Atomic structure and emission spectra Flashcards

1
Q

Isotope def

A

Different versions of an element with the same number of protons but different number of neutrons

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2
Q

Relative isotopic mass

A

Mass of a particular isotope of an element relative to one twelfth of mass of carbon-12.

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3
Q

Relative atomic mass

A

Weighted average of all naturally occurring isotopes of an element relative to one twelfth of mass of carbon 12.

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4
Q

First ionisation energy def

A

Energy required to remove one mole of electrons from one mole of gaseous atoms.
M(g) -> M+(g) + e-

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5
Q

2nd ionisation energy etc.

A

Energy required to remove one mole of electrons from one mole of 1+ (and etc.) gaseous ions.

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6
Q

Things that govern ionisation energy

A

Nuclear charge

Electron shielding, electron shielding is a much more significant factor than nuclear charge.

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7
Q

Why does first ionisation energy decrease down group 1?

A

Despite nuclear charge up, number of shells up, meaning more shielding between nucleus and outer electron and less effective nuclear charge so less energy required to remove it.

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8
Q

Why general increase in first ionisation energy across a period?

A

Nuclear charge increases with number of protons. Same shells therefore similar shielding.

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9
Q

How is atomic emission spectra made?

A

Made by exciting electrons via heat/electricity to excite them to higher energy level. As they go back down to lower energy levels, specific wavelengths of electromagnetic radiation is emitted and detected.

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10
Q

What does a line spectra prove?

A

That electrons can only exist at certain energy levels (shells) rather than any as only certain energy transitions are possible.

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11
Q

What is successive ionisation?

A

Sequential removal of all electrons surrounding an atom from highest energy level to lowest. Each electron removed requires more energy.

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12
Q

Why is successive ionisation energy much higher when going to a new shell?

A

Reduced shielding, Z eff increased, more attraction.

Also proof for shells.

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13
Q

How many orbitals in an s, p and d subshell?

A

1, 3, 5

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14
Q

Shape of each subshell

A

Google it

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15
Q

What is up spin?

A

+1/2 or half arrow upwards

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16
Q

What is down spin?

A

-1/2 or half arrow downwards

17
Q

What is orbital?

A

Region within an atom that can hold up to two electrons with opposite spins. 90% chance of finding electron inside.

18
Q

What is Hund’s rule of Maximum Multiplicity?

A

Electrons in the same subshell will fill all available orbitals singly before pairing in the same orbital as it minimises electron repulsion.

19
Q

Pauli’s Exclusion principle

A

No two electrons can have the same 4 quantum numbers and so if the electrons are in the same orbital, they must have opposite spin.

20
Q

Order that subshells fill

A

1s, 2s, 2p, 3s, 3p, 4s, 3d, 4p, order on periodic table

21
Q

Aufbau principle

A

Electrons must fill orbitals from lowest energy state - ‘ground state’.

22
Q

Electron config of Cr

A

[Ar] 4s1 3d5

23
Q

Electron config of Cu

A

[Ar] 4s1 3d10

24
Q

Why is the electron config of Cr and Cu different?

A

To reduce repulsion in the 4s shell, a 4s electron is promoted to the 3d subshell to create a half/fully filled shell which is at a lower energy state.

25
Q

Ionisation of transition metals

A

Remove 4s electrons first when ionising

26
Q

What part of an element determines its chemical properties

A

Electronic config

27
Q

Why does first ionisation energy decrease from Be to B despite nuclear charge increasing?

A

This is because the outer electron removed in B is from the 2p subshell and therefore has increased shielding from the 2s subshell electrons. Zeff is therefore lower and less energy is required to remove electron.

28
Q

Why does first ionisation energy decrease from N to O despite nuclear charge increasing?

A

The outer electron in O is paired in the 2p subshell whereas in N it is not. Therefore, there is increased electron repulsion and less energy is required to remove the electron.