible; 3) steady/laminar Ilow; 4) not
rotating.
most likely to show up on MCAT
assume non-changing volume.
water through a pipe has volume nr
2
xd
continuity equation:
Q Av
where Q Ilow rate
I pQ pAv
where I equals mass Ilow rate.
Ilow rates are constant in an ideal Iluid.
Bernouli`s Equation (memorize):
P + pgh + 1/2 pv
2
K
where K is Iluid-speciIic constant.
where h is distance above some arbitrary point
sum oI the three terms is constant throughout
the Iluid.
v \(2gh)
velocity oI Iluid as it leaves a spicket.
Non-Ideal Fluid- drag and viscocity act to
impede Ilow. the narrower the pipe, the
greater the drag. (greater velocity, too).
slower than ideal Iluid, but similar principles.
AP QR
SurIace Tension
although denser than H20, a needle can Iloat
on water. due to intensity oI intermolecular
Iorces per unit length.
capillary action Iluid may be pulled up a
thin tube. intermolecular/cohesive Iorces and
adhesive Iorces (sticking to each other and
sticking to the tube.
Solids
Stress F/A in units N/m
2
Strain Adimension / original dimension
strain responds to stress.
Modulus of elasticity stress/strain
3 moduli to know Ior MCAT:
1) Young`s modulus (E) |tensile|
2) shear modulus (G) |shear|
3) bulk modulus (B)
|compression/expansion|
E (F/A)/(A/ho)
G (F/A)/(A/xo)
B AP/(AV/Vo)
Waves
wave txIer oI momentum and E Irom one
point to another. Ior MCAT, assume ideal.
wavelength measured crest-to-crest
frequency (f) number oI wavelengths / time
units oI herts (Hz) or cycles/s
aka s
-1
v f
period (T) - reciprocal oI Irequency;
T 1/f
amplitude (A) maximum displacement Irom
zero.
velocity is dictated by the wave`s medium.
elasticity; inertia.
Ior a gas, velocity increases with temperature.
sound waves move more quickly thru hot gas...
intensity (I) pw
2
A
2
v
I P
4nr
2
Intensity levels and dB. iI intensity by a
Iactor oI 10, the decibels increase by the
'addition oI 10 decibels.
eg, Irom 30 W/m
2
to 3000 W/m
2
adding 20
decibels.
10log (I / Io)
where Io is threshold intensity (lowest we can
hear)
AI AB
x10 10
x100 20
x1,000 30
x10,000 40
wave phase horizontal shiIt oI wave on a
graph. 'out oI phase vs 'in phase.
Two or more waves can occupy same space.
superposition interIerence
Constructive sum oI displacements larger
displacement
Destructive sum oI displacements smaller
displacement
Beats case oI superpositioning waves.
fbeat [f1-f2[
piano tuner. he listens until beat Irequency is
zero.
beat Irequency alternating increase and
decrease in noise intensity. hearing the pitch.
Irequency creating this is the average oI the
Irequencies Irom piano and tuning Iork.
high pitch u high Irequency u high note
when wavelength crosses to a diIIerent
medium, wavelength changes, Irequency
remains the same.
standing wave string is still at the nodes
while waves move up and down at antinodes.
harmonic series list oI all wavelengths Irom
longest to shortest.
longest first harmonic (1) or Iundamental
wavelength. Iewest number oI nodes (2).
second harmonic (2) requires extra node.
harmonic series totally closed or open:
L n n (n1,2,3.)
2
where L distance b/w 2 ends oI string
and n number oI the harmonic.
when one end is tied down harmonic series is:
L n n (n1,3,5.)
4
standing waves cause string to resonate
natural, resonant Irequency.
vf
Simple Harmonic Motion perIect sin wave.
sinusoidal Iunction in time.
a(t) -w
2
x(t)
acceleration u -displacement u \I
Hooke`s law: F -mw
2
x
elastic potential energy: PE kx
2
F -kAx
periodic motion Ior mass on a spring
T 2n\(m/k)
pendulum exchanges energy b/w PE and
KE.
