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energy
the capacity to supply heat or do work
potential energy
bonds
stored energy
speed of hot particles
fast
speed of cold particles
slow moving
thermal equilibrium
when one hot thing touches a cold thing, the kinetic energy transfers and thermal equilibrium will occur and they will start moving at the same pace
potential energy equation
mgh (mass x acceleration due to gravity)
kinetic energy equation
½ mv² (mass and velocity)
law of conservation of energy
energy cannot be created or destroyed, only transferred or transformed
aspects that affect heat transfer
size
starting temp of each substance
identity of materials
formula for heat energy
q = mcΔT
q = heat energy in joules
m = mass
c = identity
ΔT = change in temperature
heat capacity (C)
quantity of heat it absorbs or releases when it experiences a temperature chance of 1 degree celsius
extensive property
specific heat capacity (c)
the quantity of heat required to raise the temperature of 1 gram of a substance by 1 degree celsius
intensive
if a substance gains thermal energy (Tfinal-Tinitial), the value of q =
positive
if a substance loses thermal energy (Tinitial-Tfinal), the value of q =
negative
systems + surroundings =
universe
surroundings
the water the reaction takes place in
this is what we can monitor
system
the reaction itself
exothermic process
a change where system releases heat
endothermic process
a change where a system absorbs heat
skeletal equation of endothermic reactions
reactants + energy → products
skeletal equation of exothermic reactions
reactants → products + energy
Closed system
Surroundings get hotter, system’s temp decreased OR surroundings get cooler and system’s temp increased
In calorimetry… heat lost + heat gained =
0
Internal energy, U
= q + w
Enthalpy, H
heat only under constant pressure
In KJ/mole
= qp (subscript of p)
ΔH < 0
Exothermic
ΔH > 0
Endothermic
State function
Property or condition that relies only on the current condition, or state, that the object or system is in. How the object or system achieved that condition is reach is not relevant
Examples of state functions
temperature
Enthalpy
Pressure
Volume
Standard enthalpy of formation of an element in its most stable form
0 under standard conditions
Calculating ΔH for a reaction
ΔH = sum of ΔH(products) - sum of ΔH(reactants)
Hess’s law
If a process can be written as the sum of several stepwise processes, the enthalpy change of the total process equals the sum of the enthalpy changes of the various steps
Exothermic process turned around
Becomes endothermic
Conventions of thermochemical equations
If the coefficients of the chemical equation are multiplied by some factors, the enthalpy must also be multiplied by the same factor
2 perpendicular oscillating fields
Electric and magnetic
Wavelength
Distance from peak of one wave to peak of another wave
units of length
Frequency
How many wave forms are going to pass through in one second
units of hertz
Amplitude
How tall the peak is or how low the trough is
Independent of wavelength and frequency
Energy and frequency
Increase as you go up the light list
Wavelength (in accordance to the light lost)
Decreases as you go up the list
Harmonics
Integer multiples of the original ½ wavelength
Nodes
Divot the middle of the waves
One wave form
2 peaks and 2 troughs
Relationship between wavelength and frequency
Wavelength x frequency = speed of light ( c )
Radial nodes
Circles
Angular nodes
Radii
How we know light behaves like a wave
Diffraction as light passes through slits
Diffraction pattern
Some waves’ peaks combine and form an extra strong power, when the peak and trough interact, they cancel each other out
basis of classical mechanics
Experiments /observations that do not fit “light is a wave”
blackbody radiation
Photoelectric effect
Line spectra of atoms
Blackbody radiation
light from sun gives us a continuous spectrum
Approximated by blackbody radiation
Light given off by an object heated until it glows
The intensity should have kept rising, but it fell off, and that didn’t fit
Max Planck equation
E=hv = hc/wavelength
Particle nature of light
Photons
Albert Einstein’s first Nobel prize
Photoelectric effect
Photoelectric effect
Phototube with two electrodes that are not touching - closed circuit
when they shine light into the phototube, it produces a measurable current
Couldn’t explain that when using the purple/violet light they could see the current, but when they used red light they could not
Purple light had enough energy to knock the electron loose and produce the current
Einstein used collision to explain this and described light as a packet - energy depends on frequency or inversely on wavelength
Line spectra of atoms
If we have a source of white light that travels through and is split with a prism, we will get all the types of light within the white light
Bohr Model
occupy discrete energy levels and only exist in the available energy levels
May move between energy levels by either absorbing or emitting energy
Have energy levels designated by specific value for n
What the Bohr model gets right
electrons move between discrete energy levels
Accompanied by the absorption or emission of light whose energy corresponds to the difference in energy levels
Limitations of Bohr Model
works for H, and He, but not any other element
Relied on a precise orbit for the electron that is not correct
Electrons are…
Waves!
