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law of conservation of energy
energy cannot be created or destroyed
heat (q)
transfer of energy btwn two bodies at different temperatures (goes hot to cold)
endothermic
absorbs heat
qsys > 0
exothermic
releases heat
qsys < 0
heat capacity
C = q/∆T
specific heat capacity
C = q/m∆T
calorimetry
qsystem = -qsurroundings
internal energy (U)
total of all possible kind of energy in a substance
internal energy equation
∆U = q + w
work formula
-W = P∆V
enthalpy (∆H)
∆H = ∆U + P∆V
∆H = qp
what does enthalpy depend on
physical state!
enthalpy of exothermic reaction
∆H < 0
enthalpy of endothermic reaction
∆H > 0
Hess’s Law
if process can be written as a sum of several steps, enthalpy is the sum of the enthalpies during those steps
hess’s law equation
∆rH°=∑n(∆Hf°products) - ∑n(∆Hf°reactants)
waves
oscillation/periodic movement that can transport energy from one space to another
wavelength (λ)
distance btwn two peaks in a wave
frequency (v)
number of wave cycles that pass a specified point in space and time
speed of light equation
c = λv
nodes
points on the string btwn end points that are not moving
de brogile wavelength (where h is plak’s constant)
λ = h/mv
uncertainty principle
(∆x)(m∆v) >/= h/4π
atomic orbital
general region in atom where e- is most probable to reside
quantum #’s
n, l, ml, ms
quantum number: n
principal quantum number / shell number
general size and energy
= 1, 2, 3, …
quantum number: l
angular momentum number (shape of orbial and subshell)
= 0 ,1, 2, … n-1
l = 0
s
l=1
p
l=2
d
l=3
f
quantum number ml
magnetic quantum number
(spacial orientation, total number of possible orbitals)
= -l, -(l-1), 0, l-1, 1
quantum number: ms
direction of e- spin
= ½ or -1/2
hund’s rule
lowest energy configuration w/in set of degenerate orbitals is having max number of unpaired e-
pauli’s exclusion principle
no two e- in same atom can have exact same quantum numbers
ms must be different
aufbau principle
e- enter higher energy subshells only after low energy subshells have been filled to capacity
shape n=s (l=0)
one bubble
shape of n=p (l=1)
two bubbles
shape of n=d (l=2)
four bubbles
shape of n=f (l=3)
six bubbles
variation in covalent radius
when going down columns/groups, n increases
largest in bottom left corner
effective nuclear charge
Zeff = Z - shielding
Zeff
increases across periods
nuclear charge minus how well inner e- shield outer e-
ionization energy
energy needed to remove 2nd most loosely bound e-
ionization energy equation
X+ (g) —> X2+ (g) + e-
electron affinity (EA1)
energy associated with adding e- to a gaseous atom to from an anion
EA1 equation
X (g) + e- —> X-(g)
endothermic electron affinity
+EA
exothermic electron affinity
-EA