T 2n\(L/g)
on MCAT may come in the Iorm oI:
orbit oI planet as viewed Irom side, tetherball
around pole, electrons oscillating back and
Iorth in AC current.
Hooke`s law acceleration oI any system in
SHM u displacement u \I
iI hanging on a string and swinging:
FT mgcosd + m(v
2
/r)
wackem wiggle
w \(k/m) w \(g/L)
box on a pendulum
string
so we see that period oI a swinging string is
independent oI the mass on the end oI it.
Doppler EIIect
waves are unaIIected by speed oI their source.
iI source moves relative to receiver, each wae
w/ travel diII distance, so Irequency oI
receiver/observer will seem diIIerent.
Af v and A v
fs c s c
c is not necessarily speed oI light, can be speed
oI sound, radio, etc.
understand this qualitatively. when relative
velocity brings the observer and source closer,
observed Irequency and observed
higher Irequency u higher pitch
blue shift wavelength appears shorter
(source and obs closer than b4)
red shiIt oppositte
when objects are moving in same velocity,
Irequency change is zero.
Electricity and Magnetism
because oI history oI science, current runs in
opposite direction oI the electrons.
Charge (q) given in units coulombs (C)
Universal Law of Conservation of Charge-
universe has no net charge.
charg eis quantized. smallest unit is one
electron unit (e 1.6x10
-19
C). photon or
electron.
opposite charges attract, like charges repel.
Coulomb`s law:
F kq1q2
r
2
where k is coulomb constant oI 9x10
9
and r is distance b/w centers oI charge.
mass/gravity very similar to charge
Iield can be represented by lines oI Iorce
points in direction oI the Iield. (positive to
negative Ior e-Iields). positive test charge.
Electric field electrostatic Iorce / unit charge
E. vector pointing in direction oI Iield. units
N/C or V/m.
E kq1
r
2
in units N/C
FEq
WUqEd
VEd volts in units J/C
voltage due to point charge
V (kq)/r
Movement oI Charge
conductors - metals, allow e`s to Ilow Ireely
resistors - bad conductors, hold e`s tightly in
place. eg, diamond, glass.
can charge a conductor by induction.
current - moving charge. in units amps (A)
or C/s
moves in the direction oI () charge
think oI electrical movement like Iluid.
Circuits
circuit cyclical pathway Ior current
all substances resist Ilow oI charge
measured quantitatively with resistivity ()
measure oI this is called Resistance (R) in
ohms (O)
R (L) / A
iI a wire is doubled in length or its cross
sectional area is halved, R by Iactor oI 2.
(analogous to Iluids)
resistance x current voltage:
ViR (Ohm`s law)
Kirchoff`s first rule: amount oI current
Ilowing in amount oI current Ilowing out.
node any intersection oI wires.
Kirchoff`s second rule: voltage around any
path in a circuit must sum to zero.
battery adds energy to circuit increases
voltage Irom one point to another. rated with
electromotive force (EMF), aka voltage.
assume no internal resistance on MCAT.
capacitor temporarily stores energy in a
circuit. parallel plate capacitor separated
by small distance. creates E Iield that is
constant everywhere b/w the plates. E Iield
given by
E 1 Q
K Ac0
Q charge on either plate: Eo is constant.
capacitance ability to store charge per unit
voltage.
C Q
V
the Iarther apart the plates, the greater the
voltage, the lower the capacitance.
C u A / d
Q CV
U QV CV
2
Q
2
/ C
dielectric constant, K - substance between
plates oI capacitor. must be insulator, to allow
buildup oI charge.
capacitor sign both plates same size
battery sign diII sizes
Reff R1 + R2 + .. (resistors in series)
1 1 + 1 + . (resistors
Reff R1 R2 in parallel)
1 1 + 1 + . (capacitors
Ceff C1 C2 in series)
Ceff C1 + C2 . (Capacitors in
parallel)
mneumonic: 'C, it`s inverted in the series
Power
power interchangable with mechanical
power
P iV i
2
R V
2
/R
2O 6V
2V
2V 2V
6V 2O
2O
0V
2O
0V
AC Current
direct current (DC) net movement oI etrons
in one direction around circuit.
alternating current (AC) oscillating e-trons
back and Iorth in SHM. in home outlets in
US. described as sine wave.
