Unit 1 Flashcards

1
Q

frequency

A

peaks per second in hertz (Hz) or s^-1… variable is v

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2
Q

speed of light

A

assuming a vacuum for this course… variable is c

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3
Q

wavelength

A

length from peak/trough of wave. can be nanometers or meters for units (use 10^9/10^-9 as conversion)

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4
Q

Electromagnetic Radiation Spectrum

A

shorter wavelength, higher frequency, higher energy

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5
Q

c= v(lambda)

A
inversely proportional
c= speed of light constant
v= frequency (waves per second)
lambda= wavelength
- don't forget to convert wavelength to match units of light
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6
Q

energy levels

A

are called shells, orbits or symbolized by “n”. lower orbitals have less energy ex (n= 1 has less energy than n=4)

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7
Q

distance between energy levels

A
  • energy levels get closer together the further you go
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8
Q

electron goes down an orbital

A
  • electron loses energy so it will emit light of wavelength equal to energy lost
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9
Q

electron goes up an orbital

A

electron absorbs energy equal to wavelength of light given to it

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10
Q

absorption

A

electron goes up shell due to energy given to it

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11
Q

emission

A

electron goes down shell due to energy emitted

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12
Q

continuous spectrum of light (line spectrum)

A

shows rainbow

- all wavelengths on spectrum are visible light

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13
Q

emission lines (line spectrum)

A

few colours on a black backdrop visually
- the colours are wavelengths of light emitted when a gas atom was originally excited but that then electron emits the light was it goes back to rest state

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14
Q

absorption (line spectrum)

A

while light is going through a gas sample of an element, the electron would absorb some energy of that light causing

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15
Q

at what speed does all electromagnetic radiation move at?

A

the speed of light

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16
Q

electromagnetic radiation and energy transfer

A

ex. when molecules absorb radiation, it increases the energy of the molecules causing more collisions and a rise in temperature (case of microwave at least)

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17
Q

planck’s quantum theory

A

energy can only be gained or lost in whole number multiples of hv where h is a constant. can find energy absorbed or released

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18
Q

quantum

A

small packet of energy that can only occur in discrete units. system can only transfer energy in whole quanta thus energy seems to have particulate properties.

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19
Q

photosns

A

einstein discovered that electromagnetic radiation can be seen as a stream of particles called photons

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20
Q

delta e=nhv OR delta e=hc/(lambda)

A

gives the amount of a single quantum (the energy of a photon of light)

n= an integer
h= planck's constant
v= frequency
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21
Q

dual nature of light

A

electromagnetic radiation can show certain characteristics of particulate matter which is called dual nature

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22
Q

de Broglie’s equation

A

lambda= h/mv

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23
Q

lambda= h/mv

A

used to calculate the wavelength for a particle
- h=planck’s constant
m= mass
v= AHAH it is velocity

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24
Q

1 joule equals

A

1 kg times m^2 / s^2

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25
Q

hydrogen emission line spectrum

A

shows that only certain energies are allowed for the electron in the hydrogen atom AKA the energy of the electron in hydrogen is quantized. changes in energy between discrete energy levels in hydrogen will produce only certain wavelengths of emitted light. if any energy level was allowed, the emission spectrum would be continuous

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26
Q

emission spectrum

A

emission: when hydrogen molecules absorb energy and some of the bonds are broken. this results in excitation of electrons which means they contain excess energy which they release by emitting light of various wavelengths to produce the emission spectrum

contains black but with some colour bars in between

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27
Q

if energy levels in atoms were not quantized

A

all light would be white (contains all wavelengths)

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28
Q

delta e= -2.178 times 10^-18 J times z^2 (1/n^2f-1/n^2i)

A
n= integer. larger n is larger orbit radius
z= atomic number (usually 1 for hydrogen)
f= final
i= initial

this is negative when there is emission

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29
Q

e= -2.178 times 10^-18 J times (z^2/n^2)

A

gives the energy of each energy level

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30
Q

n=6 to n=1

A

n=1 has more negative energy because the electron in that level is more tightly bound to the smallest allowed orbit. the change in energy then is negative as energy is lost and electron is now in a more stable state. the energy is carried away from the atom by the production (emission) of a photon

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31
Q

bohr model

A
  1. model fits the quantized energy levels of the hydrogen atom and postulates only certain allowed orbits for the electron
  2. as electron becomes more tightly bound, its energy becomes more negative relative to the zero-energy reference state.
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32
Q

quantum model vs bohr

A

Bohr
Shells have set radii and electrons orbit the nucleus on those shell surfaces
Each energy level is a single shell
The shells surround the nucleus like planets surround the sun
Based on one number, the energy level, n

