Exam 3 Flashcards

1
Q

how are discrete line spectras produced

A

exciting a gas at a low partial pressure

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2
Q

formula for energy absorbed/emitted

A

hc/wavelength

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3
Q

quantized definition

A

a system is limited to specific energy values

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4
Q

when is a photon emitted

A

when an e- transitions from a ground state to an excited state

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5
Q

energy of a photon formula

A

h * v

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6
Q

relationship between electron energy and distance from nucleus

A

as one increases, so does the other

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7
Q

what is coulomb’s potential?

A

attractive force between a positive nucleus and an electron

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8
Q

important features of all orbital models

A

energies of electrons are quantized
electron energy increases with distance from nucleus
discrete energies (lines) in spectra come from quantized electronic energies

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9
Q

constructive intereference

A

peaks and troughs coincide to amplify

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10
Q

destructive interference

A

peaks and troughs conflict, cancels out

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11
Q

how to obtain probability density

A

square the wavefunction

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12
Q

principle quantum number

A

n
location of energy level/shell number

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13
Q

angular momentum quantum number

A

l
defines shape of orbital
any value from o to n-1

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14
Q

magnetic quantum number

A

m1
defines z component of l
ex. l = 1, m1 = -1, 0, +1

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15
Q

is absorption/emission of light endo or exothermic?

A

absorption: endothermic
emission: exothermic

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16
Q

wavefunction squaured …

A

probability of finding an electron at a given point near the position

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17
Q

radial distribution

A

total probability of finding an electron at a given distance (r) from the nucleus
- r increases with surface area

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17
Q

describe the electron density graph of the 1s orbital

A

starts high, goes lower, no nodes

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18
Q

describe the electron density graph of the 2s orbital

A

starts high, one node, one peak

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19
Q

describe the electron density graph of the 3s orbital

A

starts high, 2 nodes, one large peak, one smaller peak

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20
Q

describe the radial distribution graph of the 1s orbital

A

starts low, not at zero, one massive peak

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21
Q

describe the radial distribution graph of the 2s orbital

A

starts low, closer to zero, one node, two peaks second is larger than the first

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22
Q

describe the radial distribution graph of the 3s orbital

A

starts low, closer to zero, two nodes, three peaks getting progressively larger

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23
Q

orbitals in the nth energy level

24
#electrons in the nth energy level
2n^2
25
#orbitals in the l-subshell
2l + 1
26
how many electrons can each orbital hold
2
27
what is the pauli exclusion principle
no two e- can have the same set of 4 quantum numbers
28
what l values correlate to subshells?
l = 0, s l = 1, p l = 2, d l = 3, f
29
difference between surface nodes and radial nodes
surface nodes (planar) are found at the original of the radial graphs, while radial nodes are not
30
total nodes (surface + radial) =
n - 1
31
#surface/planar nodes =
l
32
diamagnetic definition
all e- are paired
33
paramagnetic definition
at least one unpaired e-
34
isoelectronic definition
same #e-
35
isovalent definition
same #valence e-
36
what are degenerate orbitals
having the same energy
37
what is effective nuclear charge
Zeff - strength of the e- – nucleus interaction - = Z (atomic number) - # core e- - increases from left to right - increases as electron subshell level decreases
38
what are the common periodic table trends
- atomic radii (size) increases from right to left and down - ionization energy (to remove an e- from a gaseous atom) increases left to right and up - electron affinity (energy change with addition of an e- to a neutral gas) more negative left to right and up - ionic radii --> anions are larger than cations
39
definition of electronegativity
the degree to which an atom can attract an e- in a bond
40
nonpolar covalent bond
equal sharing of e- between two identical nonmetal elements
41
polar covalent
unequal sharing of e- between two nonmetals small electronegativity difference
42
ionic
metal + nonmetal e- are transferred to nonmetal large electronegativity difference
43
as electronegativity increases, what happens to the following? - bond polarity - ionic character - covalent character
- increase - increase - decrease
44
what is bond order
essentially, number of bonds = # bonds/ # bond locations
45
as bond order increases, what happens to the following? - bond strength - bond length - bond dissociation energy
- increase - decrease - increase
46
what is formal charge
charge on an atom as determined by lewis dot structure = #valence e- - #e- shown around atom in lewis dot structure
47
what is needed for a lewis dot structure to contribute most in resonance?
- smaller (ideally 0) formal charges - more zeros for formal charges - if formal charges are equal, the structure with the more negative formal charge on the more electronegative atom
48
electron pair geometry versus molecular geometry
EPG: - geometry including all domains (including lone pairs) MG: - refers to actual arrangement of atoms - does not include lone pairs
49
what is a dipole moment? when does it cancel?
dipole moment: measure of molecular polarity - cancels when bond vectors cancel out --> nonpolar molecule - when bond vectors create a net vector --> polar molecule
50
relate VSEPR and polarity
(#atoms, #lone pairs) POLAR: (2,1) (3,1) (2,2) (4,1) (3,2) (5,1) NONPOLAR: (2,0) (3,0) (4,0) (5,0) (2,3) (6,0) (4,2) AND all atoms around central atom are the same
51
are hydrocarbons polar or nonpolar?
nonpolar
52
are binary atom molecules polar or nonpolar?
nonpolar
53
are X-Y molecules polar or nonpolar?
polar
54
where do sigma bonds lie
directly between the two nuclei of atoms
55
what type of bond is in all single, double, or triple bond?
sigma
56
compare sigma bonds and pi bonds
SIGMA - can rotate - symmetrical - stronger PI - cannot rotate - weaker
57
where do pi bonds lie
above and below the internuclear axis
58
what is required to make a pi bond?
two p-atomic orbitals