Unit 2: VSEPR theory Flashcards

i ALWAYS forget about whether it's VSEPR or VESPER or VESPR or...

1
Q

VSEPR theory

A

Valence shell electron pair repulsion theory

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2
Q

Atomic radius

A

Atomic radius: 1/2 the distance between the nuclei of two identical atoms in an element or compound
- Within a group -> atomic radii increase as you go down a group, as outer electrons occupy higher # (and energy) sublevels, farther away from the nucleu
- Within a period: atomic radii decrease across a period; added electrons are in the same energy level, and ^protons means a stronger pull on the electrons in that energy level, thus pulling them in tighter
- Measured in picometers (1pm = 10^-12m)

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3
Q

Shielding (IB key term)

A

Shielding: when electron shells prevent 2 atoms from bonding (electrons repulse each other; making it harder for them to come together to bond)
- Larger ring / more shells -> more shielding
- Stays relatively constant across a period, as # shells stays the same while ^atomic #

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4
Q

Ionic radius

A

Ionic radius: the distance between the nucleus of an ion to the outermost shell
- As electrons are in orbits, the more electrons there are, the larger the ionic radius
- Largest -> smallest radius: anion, neutral, cation
- Decreases across period (L -> R), as ^#protons
Increases as you go down a group, as atoms ^larger

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5
Q

Effective nuclear charge

A

Effective nuclear charge: as an atom has more protons, there is more โ€œpullโ€ so electrons are closer to the nucleus; increases L -> R

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6
Q

Electronegativity

A

Electronegativity: ๐“ฌ๐“ฑ๐“ฎ๐“ถ๐“ฒ๐“ฌ๐“ช๐“ต ๐“น๐“ป๐“ธ๐“น๐“ฎ๐“ป๐“ฝ๐”‚ ๐“ฝ๐“ฑ๐“ช๐“ฝ ๐“ญ๐“ฎ๐“ผ๐“ฌ๐“ป๐“ฒ๐“ซ๐“ฎ๐“ผ ๐“ฝ๐“ฑ๐“ฎ ๐“ฝ๐“ฎ๐“ท๐“ญ๐“ฎ๐“ท๐“ฌ๐”‚ ๐“ธ๐“ฏ ๐“ช๐“ท ๐“ช๐“ฝ๐“ธ๐“ถ ๐“ธ๐“ป ๐“ช ๐“ฏ๐“พ๐“ท๐“ฌ๐“ฝ๐“ฒ๐“ธ๐“ท๐“ช๐“ต ๐“ฐ๐“ป๐“ธ๐“พ๐“น ๐“ฝ๐“ธ ๐“ช๐“ฝ๐“ฝ๐“ป๐“ช๐“ฌ๐“ฝ ๐“ฎ๐“ต๐“ฎ๐“ฌ๐“ฝ๐“ป๐“ธ๐“ท๐“ผ ๐“ฝ๐“ธ๐”€๐“ช๐“ป๐“ญ๐“ผ ๐“ฒ๐“ฝ๐“ผ๐“ฎ๐“ต๐“ฏ (๐“”๐“ท)
- As you go across the periods and up the groups, the electronegativity increases
- Increased atom size and decreased effective nuclear charge
- Small peak in the middle of transition metals
- Fluorine is the most electronegative element
- Has a value of four, therefore all elements calculated relative to fluorine

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7
Q

Ionisation energy

A

Ionisation energy: energy needed for removal of the loosest electron that is being held from an atom in the gaseous state
- The stronger the attraction between valence electrons and the nucleus, the higher the ionisation energy
- Across the period -> increase in ionisation energy
- Atomโ€™s radius decreases as we go to the right
- Ionisation energy decreases as we go down a group because the valence electron(s) are further away from the nucleus; thus, hold on the valence electrons becomes weaker

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8
Q

Electron affinity

A

Electron affinity: the energy released when an atom gains an electron
- X(g) + eโป -> Xโป(g) + energy
- Electron affinity decreases as we move down a group because the radius of the atom is larger, making the distance between the electron on the valence shell and the nucleus larger, resulting in a weaker attraction
- ^Electron affinity as we move across a period due to the atomic radius decreasing, making the distance between the nucleus and valence electrons smaller, resulting in a stronger attraction