Quantum model
Each energy level is a collection of different orbitals/subshells (whose shape is defined by where you are most likely to find the electron 90% of the time)
Each orbital can hold 2 electrons
The orbitals have different complex shapes and electrons can travel anywhere within the space contained by the orbital
Each electron in an atom can be uniquely identified by 4 quantum numbers

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33
Q

quantum numbers

A

N
L
Ml
Ms
First three describe the orbital, the location of the electron
Last one describes the particular electron (spin number)

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34
Q

First Quantum Number, the principal quantum number

A

it is n (energy level)
n=1,2,3… (natural numbers, starting at 1)

N is the main factor in determining energy, it is not the only factor
Average distance from the nucleus (electron can literally be anywhere in orbital but mostly, on average, it stays at the n distance)
Higher n is more energy

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35
Q

Second Quantum Number, the secondary quantum number

A

it is l (orbital shape)
L (lowercase, cursive)= 0,…, (n-1) (whole numbers)

The “l” value represents a specific orbital shape/sub shell/ sub level
L = 0 → s orbital → sphere
L = 1 → p orbital → figure 8 or dumbell
L = 2 → d orbital → clover shape
L = 3 → f orbital → look up picture…
Possible values of L depends on which energy level you are looking at

Secondary factor of energy
Shape of orbital
Higher l is more energy

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36
Q

Which sub-levels (orbital shape) exists for the principal quantum numbers, 1-4?

A

Other levels do exist but there are the only orbital shapes that exist in ground state

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37
Q

Third Quantum Number, the magnetic quantum number

A

it is ml (orbital orientation)
Ml (lowercase m with lowercase l as subscript)= -l,…, l (integers)

Related to the orientation of the orbital in space relative to the other orbitals in the atom

Number of orbitals for that sublevel= number of orientation

___Letter equals orbital but don’t forget to say + and -!

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38
Q

interesting orbital energy thing

A

4s is lower in energy than 3d
Periodic table is organized in pdf where s can have 2 electrons therefore 2 columns, f can have 14 electrons therefore, 14 columns which is based on the ml number and its possible electrons per orbital

39
Q

Fourth Quantum Number, the spin quantum number

A

ms (spin)

In each sublevel (specific orbital), there are (up to) two electrons spinning in opposite directions
Whether electron is spinning clockwise or counterclockwise
ms= -½ or +½

*electron is a charged species which creates a magnetic field

40
Q

pauli exclusion principle

A

no two electrons can have the same set of 4 quantum numbers therefore only 2 electrons/ orbital

41
Q

aufbau principle

A

electrons will fill lowest energy orbitals first

  • lowest energy = ground state
42
Q

1s^1

A
1 = level
s= sublevel
^1= superscript of number of electrons in sublevel
43
Q

electron configuration and box diagram

A

the gap between the boxes show the differences in energy.

44
Q

hund’s rule

A
  • in a set of degenerate (same electron) orbitals, you will start by half filling the orbitals with electrons of the same spin
45
Q

shorthand notation

A

includes previous noble and gas place it in sir brackets (shows that it includes all electrons of that gas)
- can be used for box diagrams as well

46
Q

exceptions to octet rule

A

Be will be stable with 4 electrons since

B will be stable with 6 electrons

47
Q

when drawing a charged lewis structure

A

don’t forget to include formal charge/ square brackets and right amount of electrons

48
Q

expanded octets

A

remaining electrons are added to central atom. They are added to atoms past Phosphorus

49
Q

things that can explain polarity

A
  • shape does not determine polarity

- non polar and polar molecules may contain polar bonds/ lone pairs

50
Q

orientation of bonds and polarity

A

polar bonds on non polar molecule, they are on opposite sides of molecule
polar bonds in polar molecule, they are on same side of molecule

51
Q

orientation of lone pairs and polarity

A

lone pairs on non polar molecule, they are on opposite sides of molecule
lone pairs on polar molecule, they are on same side of molecule

52
Q

non polar molecules are

A

more symmetrical

53
Q

dipole moment is measured in

A

debyes or D

54
Q

bond angle for tetrahedral shape

A

109.5

55
Q

effect of lone pairs on angles in VSEPR

A

more repulsion and take up more space so pushes bonds downwards and decreases them by about 1 to 2 degrees

56
Q

5 VSEPR

A

trigonal bipyramidal

57
Q

6 VSEPR

A

octahedral

58
Q

5 with one lone pair VSEPR

A

see-saw

59
Q

5 with 2 lone pair VSEPR

A

bent

60
Q

5 with 3 lone pair

A

linear

61
Q

6 with one pair

A

square pyramidal

62
Q

6 with 2 lone pair

A

square planar

63
Q

resonance structure

A
  • when more than one possible lewis structure exists (by rotating pi bond around or lone pairs)
  • actual molecule is a hybrid of the lewis structures