Vmax \2Vrms
imax \2irms
rms square root oI the average oI the squares
rms voltage in US is usually 120 Volts, 170
max.
Magnetism
measured in tesla, T. north and south poles.
a changing electric Iield creates a magnetic
Iield. a stationary charge does not create a
magnetic Iield.
B uo iLsind
4nr
2
Ior a long wire:
B uoi
2nr
right hand rule. thumb in direction oI current
(i) and grab wire, direction in which our
Iingers wrap is the direction oI magnetic Iield
(B).
F qvBsind
Iorce is directed perpendicularly to both
velocity and magnetic Iield.
2
nd
right hand rule: point thumb in direction oI
moving positive charge (v), point Iingers in
direction oI magnetic Iield (B) palm will point
diagonally in direction oI F.
qvB (mv
2
) / r
F ilBsind
A changing magnetic Iield electric Iield.
changing magnetic Ilux emI E
E - Ad
At
Faraday`s Law
Overall picture:
1) magnetic Iield is generated by moving
charge and;
2) moving charge experiences Iorce when
moving through electric Iield.
F qvB
Light and optics
electromagnetic wave traveling oscillation
oI electric and magnetic Iields. transverse
wave.
sppeed (c) at which wave propagates thru Iree
space is constant, equal to ratio oI magnitudes
oI electric Iield and magnetic Iield:
Light tiny sliver oI em spectrum. visible
light in wavelengths 390 to 700 nm
1nm 1x10
-9
m
shorter wavelength u violet light UV
longer wavelength u red light inIrared
each wavelength has corresponding Irequency
speed oI light in vacuum is constant.
Irom c I
c f
light slower when propagating thru medium.
index oI reIraction..
n c / v
when light crosses into new medium, I remains
same, but changes.
indeces on MCAT:
water- 1.3
glass- 1.5
plane-polarized light Iiltered light w/ all E
Iields oriented in same direction.
light`s dual nature propegates like a wave,
but has E transIormative properties like a
particle.
angle oI incidence measured Irom an
imaginary perpendicular line to the surIace. 4
oI incedence is between line normal and ray oI
light. 4 reIlection is between normal line and
deIlected light. 4 reIracted is the ray oI light
in new medium.
angle oI reIlection (same medium):
dincidence dreflection
angle oI reIraction (new medium):
n1sind1 n2sind2
Ephoton hf
higher Irequencies, such as violet and blue
light, have more E than lower I`s.
when light moves to higher n, 4 can be so
great as to cause total internal reIlection.
all photons reIlected angle oI reIlection, no
reIraction. 'critical angle.
Diffraction another type oI wave-bending
phenomenon. light thru small slit. size oI
opening ~ wavelength or smaller. constructive
vs destructive interIerence. smaller the
opening u larger the opening u greater bending
oI wave
Images
mirrors reIlect light; lenses reIract light.
our mind doesn`t account Ior light bending
in other mediums:
Person
water
real Iish brain`s Iish
An image may or may not exist:
virtual image does not exist outside oI mind
oI observer; no light rays emanate Irom virtual
image. no image would appear on paper. our
reIlection in a mirror. brain`s Iish above.
real image exists separately Irom obs. rays
oI light actually intersect and then emanate
Irom point oI intersection. iI sheet were there,
image would appear on it.
Mirrors and Lenses
mirrors convex and concave
lenses - converging, diverging.
concave looks like a cave, reverting back to
cavement would be a divergement.
always assume light originates Irom object.
thicker center converges
assume spherical mirrors Ior MCAT.
light Irom horizontal rays reIlected by concave
mirrors to Iocus on a single point, focal point.
Iocal point u radius oI curvature.
fmirror r
Iocal point is also aIIected by reIractive
indices oI lens and medium oI lens. also
aIIected oI radii oI curvature oI both sides.
power oI a lens. in units oI diopters (m
-1
):
Plens 1/f
Ray diagrams are not useIul Ior MCAT.
overview oI ray diagrams:
convex mirror (object same side): image
behind, upright, smaller, not real.
concave mirror: object same side, image
behind is upright, larger, not real.
