Topic 4: Periodic trends and molecular orbital theory Flashcards

1
Q

What is nuclear charge and effective nuclear charge?

A
  • Nuclear charge: number of proteons in nucleus
  • Effective nuclear charge: partial nuclear charge felt by electrons in multi-electron atoms
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2
Q

Compare the effective nuclear charge on electrons that are closer and further from nucleus

A

Electrons closer to the nucleus are more strongly attracted to the nucleus, thus higher Zeff
Electrons further away from the nucleus or in outer orbitals are shielded by those closer –> weaker attraction and lower Zeff

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3
Q

Identify and explain the trend of effective nucler charge and atomic radii in the periodic table

A
  • Across the period:
    + same quantum number but the number of electrons in the outer orbital increases
    + orbitals of the same quantum number don’t shield effectively
    –> more affected by nuclear charge –> attracted more strongly to nucleus
    –> decreasing radii and increasing Zeff
  • Down a group:
    + increasing quantum number with same number of electrons in the outer orbital
    + orbitals of smaller quantum number shield those with higher quantum number effectively
    –> less affected by nuclear charge –> attracted less strongly to nucleus
    –> increasing radii and decreasing Zeff
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4
Q

Compare anionic and cationic radii with neutral atoms

A
  • Anionic radii:
    + anions are usually formed with electrons added to the same orbital
    + same Z and same Zeff
    –> more electrons means more electron repulsion
    –> larger radii (-2 also > -1)
  • Cationic radii:
    + electrons removed from outer orbital
    –> valence electrons closer to nucleus –> stronger Zeff
    –> smaller radii than neutral atoms
    –> cations usually are smaller than anions in ionic compounds
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5
Q

Explain ionisation energy (Ei) and compare Ei of atoms with larger or smaller Zeff

A

Ionisation energy is energy required to remove an electron completely from an atom.
–> energy input –> always positive

Larger Zeff –> strongly attracted to the nucleus
–> more energy required to remove electron
–> larger Ei

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6
Q

Identify and explain the trend of ionisation energy in the periodic table

A
  • Across a period: Zeff increases
    –> electrons tightly bound to nucleus –> more energy input to remove –> increasing Ei
  • Down a group: Zeff decreases
    –> electrons less tightly bound to nucleus –> less energy input to remove –> decreasing Ei
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7
Q

What is first ionisation energy and how is it compared to second ionisation energy?

A

Energy required to remove the first electron from a neutral atom
When 1 electron is removed, if there are still electrons in that orbital, then the electron repulsion is still less –> a bit more affected by Z –> higher 2nd Ei.
If after the 1st electron being removed, the outer orbital is empty, then outer electrons are closer to nucleus –> higher 2nd Ei

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8
Q

Explain electron affinity (Eea)

A

Energy change when an electron is added to an atom in the gas phase

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9
Q

What does it mean when energy is required or released when electron is added to neutral atoms?

A
  • Require energy input means the added electron needs to occupy higher energy level or it disrupts half-filled orbital
    –> atoms not have an affinity for electrons
  • Release energy output means the added electron occupy the same orbital with the valance electrons or fulfill the valence shell
    –> more stable
    –> the atom has affinity for electrons and has a negative Eea
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10
Q

Compare the ionisation energy and electron affinity between metals and non-metals

A
  • Metals have a very low ionisation energy as they want to lose rather than gain electrons
  • Non-metals have an affinity for electrons as they readily gain electrons to fulfill valence shell.
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11
Q

Explain how electron sharing leads to lowering of energy in terms of
i) de Brogile wavelength
ii) attraction and energy level

A

i) When atoms come together, electrons are shared in between the nuclei -> increased wavelength -> decreased energy

ii) When 2 atoms come together, they share electrons in the area in between the two nuclei. This is a covalent bond so the attraction between nucleus and the new electron is stronger than the repulsive force. As electrons are now affected by more electrostatic attarction than usual, their energy lower down.

