Topic 1: Atomic Structure and Periodic Table Flashcards

1
Q

Definition of relative atomic mass

A

The average mass of an atom relative to 1/12 of a C-12 Atom

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2
Q

Definition of relative isotopic mass

A

The average mass of an isotope relative to 1/12 of a C-12 atom

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3
Q

Definition of first ionisation energy

A

The energy needed to remove 1 mole of electron from 1 mole of gaseous atom

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3
Q

Definition of first ionisation energy

A

The energy needed to remove 1 mole of electron from 1 mole of gaseous atom to form 1 mole of gaseous +1 ion

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4
Q

Definition of successive ionisation energy

A

The energy needed to remove one mole of electron after another

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5
Q

What are ionisation energies influenced by?

A

Atomic Radius - Larger atomic radius = smaller I.E as the outer electrons are further from the nucleus so the attractive force from the nucleus is weaker

Nuclear Charge - Higher nuclear charge = higher I.E as there’s a greater positive charge in the nucleus so the attractive force is stronger felt by the electrons (Larger Proton to electron ratio)

Shielding - More shielding = smaller I.E as the inner shells repel the electrons in the outer shells

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6
Q

Definition of effective nuclear charge

A

The sum of protons - the sum of shielding electrons

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7
Q

Why does first I.E generally increase across the period?

A

Same period = Same number of shielding electrons, but the nuclear charge increases. Effective nuclear charge would increase. The P/e- ratio stays the same. So each electron would feel a greater force of attraction to the nucleus so I.E would increase.

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8
Q

When are the two decreases in I.E across the period?

A

Between s2p0 and s2p1 - The s2p1 is lower because further from nucleus and more shielded

Between s2p3 and s2p4 - one electron in each p orbital in group 5 while there’s one pair of e- in an orbital in group 6 so the repulsion makes the I.E lower

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9
Q

Why does the first I.E decrease down the group?

A

The same number of e- in the outer shell but more shielding e-. So larger atomic radius —> less attraction between e- and the nucleus and greater shielding effect

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10
Q

Describe the shape of an s and p orbital

A

S orbital - spherical
P orbital - dumbbell shaped (infinity shape)

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11
Q

What are the number of electrons that can fill and s, p and d orbital?

A

S - 2
P - 6
D - 10

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12
Q

What are the trend of successive ionisation energies?

A

Successive I.E increase between shells. Sudden rise in I.E after each shell as shielding e- decrease suddenly and so effective nuclear charge increases. Smaller atomic radius

Successive I.E increase within each shell. Larger P/e- ratio so more attraction between nucleus and e- and less repulsion between e-

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13
Q

Periodicity Trends

A

Atomic radius decreases —> same number of shells but more protons so stronger attraction between outermost e- and nucleus

Melting point trend according to structure -
Increase in metals with metallic bonding as smaller radius and more delocalised e- present
Giant covalent structure = highest m.p

Simple covalent molecules —> similar m.p

Monoatomic= lowest m.p

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