Wave function
3 dimensional stationary wave, psi
Psi²
Probability of finding an electron = orbital
can be used to determine the distribution of the electron’s density with respect to the nucleus in an atom
De Broglie Wavelength
Wavelength of matter (particles)
Wavelength of matter
h/mv = h/p
H = plank’s constant
M = particle mass
V = particle velocity
P = particle momentum
Heisenberg uncertainty principle
Use of wave functions
Can be used to determine the distribution of the electron’s density with respect to the nucleus in an atom
Quantum Theory of Electrons in Atoms
electrons in atoms can exist only in discrete energy levels but not between them
Energy of an electron in an atom is quantized
Energy can be equal only to certain specific values and can jump from one energy level to another, but not transition smoothly or stay between the levels
Quantum numbers
Mathematical solutions to Schrödinger equation
no 2 electrons in an atom have all the same quantum numbers
Principle quantum number, n
aka shell
Defines energy level
Size of the orbital
Describes how far away from the nucleus an electron is
Angular momentum, l
aka shape of the orbital
l = 0, 1, 2,
Max is n-1
l=0
S orbital
l=1
P orbital
l=2
d orbital
l=3
f orbital
S subshell
Spherical shape
P Subshell
Dumbbell shape
D and f orbitals
More complex
Orbital shapes
Represent the 3 dimensional regions where the electron is likely to be found
Radial nodes formula
n - l - 1
Nodes in a 1s orbital
1-0-1=0
Nodes in a 2s orbital
2-0-1=1
Nodes in a 3s orbital
3-0-1=2
Magnetic quantum number, m1
Orientation of the orbital in space
-l, … 0 …, +l
Spin quantum number, ms
Intrinsic property of electron
not a solution of wavefunction
2 possibilities for spin number
+1/2 (up) or -1/2 (down)
Pauli exclusion principle
an electron in an atom is completely described by 4 quantum numbers
No two electrons in the same atom can have exactly the same set of all four quantum numbers
Degenerate
Have the same energy
All energy units within 3p and 2p are the same energy
Shielding
Repulsion from inner electrons
electrons are attracted to nucleus but they are repulsed by each other
Effective nuclear charge
Z - shielding
Outer electrons have higher/lower energy
Higher - they are further from the nucleus
In any atom with 2 or more electrons…
The energy of the orbitals increase within a shell in the order s<p<d<f
Aufbau principle
Fill lowest energy orbitals first
Pauli exclusion principle
No two electrons have the same QN - 2 electrons per orbital
Electron configuration
The arrangement of electrons in the orbitals of an atom
3 pieces of information in an electron configuration
The principal quantum shell, n
The letter that designates the orbital type (l)
A subscript number that designates the number of electrons in that particular shell
Orbital diagrams
Pictorial representations of the electron configuration, showing the individual orbitals and the pairing arrangement of electrons
Hund’s rule
The lowest energy configuration for an atom with electrons within a set of degenerate orbitals is that having the maximum number of unpaired electrons
Two periodic table columns that have abnormal electron configurations
Group 6 and group 11
Electron configurations of anions
Electrons are added in the order predicted by the aufbau principle
Electron configuration of a cation
Add in electrons for neutral atom, then remove electrons
transition metals: remove a electrons before d