Chapter 7 Periodicity Flashcards

1
Q

How did Mendeleev organise his periodic table?

A

arranged using atomic mass and grouped elements that had similar properties.
–> If grouped properties did not fit, Mendeleev swapped elements around and left gaps, assuming the atomic mass measurements were incorrect

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2
Q

How is the modern Periodic table organised?

A

114 elements organised into 7 horizontal periods and 18 vertical groups
–> position is linked to physical and chemical properties
–> arranged in increasing atomic number

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3
Q

Groups and periods

A

vertical columns: groups which all have atoms with the same number of outer-shell electrons and similar properties

horizontal rows: periods
–> no on period gives number of highest energy electron shell in an element’s atom

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4
Q

Periodicity & properties

A

repeating trends in properties of elements
–> electron configuration
–> ionisation energy
–> structure
–> melting point

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5
Q

Trends across a period

A

Across period 2, 2s sub-shell fills with two electrons, then 2p sub-shell with 6 electrons e.g. Be is (He)2s^2 and Ne is (He)2s^2,2p^6

Across period 3 same pattern of filling for 3s and 3p sub-shells

Across period 4, although 3d sub-shell is involved, highest shell number=4 so from n=4, only 4s and 4p sub-shells are occupied

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6
Q

Trends down a group

A

Elements have the same number of electrons in each sub-shell (can be divided into 4 distinct blocks)
–> Group 1&2 are s-block
–> Group 3-12 are d block
–>Group 13-18 are p-block

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7
Q

Names and numbers of groups

A

1- Alkali metals
2- alkaline earth metals
3-12 Transition elements
15 pnictogens (N,P,As,Sb,Bi)
16 chalcogens (O,S,Se,Te,Po)
17 Halogens
18 Noble gases

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8
Q

Ionisation energy

A

How easily an atom loses electrons to form positive ions

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9
Q

First ionisation energy

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

Na(g) –> Na+(g) + e- //. X(g) –> X+(g) + e-

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10
Q

Successive ionisation of Chlorine

A

Cl(g) –> Cl+(g) +e- It is not diatomic because ionisation energy is from ONE atom at a time

IE2: Cl+(g) –> Cl2+(g) + e- (only one electron is removed per ionisation energy)

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11
Q

Factors that affect ionisation energy

A

Atomic radius, nuclear charge, electron shielding

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12
Q

Atomic radius IE

A

The greater the distance between the nucleus and outer electrons, the less nuclear attraction
–> force of attraction falls of sharply with increasing distance so atomic radius has a large effect

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13
Q

Nuclear Charge IE

A

More protons in nucleus= greater attraction between nucleus and outer electrons

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14
Q

Electron Shielding IE

A

Inner-shell electrons repel outer-shell electrons and reduces the attraction between the nucleus and outer electrons

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15
Q

Why is the second ionisation energy greater than the first IE?

A

Once an electron is lost, the single electron is pulled in closer as there are now more protons than electrons.
–> causes a stronger attraction on the remaining electron

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16
Q

Second ionisation energy definition

A

the energy required to remove one electron from each ion in one mole of gaseous 1+ ions of an element to form one mole of gaseous 2+ ions

17
Q

What does a large difference in ionisation energy mean?

A

This means a different shell is now losing electrons
–> much closer to the nucleus so stronger attraction
–> more energy is required to lose the electrons)

18
Q

Trend in first ionisation energies

A

As you go across each period, there is a general increase in first IE
–> higher nuclear charge= more protons in nucleus= more attraction between nucleus and outermost electron

A sharp decrease between end of one period and start of another ( He->Li/ Ne->Na/ Ar->K)

19
Q

As you go down a group, why does first IE decrease?

A

atomic radius increases
more inner shells in total so shielding increases (More repulsion)
nuclear attraction on outer electrons decreases
first ionisation energy decreases

20
Q

Trends in First IE across a period

A

Across a period, the nuclear charge increase as there are more protons
–> same shell means similar shielding levels
–> nuclear attraction increases and atomic radius decreases
–> first ionisation energy increases

21
Q

Why does Beryllium have a higher ionisation energy than Boron

A

Beryllium has no 2p subshell but Boron has one electron in the 2p sub-shell.
2p sub-shell in boron has a higher energy than 2s sub-shell in beryllium.
–> Therefore, in boron, the 2p electron is easier to remove than one of the 2s electrons in beryllium (lower ionisation IE)

22
Q

Why does oxygen have a lower ionisation energy than nitrogen

A

Due to electron pairing in p-orbitals of 2p sub-shell
–> in N & O, the highest energy electron are in a 2p sub-shell
–> in oxygen, paired electrons in one of the 2p orbitals repel one another, making it easier to remove an electron from an oxygen atom than a nitrogen atom
–> ionisation energy of oxygen is less than nitrogen

23
Q

Nitrogen and Oxygen electron configuration

A

3 2p electrons: 2px1 2py1 2pz1
–> one electron in each 2p orbital
–> spins are at right angles - equal repulsion as far apart as possible

4 2p electrons: 2px2 2py1 2pz1
–> two electrons in one 2p orbital
–> 2p electrons start to pair
–> paired electrons repel

24
Q

Metallic bonding and structure

A

in solid metal structure, each atom has donated its negative outer-shell electrons to a shared sea of electrons. (delocalised)
–> positive ions ( cations) left behind consist of nucleus and inner electron shells of metal atoms

Metabolic atoms: strong electrostatic forces of attraction between cations and delocalised electrons
–> fixed cation with mobile delocalised electrons
(giant metallic lattice)

25
Q

Properties of metals

A

strong metallic bonds
high electrical conductivity
high melting and boiling points

26
Q

Electrical conductivity

A

metals conduct electricity in solid and liquid states
–> voltage applied across metal= delocalised electrons can move through the structure, carrying charge
–> ionic compounds cannot carry charge when solid

27
Q

Melting and boiling points

A

depends on strength of metallic bonds in a giant metallic lattice
–> most require high temps to provide large amount of energy needed to overcome strong electrostatic attraction between cations and electrons
–> strong attraction results in most metals having high melting and boiling points

28
Q

Solubility

A

metals do not dissolve (can interact in a polar solvent)

29
Q

Giant covalent structures

A

strong network of covalent bonds
–> carbon and silicon both have 4 electrons
–> can form 4 covalent bonds to other carbon or silicon atoms (results in tetrahedral shape)
–> 109.5 bond angle

30
Q

Properties of giant covalent structures

A

melting and boiling points: high due to strong covalent bonds (need lots of energy to break)

solubility: insoluble as covalent bonds are way too strong to be broken by interaction with solvents

electrical conductivity: non conductors, except graphene and graphite
- in diamond all 4 electrons are used

31
Q

periodic trend in melting points

A
  • Melting point increase from group 1-14 (giant structures)
  • sharp decrease in melting point from group 14-15 (simple molecules)
  • melting points are comparatively low from group 15-18
32
Q

Bond strength

A

Giant covalent> Giant metallic> simple molecular

simple molecules: weak London forces between molecules