3.1.1 Periodicity Flashcards

1
Q

First ionisation energy definition.

A

Energy required to remove one electron from each atom in one mole of gaseous atoms of an element to form one mole of gaseous 1+ ions.

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2
Q

How does atomic radius affect ionisation energy?

A

Greater the distance between nucleus and outer electrons, the less the nuclear attraction.

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3
Q

How does nuclear charge affect ionisation energy?

A

More protons in nucleus of an atom, greater the attraction between nucleus and outer electrons.
Therefore increased ionisation energy

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4
Q

How does electron shielding affect ionisation energy?

A

Shielding effect= inner shell electrons repel outer-shell electrons
Easier to lose outer electron, ionisation energy lower

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5
Q

Why would there be a large increase between 2 successive ionisation energies?

A

The second electron of the 2 is removed from an inner shell, which would take more energy.

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6
Q

What is the trend of first ionisation energies down a group and explain why.

A

Decreases down a group because
-atomic radius increases
-more inner shells, shielding increases
-nuclear attraction on outer electrons decreases

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7
Q

What is the trend of first ionisation energies across a period and explain why.

A

Increases because
-nuclear charge increases
-same shell, similar shielding
-nuclear attraction increases
-atomic radius decreases

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8
Q

Where is the s block on the periodic table

A

Two groups on the left

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9
Q

Where is the d block on the periodic table

A

Middle 10 groups

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10
Q

Where is the p block on the periodic table

A

Right 6 groups

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11
Q

Second ionisation energy definition

A

Energy required to remove one electron from each atom in one mole of gaseous 1+ ions of an element to form one mole of gaseous 2+ ions.

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12
Q

Metallic bonding definition

A

Strong electrostatic attraction between cations and delocalised electrons

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13
Q

Describe a giant metallic lattice

A

Billions of metal atoms held together by metallic bonding

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14
Q

Electrical conductivity of metals

A

Metals conduct electricity as when a voltage is applied across a metal, delocalised electrons can move through the structure and carry a charge

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15
Q

Melting and boiling points of metals

A

High
High temperatures needed to provide large amount of energy to overcome strong electrostatic attraction between cations and electrons

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16
Q

Solubility of metals

A

Do not dissolve

17
Q

What is a giant covalent lattice

A

Billions of atoms held together by network of strong covalent bonds

18
Q

Examples of giant covalent lattices

A

Carbon (diamond, graphene, graphite)
Silicon

19
Q

Structure of diamond and silicon

A

Have 4 outer electrons that form covalent bonds with other atoms, tetrahedral structure formed

20
Q

Structure of graphene

A

Single latter of graphite, hexagonally arranged carbon atoms linked by strong covalent bonds,
Bond angles of 120, 3 covalent bonds by each carbon

21
Q

Structure of graphite

A

Parallel layers of hexagonally arranged carbon atoms, layers bonded by London forces
3 covalent bonds formed by each carbon atom, spare electron is delocalised between layers, so conducts electricity

22
Q

Melting and boiling points of giant covalent lattices

A

High due to strong covalent bonds, lots of energy needed to break bonds

23
Q

Solubility of giant covalent lattices

A

Insoluble in most solvents, covalent bonds holding together atoms in lattice are too strong to be broken

24
Q

Electrical conductivity in giant covalent lattices

A

In diamond and silicon, all outer electrons are involved in covalent bonds, no mobile charge carriers
Graphene and graphite can conduct electricity

25
Q

What’s the trend in melting points across period 2 and 3 and explanation

A

Melting point increases from group 1 to 14, sharp decrease in melting point between group 14 and 15, melting points comparatively low from group 15 to 18

Sharp decrease due to switch from giant to simple molecular substances