Best: formal charge is on most electronegative atom

64
Q

benzene ring

A

draw a hexagon with a circle inside

65
Q

hybridization

A
  • occurs when the electron configuration does not match what the atoms oxidation state says
  • used to make bonds of equal energy level (pi bonds are higher energy)
  • when excited state, don’t forget to put a star
66
Q

hybridization and electron domain

A
2 --> sp
3 --> sp2
4-->sp3
5--> sp3d
6-->sp4d2
67
Q

pi bonds and hybridization

A

need at least 1 separate orbital with an electron inside of higher energy

68
Q

london dispersion

A
  • temporary dipole caused by another molecule coming close

- larger molecules are more stronger since there is more change of uneven distribution of charge at a single moment

69
Q

dipole dipole

A
  • permanent dipole

- more polar the molecule, stronger the forces

70
Q

hydrogen bonding

A
  • H and FON,
    due to small size and large electronegativity difference
  • lone pair is attracted to the slightly positive end of hydrogen
  • must have a lone pair on molecule
71
Q

melting and boiling point hydrogen bonding

A

high boiling point means large IMF since the bonds must be broken with tons of energy to boil (see picture)

boiling point increases as size increases due to dispersion

72
Q

viscosity hydrogen bonding

A

higher viscosity is high IMF since the molecules are more attracted to each other like honey with lots of glucose vs h2o

73
Q

surface tension hydrogen bonding

A

high IMF means high surface tension

tension at surface of a liquid

74
Q

force of attraction in ionic compound is

A

Called a crystal lattice

Attraction due to electrostatic forces of negative and positively charged ions

75
Q

Composition in ionic compound is

A

Network of ions

Formula is the ratio, not the number of atoms

76
Q

Strength - Coulomb’s Law

A

Coulomb’s law calculates the force of attraction based on charges
+1 ion vs +2 ion, +2 ion will have greater attraction

77
Q

Brittle (ionic compound)

A

Ions lined up perfect in an X and O pattern of anion to cation
When you take a hammer to an ionic compound, you shift the X and O pattern to be OXXO and XOOX (vs XOXO before) which creates large repulsion and it breaks

78
Q

Electrical Conductivity (ionic compound)

A

Ions are not mobile so they do not conduct electricity (electrons hop on mobile ions and then get to destination in water)
In solution, anions have extra electrons and are mobile so they conduct electricity

79
Q

What is the metallic bond?

A

When you take a metal like sodium (solid), you are looking at a bunch of sodium ions together
They create a sea of electrons where they each get rid of valence electrons and then the electrons just float around and go where needed (delocalized)
Matrix of positive nuclei in a sea of valence electrons

80
Q

What affects the strength of the metallic bond?

A

The number of delocalized electrons creates more valence electrons which makes more binding force so higher melting point???

81
Q

Electrical conductivity (properties of metals)

A

Since electrons are mobile and delocalized, can conduct electricity

82
Q

Malleability(properties of metals)

A

When you take a hammer to it, the positive nuclei simply shift down and the sea of electrons just surrounds in again
There is no repulsion so it does not break

83
Q

Low Volatility

properties of metals

A

The delocalization is very strong ??

84
Q

alloy

A

Mixture of metals (sometimes can be non-metal)

2 metals are melted, then mixed, then cooled

85
Q

Alloys vs metals

A

Different sized radius
Does allow/it is harder for nuclei to slide past another
Results in greater strength
Different metals add different properties

86
Q

covalent network

A

What is it?
A matrix where covalent bond holds atoms together
Covalent is very strong
Diamond (all sp3, tetrahedral)

also glass, SiO2

87
Q

properties of covalent network

A

Very hard/rigid
Extremely high melting point
Often in group 14 (carbon and silicon)

88
Q

Specific to Graphite structure

A

Structure: a network of c but hybridized sp2

Bunch of hexagons with 3 bonds per carbon
Flat (c is trigonal planar)
Multiple layers of carbon
No covalent bond between layers so attraction of layers is very weak (London dispersion)

89
Q

Specific to Graphite properties

A

Softer (layers can slide)

Conducts electrons through movement of electrons through resonance

90
Q

vapor pressure hydrogen bonding

A

is the pressure of air combined with the few molecules that tend to evaporate and go back into liquid form over any liquid
- lower IMF means it is easier to get into gas phase which increases the vapour pressure

91
Q

expanded octet

A

for third period atoms when there are too many electrons

92
Q

deficient octet

A

boron and beryllium due to electronegativity different. It is high enough to participate in covalent bonding

93
Q

formal charge

A

charge more than it should be on the atom