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9
Q

Melting point

A

Melting point: the energy required to change the state of an ion from a solid to a liquid
- The change of state is caused because the energy is high enough to break the bonds of the atom. As such, atoms with stronger bonds (i.e. the ones in the middle) will not break as easily and have a higher melting point

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10
Q

Determining polarity

A

Type of bond, geometry of molecule
- 0, 0.3 -> non-polar covalent
- 0.3, 1.7 -> polar covalent
- 1.7, 4.0 -> ionic bond
- Linear, trigonal planar, tetrahedral, trigonal bipyramidal, octahedral, square planar

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11
Q

Non-polar vs polar molecules

A

Non-polar: no unshared e-pairs
- Central atom surrounded by identical atoms, all which have same electronegativities
Polar: unshared e-pair
- Central atom has at least 2 different atoms surrounding it (which have different electronegativities)

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12
Q

Ionic

A

Ion: an atom with an electrical charge
- Formed from attraction between cations, anions
- Achieves stable octet (eight valence electrons)

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13
Q

Covalent

A
  • Formed when atoms share electrons
  • Diatomic molecules: H2, N2, O2, F2, Cl2, Br2, I2
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14
Q

Metallic

A

Metallic bond: results from the attraction between positive metal ions and the surrounding sea of mobile electrons
- Metals give up electrons readily, but do not have high ENs necessary to attract electrons
- In a pure chunk of metal, valence electrons are delocalized: they do not have one single atom, but are free to move around
- V,Es are shared equally by all atoms, resulting in an electron sea

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15
Q

Dipole-dipole forces

A
  • Strongest intermolecular forces; attraction between polar molecules
  • Equal but opposite charges separated by a short distance create a dipole
  • Dipole arrow points towards negative pole (^EV atom), + tail points towards positive pole
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16
Q

Hydrogen bonding

A
  • Particularly strong type of dipole-dipole attraction; strongest of all intermolecular forces
  • Attraction between hydrogen atom bonded to a strong e-neg atom (N, O, F) and unshared pair of electrons on another strongly e-neg atom (N, O, F)
  • Attration usually represented by a dashed line
17
Q

Van der Waalโ€™s forces / LDF

A

Intermolecular attractions resulting from constant motion of electrons and the creation of instaneous dipoles and induced dipoles
- ^Electrons -> ^LDF
- Forces are very weak
- Act between all molecules; only intermolecular forces acting on noble gases, non-polar molecular compounds

18
Q

Crystal type: ionic

A

Lattice points: ions
Bonds between particles: ionic bonds (600-4000 kJ/mol)
Melting points: high
Electrical and thermal conductivity: low in liquids, high in solids
Ductility and malleability: brittle
Hardness: hard
Solubility: generally soluble in polar solvents
Examples: KCl, MgO

19
Q

Crystal type: covalent network

A

Lattice points: atoms
Bonds between particles: covalent bonds (300-800 kJ/mol)
Melting points: very high
Electrical and thermal conductivity: low (w/some exceptions)
Ductility and malleability: none
Hardness: very hard
Solubility: insoluble
Examples: diamond quartz (SiO2)

20
Q

Crystal type: metallic

A

Lattice points: cations
Bonds between particles: metallic bonds (50 -800 kJ/mol)
Melting points: high
Electrical and thermal conductivity: very high
Ductility and malleability: usually ductile, malleable
Hardness: hard
Solubility: insoluble
Examples: Cu, Pb

21
Q

Crystal type: covalent molecular (polar)

A

Lattice points: polar molecules
Bonds between particles: hydrogen bonding, dipole-dipole (5-50 kJ/mol)
Melting points: low-intermediate
Electrical and thermal conductivity: low
Ductility and malleability: fragile
Hardness: soft
Solubility: generally soluble in polar substances
Examples: NH3, CH3COOH

22
Q

Crystal type: covalent molecular (non-polar)

A

Lattice points: non-polar molecules
Bonds between particles: dispersion forces (0-5 kJ/mol)
Melting points: vv low
Electrical and thermal conductivity: vv low
Ductility and malleability: vv fragile
Hardness: vv soft
Solubility: soluble in non-polar, slightly polar substances
Examples: CO2, CH4