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12
Q

Explain how the distance in between 2 atoms affect their interaction, overall energy and stability
Explain bond length and bond energy

A
  • Atoms of different elements will have different distances at which they display no interaction or start attracting.
  • When 2 atoms are too far apart, they exert no attraction towards each other –> total enegry is the sum of 2 individual atoms
  • Bond energy:
    + the energy difference between individual atoms and the molcule; or
    + the energy required to break the bond of the molecule
  • As the distance gets smaller, the 2 atoms start to attact, energy level decreases and the atoms become more stable
  • Bond length: the distance at which
    + the molecule has the most stable balance between attractive and repulsive forces; if lower, repulsive forces overwhelm
    + the molecule has the most energetic advantage over individual atoms
    + the new molecule is at the lowest energy position
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13
Q

What is the unit of distance when discussing atomic distances?
What is the equilibrium bond length?
What is Bohr radius?

A
  • Unit: Ångström (Å)
  • Equilibrium bond length: ~1Å
  • Bohr radius: the most like distance between a proton and an electrons in a H atom - 0.53Å
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13
Q

How to determine the number of molecule orbitals in general?

A

Total number of atomic orbitals in component atoms
= number of molecular orbitals

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14
Q

Explain how constructive and destructive interaction between orbitals result in molecule with higher and lower energy level compared to individual atoms

A
  • Same phase –> constructive interaction
    –> larger amplitude –> higher electron density in between the nuclei –> minimize internuclear repulsion
    –> Bonding molecular orbital
  • Different phase –> destructuve interaction
    –> smaller amplitude or cancel out
    –> lower or NO electron density in between the nuclei
    –> nodes appear and internuclear repulsion increases
    –> Anti-bonding molecular orbital with nodes
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15
Q

Identify the key difference between bonding and anti-bonding orbital

A

Anti-bonding MO always has nodes while bonding MO don’t have

16
Q

What happens to the energy level when both bonding and antibonding MO are fully filled?

A

When both bonding and antibonding orbitals are fully filled, there is no net energy gain from this interaction –> this interaction doesn’t occur.

17
Q

Determine the role of valence electrons in bonding and energy level

A

Only valence electrons determine bonding because the inner electrons have filled the MO and thus, cancel out.

18
Q

Explain the mixing of pi orbitals and resulting molecular orbitals

A
  • 1 pair of p-orbitals (pz) have end-on interaction
    –> sigma bonds
  • 2 other pairs of p-orbitals (px and py) have side-on interaction –> pi bonds
    –> 2 bonding and 2 anti-bonding MO
19
Q

How is the energy level of MO arise from side-on interactions compared to each other?

A

2 bonding and 2 anti-bonding pi orbitals have same energy level –> degenerate orbitals

20
Q

What is special about the order of energy level of sigman and pi bond in different elements?

A

The order of energy level of sigman and pi bonds may vary in different elements.

21
Q

Explain the difference between paramagnetism and diamagnetism

A
  • Paramagnetic molecules: have unpaired electrons –> able to move in magnetic field –> have net magnetic movement and be attracted
  • Diamagnetic molecules: NO unpaired electrons –> NO magnetic moment –> be weakly reprelled
22
Q

Describe the molecular orbitals in heteronuclear molecules

A

Heteronuclear molecules mean there are interactions between atoms of different elements with different nuclear charges
–> different energy levels even of the same atomic orbitals
–> unequal sharing of electrons –> asymmetric molecular orbitals

23
Q

What does it mean when orbitals are non-bonding?

A

If there is a large difference in the energy level between atomic orbitals, the orbital that is not close enough to any other orbitals of the atoms remain non-bonding and is distorted towards its own atom.

24
Q

Identify, describe and distinguish
i) polar and non-polar bonds
ii) dipole and dipole moment
iii) polar and non-polar molecules

A
  • Unequal sharing electrons between atoms due to difference in electronegativity and nuclear charge
    –> polar covalent bond
    –> electrons unevenly distributed –> slightly charged on both sides –> dipole moment (the more polar, the larger dipole moment
  • Equal sharing electrons due to NO difference in electronegativity
    –> non-polar covalent bond
  • Polar molecule: has net partial charge
    + can have ionic or polar covalent bond
    + a molecule with 2 poles is called dipole
    + have dipole moment that not cancel out
  • Non-polar molecules: no positve or negative poles; either
    + share electrons equally or
    + have polar bonds/dipoles but they cancel out
25
Q

What is HOMO, LUMO and HOMO-LUMO transition?

A

HOMO: Highest Occupied Molecular Orbital
LUMO: Lowest Unoccupied Molecular Orbital
HOMO-LUMO transition: lowest energy electronic transition of a molecule