Atoms, ions and compounds Flashcards

1
Q

Aufbau principle

A

electrons enter lowest energy orbital available

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2
Q

Hund’s rule

A

electrons prefer to occupy orbitals in their own and only pair up when no empty shells are availible

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3
Q

number of orbitals in sublevel s

A

1

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4
Q

number of orbitals in sublevel p

A

3

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5
Q

number of orbitals in sublevel d

A

5

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6
Q

number of orbitals in sublevel f

A

7

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7
Q

ionisation energy

A

energy required to remove an electron from its shell

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8
Q

Order electrons fill up shells

A

1s 2s 2p 3s 3p 4s 3d 4p

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9
Q

Isoelectronic

A

Species with the same electronic configuration

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10
Q

1st ionisation energy

A

Energy required to remove one electron from each atom in a mole of gaseous atoms producing 1 mole of 1+ gaseous ions

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11
Q

2nd ionisation energy

A

The energy require to remove the 2nd electron from each atom in a mole of gaseous atoms (starting with the 1+ ion)

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12
Q

3 Factors affecting ionisation energy

A
  • distance from nucleus (atomic radius)
  • nuclear charge
  • shielding
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13
Q

as you go down a group, 1st ionisation energy…. because….

A
  • decreases

- greater atomic radius, more shedding and less attraction between nucleus and electron

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14
Q

as you go across a period, 1st ionisation energy…. because….

A
  • increases

- more protons, same shielding, smaller atomic radius

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15
Q

2 dips in the ionisation trend (period)

A

group 2 to 3 (Mg, Al)

group 5 to 6 (P, S)

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16
Q

What causes the dip in the trend between Mg and Al

A

Al has a higher energy electron (3p) which is slightly further out so if lost more easily

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17
Q

What causes the dip in the trend between P and S

A

P has 1 electron in outer shell, S has 2 which repel each other and so lost more easily

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18
Q

degenerate orbitals

A

those with exactly the same energy

19
Q

principle quantum number

A

shall number

20
Q

shape of s-orbital

A

spherical - 2 electrons can be anywhere within the sphere

21
Q

shape of p orbitals

A

dumbell shaped - move anywhere within the shell

22
Q

4 stages of mass spectrometry

A

ionisation
acceleration
ion drift
detection

23
Q

2 main techniques of ionisation

A

electrospray ionisation

electron impact ionisation

24
Q

process of electrospray ionisation

A
  • sample dissolved in solvent
  • high voltage is applied
  • voltage rips an electron off the solvent and attached it to the sample molecules
  • creating positively charged ions
25
Q

main advantage of electrospray ionisation

A

doesn’t cause fragmentation

26
Q

typical uses of electrospray ionisation

A

polymers or biological materials - ie. DNA

27
Q

process of electron impact ionisation

A
  • sample is vaporised
  • and then hit with electrons from an electron gun
  • electrons knock electrons from molecules
  • forming positively charged ions
28
Q

process of acceleration of the sample

A
  • molecules are accelerated to the same kinetic energy
  • speed as different depending on the mass of the molecule
  • lighter particles have a greater velocity and so hit the detector plate first
  • lighter particles detected before heavier particles
29
Q

process of ion drift

A
  • time of flight = distance/velocity
  • ∴ time = distance x √ m / zKE
  • lighter ions take less time as time is dependant on √ m
30
Q

process of detection

A
  • ions hit negatively charged plate
  • causes a current, size of current gives a measure if the number of molecules hitting the plate
  • gives an abundance of the molecule
31
Q

x-axis of the spectrum

A

mass/charge ratio

32
Q

y-axis of spectrum

A

% abundance

33
Q

molecular ion peak

A

peak of greatest mass/charge ratio

34
Q

smaller peaks in spectrum are due to

A

isotopes of different masses ∴ different mass/charge ratios

35
Q

smaller, significantly lighter peaks due to

A

fragmentation of the molecule

36
Q

e. to find RAM of a substance using mass spectrometry

A

(isotope abundance % x isotope mass )/100

37
Q

2 exceptions of patter of loss of electrons from 4s before 3d

A

Cr - 4s1 3d5 - energetically favourable to have both half filled

Cu - 4s1 3d10 - energetically favourable to have 3d fully filled

38
Q

orbital

A

a region around the nucleus that can hold up to 2 electrons

39
Q

how do you determine the mass of an isotope

A

using a mass spectrometer

40
Q

how does a mass spectrometer work?

A
  • sample vaporised
  • then ionised to form positive ions
  • ions accelerated - heavier = slower + more difficult to deflect
  • ions detected on mass spectrum as a mass-to-charge
  • ratio is equivalent to relative isotopic mass
41
Q

how calculate mass-to-charge ratio?

A

mass of ion/charge of ion

42
Q

polyatomic ion

A

ion formed of atoms of more then 1 element bonded together

43
Q

binary component

- eg.

A

2 elements only

- sodium oxide