Unit 3: Atomic Structure Flashcards

(57 cards)

1
Q

Rutherford:

A

Gold foil experiment w/alpha particles.

An atom consists of e moving around a dense + charged nucleus containing p.

Issues: e are constantly accelerating so they should eventually lose E and collapse into the nucleus.

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2
Q

Max Planck:

A

Analyzed blackbodies. He concluded that E is NON-continuous.

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3
Q

Blackbodies:

A

able to absorb/emit light @ a certain wavelength based on temp.

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4
Q

Quantum:

A

Small, discrete, indivisible quantity (burst = quantum of E)

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5
Q

Photoelectric effect:

A

ejection of an e can only happen when a min amnt of E from a photon is transferred to the e.

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6
Q

Photon:

A

Small packet of light E of a SPECIFIC frequency.

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7
Q

Bhor’s model:

A

e orbit nucleus in defined E states –> don’t collapse into nucleus. e can change their E by transitioning from on E state to another. so… e can only have certain allowed values –> quantized! Based his model on line spectra of H+.

LIMIT: Couldn’t explain line spectra for elements other then H+.

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8
Q

Louise de Broglie:

A

Stated that all matter has wavelike properties (found that the radius of orbit = # of wavelengths)

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9
Q

Erwin Schrodinger:

A

used math to explain that electrons have wavelike natures. Suggests that emission spectra results from e TRANSFORMING from one orbital to another.

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10
Q

Atomic orbital:

A

Predict the space where there is a high probability of finding an e in an atom = quantum mechanical atomic model.

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11
Q

Uncertainty principle (heisenberg):

A

position and speed of e cant be known w/certainty.

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12
Q

electron configuration:

A

e are arranged based on E lvls (don’t occupy orbits but ORBITALS)

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13
Q

n = principal

A

describes size. MAX amount of e in E lvl = 2n^2

Look at the e and the element, and based n on what period its in.

n = 1 @ ground state.

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14
Q

I = angular moment quantum number

A

describes shape. Values depend on n.

s-orbital: I = 0 (holds 2 e)
p-orbital: I = 1 (3 orbitals, w/2 e)
d-orbital: I = 2 (5 orbitals, w/2 e)
f-orbital: I = 3 (7 orbitals, w/2 e)

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15
Q

mi = magnetic quantum number

A

specifies orientation. depend on I.

draw orbital diagrams depending on the I value (like if I = 1, then its in the p orbital so 3 boxes) and draw arrows based on the configuration (so like if its 1s22s22p23s23p2, then it would have 2 arrows w/one in each box cuz 3p has 2)

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16
Q

ms = magnetic spin number

A

determines e spin. can be +-1/2

Based off of which direction arrow is in the orbital box drawing.

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17
Q

Pauli exclusion principle:

A

no 2 electrons can have the same values for n,I,mI,ms.

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18
Q

Aufbau Principle:

A

e are added to an atom one at a time; each to the lowest E orbital avail.

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19
Q

Shorthand e configurations:

A

Uses the preceding noble gas in place of the e configuration for the # of e in the noble gas.

EX:
Ar = 1s2 2s2 2p6 3s2 3p6
= [Ne] 3s2 3p6

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20
Q

Hunds rule:

A

the most stable arrangement of e in the same sub-shell has the max # of unpaired e w/same spin.

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21
Q

Expanded e configuration:

A

shows a list of EACH occupied orbital.

EX:
N = 1s2 2s2 2p3
N = 1s2 2s2 2p1 2p1 2p1

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22
Q

Orbital box diagram:

A

shows each occupied orbital and the e spins (arrows and boxes).

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23
Q

Exceptions w/transition metals:

A

contain occupied d orbitals filled AFTER the s orbital.

EXCEPTION:
- half fill or fill the (n-1)d orbital first, ns can be left HALF FILLED.

24
Q

Cations and Anions e config:

A

Cations: lose an e
EX: Li = 1s2 2s1
Li+ = 1s2 = [He]

Anions: gains e
EX: O = 1s2 2s2 2p4
O2- = 1s2 2s2 2p6 = [Ne]

