Exam 2 Flashcards

1
Q

principle quantum number

A

n = energy level of electron/orbital
positive integer

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2
Q

angular momentum quantum number

A

l = shape of orbital
l = 0, 1, 2, …, n-1

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3
Q

magnetic quantum number

A

mₗ = orbital orientation
mₗ = -l, …, 0, …, l

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4
Q

spin quantum number

A

mₛ = spin of specific electron
mₛ = ±1/2

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5
Q

letter names associated with l values
l = 0, 1, 2, 3, 4

A

l = s, p, d, f, g

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6
Q

sketch orbital:
n=1
l=0

A

1s
0 nodes - nucleus doesn’t count
sphere

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7
Q

sketch orbital:
n=2
l=0

A

2s
1 node - radial
hollow sphere

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8
Q

sketch orbital:
n=2
l=1

A

2p
1 node - planar
dumbbell shape

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9
Q

sketch orbital:
n=3
l=1

A

3p
2 nodes - 1 planar, 1 radial
dumbbell with 2 hats

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10
Q

sketch orbital:
n=3
l=2

A

3d
2 nodes - planar
4 leaf clover or dumbbell with donut

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11
Q

sketch orbital:
n=4
l=2

A

4d
3 nodes - 2 planar, 1 radial
4 leaf clover or dumbbell with 4 hats

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12
Q

Hund’s Rule

A

Electrons should be placed evenly across degenerate orbitals before doubling up.

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13
Q

Pauli’s Exclusion Principle

A

Every electron within an atom has a unique identity, as determined by its n, l, mₗ, and mₛ values.

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14
Q

Aufbau Principle

A

When determining which electrons are in which orbitals, start from the lowest energy possibilities (orbitals).

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15
Q

paramagnetic

A

there are unpaired electrons in the atom
net spin non-zero
affected by magnetic fields

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16
Q

diamagnetic

A

all electrons are paired within the atom
net spin = 0

17
Q

atomic radius
(definition and periodic trends)

A

half of the distance between 2 bonded of an element
decreases across periods
increases down groups

18
Q

effective nuclear charge
(definition and periodic trends)

A

strength of the pull of the nucleus on electrons
increases across periods
decreases down groups

19
Q

ionization energy
(definition, periodic trends, and first vs. second ionization energy)

A

the energy required to move a valence electron
increases across periods
decreases down groups
first vs. second….

20
Q

ionic bonds nomenclature
e.g. NaCl
e.g. MgSO₄
e.g. FeCl₃

A
  • metal (cation), then nonmetal (anion)
  • cation element name + anion with “-ide” ending
  • add roman numeral after cation if needed
    e.g. sodium chloride
    e.g. magnesium sulfate
    e.g. iron (III) chloride
21
Q

cation nomenclature
e.g. Al⁺
e.g. Fe³⁺

A

add “ion”
add roman numeral after element name if transition metal
e.g. aluminum ion
e.g. iron (III) ion

22
Q

monoatomic anion nomenclature
e.g. Cl⁻
e.g. O²⁻

A

add suffix -ide
e.g. chloride
e.g. oxide

23
Q

molecular compound nomenclature PREFIXES
1-10

A

1 = mono-
2 = di-
3 = tri-
4 = tetra-
5 = penta-
6 = hexa-
7 = hepta-
8 = octa-
9 = nona-
10 = deca-

24
Q

molecular compound nomenclature
e.g N₂O
e.g. ICl₃

A
  • less electronegative element first
  • add prefixes except for mono- on first element
  • add “-ide” suffix to last element
    e.g. dinitrogen monoxide
    e.g. iodine trichloride
25
Q

electronegativity
(definition, periodic trends, polarity of molecular compounds)

A

the ability of an atom to attract bonded electrons to itself
increases across periods
decreases down groups
polar bonds occur when there is an electronegativity difference – polar compounds exist when vectors don’t cancel

26
Q

Formal charge (in a Lewis structure)

A

Calculate formal charge by subtracting the number of valence electrons around it in a compound from its atomic number
- includes all lone pair electrons and half of all bonded electrons

Prioritize lowest formal charges on each atom and opposite charges next to each other

27
Q

Violations of octet rule (Lewis structures)

A
  • odd number of valence electrons –> free radical
  • incomplete octet –> usually caused by formal charge
  • expanded octet (period 3 or below) –> more electrons on central atom
28
Q

VSEPR
electron domain geometries and angles for 2-6 domains

A

2 domains = linear (180°)
3 domains = trigonal planar (120°)
4 domains = tetrahedral (109.5°)
5 domains = trigonal bipyramidal (120° and 90°)
6 domains = octahedral (90°)

29
Q

2 electron domains:
molecular geometries

A

2 bonding = linear

30
Q

3 electron domains:
molecular geometries

A

2 bonding = bent (<120°)
3 bonding = trigonal planar (120°)

31
Q

4 electron domains:
molecular geometries

A

2 bonding = bent («109.5°)
3 bonding = trigonal pyramidal (<109.5°)
4 bonding = tetrahedral (109.5°)

32
Q

5 electron domains:
molecular geometries + bond positions

A

2 bonding (axial positions) = linear (180°)
3 bonding (axial + one equatorial) = T-shaped (90°)
4 bonding (axial + two equatorial) = seesaw (90° and <120°)
5 bonding = trigonal bipyramidal (90° and 120°)

33
Q

6 electron domains:
molecular geometries (start at 4 bonding)

A

4 bonding = square planar (90°)
5 bonding = square pyramidal (<90°)
6 bonding = octahedral (90°)

34
Q

valence bond theory
(2 types of bonds)

A

sigma (σ) bonds: head-to-head overlap –> single bonds
pi (π) bonds: side-to-side overlap –> double bonds

35
Q

valence bond theory
(significance of single, double, and triple bonds)

A

single bond = 1 σ bond
double bond = 1 σ bond and 1 π bond
triple bond = 1 σ bond and 2 π bonds

36
Q
A