Diverging lens: object Iar side, image Iarside
is upright, smaller, and virtual..
Converging lens: object Iar side, image
Iarside, larger, upright, and virtual.
lateral magniIication m ratio oI size oI image
to size oI object. h1 vs. h0
m -di hi
do ho
angular magniIication:
md di 4obj. to eye, Iront oI lens
dnp 4 obj. to eye, at near point
Ior any mirror or lens, distance oI imge related
to Iocal length and distance oI object:
1 1 + 1
f do di
hardest part is determining
when value is or -
In any double system, use Iirst image as the
object oI the 2
nd
.
Ior a convex mirror or diverging lens, I is
always negative.
Ior a concave mirror and converging lens, I is
always positive.
P 1 1 + 1
f di do
M -di hi
do ho
fmirrors r
Two lens systems
on MCAT would be microscope or teloscope:
M m1m2
Peff P1 + P2
Notes Irom 6.24.08
all nitrates & sodium salts are water soluble
single bond length ~ double ~ triple
given: Pb(OH)2 Pb2 and 2OH-
iI pH raised, rxn would shiIt leIt
P IV
'proton H ion
Photon E ejected electron E
ionization energy reached. all extra energy is
Ior the electron to have aIter ejection.
eg, iI 12 eV required to eject, and photon is
15eV, e- has 3eV oI KE.
KE electron u Voltage
Xray emmission u Intensity
W Fd
KE u evaporation
d at
2
Translational equilibrium all F`s cancel
acceleration is zero
u particle decay Helium ejection
dobject hobject
dimage himage
Cu(s) H2SO4 SO2 Cu
sulIur`s oxi state went Irom 6 4
Power work / time
Short period u short wavelength
Harmonic: 1
st
2
nd
3
rd
1 < 2 < 3
P1 < P2 < P3
f1 > f2 > f3
guitar harmonics always sound high
high pitch u high Irequency
P o wavelength o harmonic number o 1/f
harmonic multiple oI the original Irequency.
4
th
harmonic is 16x natural Irequency
as determined by 2
n
f v 3x10
8
m/s speed of light
voltage sources in parallel produce same
output voltage as single source; but iI in series,
their voltages would be additive.
Ireezing pt depression is colligative:
totally dependent on # oI solute particles in
water
molarity of solute o Tm
equiv point (first flat part) |Acid| and
|Conj. base| are equal.
'reducing agent causes reduction. eg, Fe.
----------------------------------------------------
BS
all somatic cells in body have same DNA /
Chromosomes regardless oI stage oI liIe
cholesterol precursor to steroid horomones
estrogen
vasoconstriction oI intestinal villi lacteals
Iat absorption
crossing Tt x Tt
one would expect Mendelian ratio oI 3::1 oI
tall to short plants
metabolism oI aa`s Irom proteins see
Nitrogen urine concentration u starvation
starvation: carbs, lipids used up, start breaking
down body proteins
CO bond makes molecule more polar
polarity u BP
chips, air bubbles break surIace tension oI
liquid, preventing superheating during a
vacuum Iiltration
Heat distillation Ilask slower rate better
Iractionation
Stereogenic carbon chirality center
diII makeup diII enantiomers
chiral iI 4 diII constituents
dbl bonded carbons are not able
to be chiral.
Boiling point: when vapor pressure oI liquid
surIace pressure
BP u surIace oI liquid
methyl ketone Iormation () iodoIorm test
acetone on the NMR 6H`s the same
singlet.
II rare gene, assume only 1 parent has it, and
that it`s recessive.
iI P phosphorylates R then
P splits /uses ATP ADP, and R becomes
phosphorylated: R-(p)
now activated.
to de-phosphorylate is to quickly deactivate
distal tubule reabsorbs glucose.
Hb Hg u GFR rate u reabsorption
albumin u hypertonic Hb
Ilow oI H20 Irom tissue to bloodstream
Protein such as pepsin operates well at pH oI 2
or 1.5, but iI as low as pH 1, will be denatured
and no longer operate.
