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36 Cards in this Set

  • Front
  • Back
Ionization Energy
energy required to remove an e-
electron affinity
energy required to add e-
-EA = energy emitted = stable octet
+EA = energy absorbed = break octet
Zeff (effective nuclear charge)
strength of p+ pull on e-
diamagnetic
all e- spin paired --> repulsion in magnetic field
paramagnetic
not all e- spin paired --> attraction in magnetic field
NBE (nuclear binding energy)
energy released when nucleons seperated
Shielding
valence e- in shell around nucleus, with more shells; greater shielding
Ionic Radius Trend
cation+ < neutral atom < anion-
Polar Covalent Bond
difference in EN results in unequal e- sharing, resulting in dipole moments
ie. HF : +----->
Coordinate Covalent Bonds
only one atom is donating both e-, acting as Lewis base or ligand
Intermolecular Forces
1. dipole dipole
2. ion dipole
3. dipole induced dipole
4. London dispersion forces
5. Hydrogen bonding
1. +ve attracted to -ve end of dipoles
2. cation/anion attracted to dipole
3. one dipole induces instantaneous dipole in another
4. instantaneous dipoles in NONPOLAR molecules
- > depends on polarizability of molecule (based on environment
5. H+ interaction with F, O, N attached to H
Solvation
solvent molecules around solute
Why use molality over molarity?
used when T is changing,
because m remains constant with change in P or T; while M does not
What forms do solutions come in? (in terms of combos of the three phases)
gas + gas
gas + liquid
liquid + liquid
liquid + solid
solid + solid!!!
Why does like dissolve like?
Are able to replace intermolecular forces with equal or stronger forces
Colligative Property
independant of identity of particle, and dependant on # of solute particles (van't Hoff factor) ; thus effective concentration (iM)
Vapor Pressure: What happens to vapor pressure when solute added? When is this assumption not reliable?
- Pvap is the gaseous form of the liquid, that exerts pressure on exposed liquid surface
- Pvap depression, as more E req'd to escape
- Not reliable when working with volatile substances (weak intermolecular forces)
Osmotic Pressure
pressure to STOP osmosis (movement of H2O from low to high [conc] across semi permeable membrane)
What is an intermediate and when is it formed?
short lived as the activated complex of the steady state approximation during the rate determining step where is shuttles back and forth between phases
Are transition states and intermediate the same thing?
No TS cannot be isolated (are theoretical constructs ) and are of the highest energy
Catalyst
lowers activation energy of the rate determining step; undergoing temporary changes but unchanged after the reaction, by stabilizing the TS
Rate Law
rate at which reactants and products disappear; only using reactants of the rate determining steps and is determined experimentally
What is the rough rule with changes in temperature and rate law?
10 degree increase results in rate increase by 2 to 4 times
What is the difference between the k constant of rate law and the equilibrium constant (Keq)?
for rate law, the k constant is dependant on the reaction, while Keq is CONSTANT for a given Temp.
In UCM, why doesn't an object fall to center, since the Fc=Fnet points towards the center?
it is falling towards the center, but speed keeps it in motion; and direction of velocity does NOT equate to direction of Fnet
Is torque a force? Why or Why not?
No, it is a vector but only a property of a force ; because does rotational movement (not push or pull) and measured in Nm, rather than N
When is torque not present?
when force is applied in parallel to motion
sin180 = 0 ; thus: torque = 0
Spontaneous Movement
PE <0 and G< 0
What is characteristic of perpendicular forces?
1. do NO work
2. can NOT change speed, only direction
Amphoteric vs. Polyprotic
Ampho - act as base or acid
Poly- more than one H+ with decreasing acidity strength
What conjugate base is always amphoteric?
the conjugate base of a weak polyprotic acid
State function
independant of path taken
ex. enthalpy
Bond Disociation Energy
energy req'd to break bond homolytically (form radicals)
Oxidation State vs. Formal Charge
ox state - to determine exchange of e- in redox
FC - to determine charge of most stable form of molecule
Oxidizing agent
is reduced (GER- gain e-)
In redox, how does dissolving compare to precipitating?
dissolving - lose e- (ox)
precipitating - gain e- (red)