25
Isoelectronic:
when e are added or removed such that a noble gas config is achieved.
26
ions w/multivalent atoms:
could lose e from s or last orbital EX: Pb can form Pb2+ (loses 6p2) or Pb4+ (loses 6p2 and 6s2)
27
Ferromagnetism: Fe, Co, Ni
Spins of e in a cluster of atoms align w/north poles in SAME direction. Acts like a magnet!
28
Paramagnetism:
Involves atoms w/unpaired e being attracted to a applied magnetic field. W/o applied field, thermal motion causes the spins to be randomly oriented.
29
Dimagnetism:
In atoms w/completely filled shells, all e spins are paired so no magnetism.
30
Core e and valence e:
CORE --> e filled in "inner" shells: those of the preceding noble gas. VALENCE --> e in the unfilled "outer" shells: additional e after the core ones (for first 3 periods) - for fourth period and below: the filled d sub-shells are ALSO apart of the core, even tho they aren't apart of the noble gas configuration.
31
Formal charge:
used to determine best charge for lewis structure: …the one with the fewest charges. …puts a negative charge on the most electronegative atom. SPLIT THE BOND and see how many e it has, then subtract from the actual e (based on periodic table) and see charge.
32
Resonance structure:
Group of lewis structures used to describe a molecule that cannot be accurately depicted using a single Lewis structure (RMBR to include arrows b/t the structures to show that they are isomers)
33
VSEPR:
Valence shell electron pair repulsion. Predicts the shape of molecules cuz e repel each other.
34
Bonding e and non-bonding e:
Bonding e = Valence e non-bonding e = lone pairs (shape affected by this cuz they use more space around the central atom so it changes e geometry to MOLECULAR geometry)
35
To predict VESPR shapes:
1. draw lewis 2. count bonds around central atom (DOUBLE, TRIPLE, etc count as ONE bond) 3. count any lone pairs on central atom 4. use sum of steps 2 and 3 to find electron geometry. also rmbr to include thetas to more electro- and electro+
36
If symmetrical vesper structure:
non polar (calculate en diff as well)
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If unsymmetrical vesper structure:
polar - not always polar tho (calculate en diff as well)
38
Intermolecular force:
forces b/t molecules --> det physical properties.
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Ionic forces:
Strongest IMF, caused by electrostatic forces that hold ions tg in ionic solids.
40
Dipole - dipole:
partial postive and partial - attract eachother.
41
H+ bonding:
special type of dipole-dipole attraction (FON)
42
Ion-dipole:
Ions can induce a dipole in non-polar molecules.
43
LDFS:
Weakest IMF. Exist in every molecule, caused by instantaneous dipole due to weak imbalance of e on one side of a molecule. - larger the size, greater the IMF (greater SA) - more irregular the molecule, weaker the IMF (less surface for interaction)
44
IMFS and solubility in h2o:
molecules have to be more attracted to other h2o molecules other then themselves in order to dissolve.
45
IMFS and electrical conductivity:
Ionic comps dissolved in h2o conduct electricity cuz of free ions. When electrodes are placed, the - ions will go towards cathode and + ions will go toward electrode.
46
Ionic Crystals:
Anions and cations are attracted together in CRYSTAL LATTICE.
47
Crystal Lattice:
A repeating pattern of ions in a crystal. Ionic substance held tg by STRONG electrostatic attractions in all three dimensions.
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Physical Properties of Ionic Compounds:
Hard, brittle crystalline solids, due to repulsion, have high melting and boiling points (due to strong IMFs), do not conduct electricity when solid – only when molten or in aqueous solution and are soluble in water.
49
Metallic Crystals:
A lattice of positive ions filled by a mobile ‘sea’ of valence electrons.
50
Physical Properties of Metals:
Attraction is between ions and mobile electrons: The layers of ions can slide past each other without breaking any bonds, are MALLEABLE and DUCTILE. They are good electrical conductors
51
Molecular Crystals:
covalent bonds result in molecules (I2, sulfur, ice, CO2) soft in solid state, do not conduct electricity, more soluble in non-polar solvent than in water, have low melting and boiling points.
52
Covalent Network Solids:
3D arrangement of covalent bonds between atoms that extends throughout a crystal. They are very hard, very high melting points, insoluble in water, nonconductors. Stronger than most ionic bonding
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ALLOTROPES
Different structural forms of an element
54
Diamond:
Each carbon is joined to 4 other carbons in the tetrahedral shape w/ an extremely strong structure! All made up of intramolecular bonds: Explains high MP, BP and exceptionally hard structure.
55
Graphite:
layers can slide over each other easily, conducts electricity: The electrons within them are free to move from one end of the sheet to the other end!
56
Fullerenes:
Behaves as an electron deficient molecule and readily accepts electrons: have a soccer ball structure w/lower MPs than diamond or graphite. Have small amnt of delocalized e but not enough to conduct electricity.
57
Silicon:
Forms 4 covalent bonds. Very similar structure to diamond.