PTH u Ca
2
Calciton(in) brings Ca
2
in-to bone
Parathy(rid) Ca
2
gotten rid Irom bone.
edema caused by albumin, body tissue
swelling.
KappacoIigus
KPCOFiGuS
------------- relatedness
(Br2 CCl4) turns colorless iI dbl bond
Iormed. 'dehydration
A B
removing pdt A as it is Iormed will cause a
leItward shiIt
Imprinting perception oI object enhanced
during critical development period.
Cyclohexane has lowest heat oI combustion
among cyclo-anes bc highly stable chair
conIiguration.
Steric hindrance bad nucleophile
Practice test notes
review circuits, plain mirrors, soln chemistry,
e structure, sound, atomic, nuclear structure,
skip VR nat sciences and double check them,
immune / circulatory systems, digestive
enzymes.
tend to have 10 min at end oI each section.
mark liberally.
PS
4 oI tilt most important in incline probs
van der walls, aka London dispersion
u polarizability
u boiling point
u number oI electrons
32g O2 1 mol O2
Doppler eIIect. As signal approaches,
Irequency gets higher.
Af -v
f c
where c is speed oI the medium
Csound Cradio
'apparent loss oI mass mass oI Iluid
displaced
'common ion eIIect saturated soln, eg NaCl
iI you add any other soln that has
Na or Cl-, you`re gonna get
precipitate
Resonant wavelength oI pipe or tube
open pipe has resonant wavelength 2xl
mechanical waves such as water/sound
only Energy is propegated
electrons have dual energy/matter
phenomenon
w/ Iixed potential diIIerence (voltage) between
cathode and anode, electric Iield u 1/L
E (V - IR) / L
electron cathode has V to voltage in eV
incedent photons only aIIect # oI electrons
emitted, not their energies.
electron accelerates Irom anode to cathode.
P I
2
R
(amps)x(ohms) Watts
electron ejections u current Ilow (I)
photon Irequency u speed oI ejected e-
radiation emitted when e`s orbital
currents in parallel resistors u 1/indiv resistors
BS
a-choline / morphine /heroin constricts
pupils. 'pinpoint pupils diagnostic oI opiate
intoxiIication.
nor/epinephrine Iight or Ilight / sympa
response dilated pupils
IR peak around 1700 CO double-bond.
Iungal spores metabolically inactive, haploid.
aldosterone Na reabsorption H20
reabsorption
impurities in any substance u melting (aka
Ireezing) point depression u decreased
intermolecular interactions. why? interrupts
intermolecular attraction.
intermolecular strength o boiling point
eg, why when you add salt to a pot oI water it
boils at a hotter temperature. because salt is
attracted to water.
amines soluble in dilute acid (eg, dilute HCl).
carboxylic acids soluble in dilute base.
ester hydrolysis ROH ROOH
DNA replicates in S phase.
saponification: ester (NaOH) Salt
(acid) ROOH
molecular weight oI cpds oI varying structures
should give a hint about the identity.
lung inIlation possible because oI negative
pressure by suction.
antibiotic resistance can be innate bc oI chance
mutations, eg, E Coli not killed with a Iirst
round oI antibiotics Ior inIection.
E Coli live in colon, move b/w colon and
appendix Ireely. outside oI them are
abdominal cavity.
Bacterial conjugation recombination.
Interneuron synapses pain, eIIerent neurons
to brain. Here are ealso the dorsal root
ganglion attached to sensory neuron, Ieeds
interneuron, interneuron tells the motor neuron
and eIIector to pull Iinger away Irom stove.
Bacteria versus viruses: bacteria can reproduce
via Iission.
\recessive people in populaetion # oI
recessive genes in all. the remainder are the #
oI dominant genes in all. Hardy-weinberg
says # of heterozygotes is equal to
2 x ( of dominant genes alleles)
x ( of recessive alleles)
aka 2pq.
Blood pressure:
depends on 2 things:
1) Cardiac output stroke volume x heart rate
2) resistance to blood Ilow
anti-inIlammatory drugs on a pt w/ septic
shock:
risk decrease oI endogenous antibacterial
deIense
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IIjI