Topic 1 Atomic Structure & the Periodic Table Flashcards

1
Q

Relative Atomic Mass

A

The weighted mean mass of an atom of an element relative to 1/12 the mass of an atom of carbon 12.

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2
Q

Relative Isotopic Mass

A

The mean mass of an atom of an isotope relative to 1/12 of the mass of an atom of carbon 12.

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3
Q

Formula for RAM

A

Sum of (Mass of isotope x abundance of isotope) / total abundance of all isotopes.

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4
Q

Periodicity

A

Regularly repeating patterns across different periods/with increasing atomic number, e.g., in chemical , physical and/or atomic properties.

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5
Q

Describe the trend in melting point across period 3.

A

Increases: Na to Mg to Al. Metallic bonding: ionic radius decreases, protons & e- increase and attraction between the ions & e- increases.
Big jump to Si– giant molecular, lots of strong covalent bonds.
Big drop down to P4, slight rise to S8 and decreasing thereafter to Cl2 & Ar. All simple covalent molecules except Ar which is monoatomic with weak intermolecular forces.

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6
Q

d-block element

A

The last electron to fill an orbital does so in the d-subshell.

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7
Q

s-block & p-block elements

A

The highest-energy electron is found in an s-/p-orbital respectively.

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8
Q

Why don’t the d-block elements fit the same definition structure as p-block and s-block elements?

A

The 4s orbital e- has more energy than the 3d orbital e-.

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9
Q

Orbital

A

A region within an atom that can hold up to 2 e- with opposite spins.

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10
Q

In what order are e- lost?

A

e- further from the nucleus are lost first.

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11
Q

Filling of subshells

A

Singly first, then doubling up, so that e- in each orbital have opposite spins.

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12
Q

What determines the chemical properties of an element?

A

The number of electrons in the outer shell.

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13
Q

What’s so special about Cu and Cr?

A

They only fill the 4s1 orbital, not 4s2 like all the other elements in their period. This pattern is repeated periodically for Mo & Ag too!

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14
Q

Filling diagram

A

1s
2s 2p
3s 3p 3d
4s 4p 4d 4f
5s 5p 5d 5f
6s 6p 6d
7s etc.

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15
Q

Graph of 1st IE against atomic number for periods 1 & 2

A

Big jump from H to He then a huge drop down below H to Li.
1st IE increases from Li to Ne: the shielding remains the same, but the number of protons increases, so the attraction between the nucleus & outer electrons increases.

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16
Q

What are the exceptions to the trend in increasing 1st IE across period 2?

A

B & O.
B: less energy to remove the e- as it’s alone in the p-orbital, which has more energy than an s-orbital and is shielded by e- in the full s-subshell. A similar trend applies to Al concerning 3p.
O: 2p4, the 2 e- in the same orbital repel, so less energy is needed to remove one. Similar applies to S.

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17
Q

Why does He have the highest 1st IE?

A

No shielding. Smallest atomic radius.

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18
Q

What does the big jumps on a 1st IE graph of an element indicate?

A

A shell change. e- are removed from a shell closer to the nucleus that experiences less shielding.

19
Q

Why do successive IEs increase for an element?

A

The number of protons is the same, but the e- get closer to the nucleus.

20
Q

Isotopes of the same elements have identical chemical properties. Why?

A

They have identical electronic configurations.

21
Q

What is the difference between mass number & relative isotopic mass?

A

Mass number is always a whole number as it’s the sum of protons & neutrons in the nucleus) whereas relative isotopic mass is relative to the 1/12 the mass of an atom of carbon-12, so not likely to be an integer.

22
Q

Describe the mass spectrum of chlorine.

A

2 peaks at 35 & 37 with relative heights of 3:1. 3 peaks at 70, 72 & 74 with relative heights 9:6:1. Peak heights won’t be exactly 9:6:1 (as relative isotopic masses are not integers).

23
Q

What is the M + 1 peak?

A

In organic compounds, there is always a small % of the carbon-13 isotope present. the peak is only present/significant in molecules with large masses where the % of C-13 becomes significant.

24
Q

Molecular ion peak

A

The peak with the highest m/z ratio in the mass spectrum, the M peak.

25
Q

Quantum shell

A

Defines the energy level of an electron.

26
Q

Orbital

A

Region within an atom that can hold up to 2 electrons with opposite spins.

27
Q

Hund’s rule

A

Electrons will occupy orbitals singly before pairing takes place.

28
Q

Pauli Exclusion Principle

A

2 electrons cannot occupy the same orbital unless they have opposite spins.

29
Q

1st quantum shell

A

Electrons here have the lowest energy for that element. Contains only one subshell: 1s.

30
Q

2nd quantum shell

A

Two subshells: 2s & 2p.

31
Q

3rd quantum shell

A

3 subshells: 3s, 3p & 3d.

32
Q

4th quantum shell

A

4 subshells: 4s, 4p, 4d & 4f.

33
Q

How many orbitals in the s subshell?

A

1 (,so holds 2 e-).

34
Q

How many orbitals in a p subshell?

A

3 (, so can hold 6 electrons). The 3 orbitals are arranged at mutual right angles.

35
Q

Describe the shape of p orbitals?

A

Elongated dumbbell shape with variable charge density. The only difference between the 3 orbitals is their orientation in space.

36
Q

How many orbitals in a d subshell?

A

5, so can hold 10 electrons.

37
Q

How does atomic emission spectra provide evidence for the different energy levels in which electrons can exist within atoms?

A

When electrons in atoms are excited then return to ground state, they release electromagnetic radiation. All atoms of a particular element radiate the same specific set of frequencies, hence electrons can only have certain, fixed values.

38
Q

First ionisation energy

A

The energy required to remove one electron from each atom in one mole of atoms in the gaseous state.

39
Q

Second ionisation energy

A

The energy required to remove one electron from each singly-charged, positive ion in one mole of positive ions in the gaseous state.

40
Q

3 factors affecting ionisation energy

A
  • The orbital in which the electron exists
  • The nuclear charge of the atom.
  • The repulsion/shielding experienced by the electron.
41
Q

Trend in ionisation energy down group 1.

A

Down the group, nuclear charge increases with the increasing no. of protons, so the attraction between the nucleus and outer electrons increases. However, quantum shells are added down the group, which means there is more shielding and shells further from the nucleus are at higher energy levels than shells closer to the nucleus. The increasing nuclear charge is outweighed. First IE decreases down the group.

42
Q

Atomic radius

A

Distance between 2 nuclei / 2. The largest of these measures is Van der Waals’s radius; you can also measure covalent radius and metallic radius. Always compare like for like.

43
Q

Why does atomic radius decrease across periods 2 & 3?

A

No. of protons increases, so does nuclear charge. This increases the attractive force between the nucleus and outer electrons, which outweighs the slight increase in shielding due to additional e-.