P - Atomic Structure Flashcards

1
Q

Electron configuration of Cr (Chromium)

A

1s²2s²2p⁶3s²3p⁶4s¹3d⁵ –> 6 unpaired e- –> more stable

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2
Q

Electron configuration of Cu

A

1s²2s²2p⁶3s²3p⁶4s¹3d¹⁰

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3
Q

Aufbau Principle

A

e- enter the lowest energy orbital possible.

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4
Q

Hund’s Rule

A

e- only pair up when no empty orbitals of the same energy are available.

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5
Q

Symbols of mass number and atomic number

A

Mass number (A) and atomic number (Z)

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6
Q

First ionisation energy

A

The energy required to remove 1 mole of electrons from 1 mole of atoms in the gaseous state.

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7
Q

Second ionisation energy

A

The energy required to remove 1 mole of electrons from 1 mole of gaseous 1+ ions.

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8
Q

Electron impact ionisation

A

Vaporised atoms are passed into a vacuum chamber,
where high energy electrons are fired at them,
knocking 1 electron from each of them to form a 1+ ion.

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9
Q

Electrospray ionisation

A

High molecular mass compounds are dissolved in water or a volatile solvent,
injected through a positively charged needle at high voltage,
the spray emerging with the solvent losing an electron to form a positive ion.

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10
Q

Isotopic abundances

A

The relative proportions of the stable isotopes of each element.

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11
Q

Give an example (formula) for first ionisation energy.

A

Na(𝗴) –> Na+ (𝗴) + e-
ENDOTHERMIC

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12
Q

Considerations for IE**

A
  1. size of nuclear charge
  2. distance of e- from nucleus
  3. shielding (by inner e- & nucleus)
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13
Q

Why is second IE higher than first IE?

A

First IE- removing e- from 𝙣𝙚𝙪𝙩𝙧𝙖𝙡 atom
Second IE- removing from 1+ 𝙞𝙤𝙣
𝙞𝙢𝙗𝙖𝙡𝙖𝙣𝙘𝙚: 𝙥𝙧𝙤𝙩𝙤𝙣𝙨 > 𝙚-
(∵ removed e-)

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14
Q

Describe the trend for first IE across the PERIOD.

A

Increases, as:
1. ↑ protons in nucleus
∵ ↑ nuclear charge
2. Atoms get smaller-
∵ ↑ force of attraction betw. nucleus & outer e-

(2 up –> 1 down)
Eg. Period 3
1. Al < Mg
∵ outer e- in 3p- 1. ↑ energy 2. further from nucleus
∴ ↓ energy to remove

  1. S < P
    ∵ 3p⁴ has 2 PAIRED e- ∴ repulsion- ↓ attraction to nucleus- ↓ energy to remove 1 from the pair than unpaired -easier =)

> increased shielding- negligible
∴ each successive e- enters same shell

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15
Q

Describe the trend for first IE down the GROUP.

A
  1. ↑ shielding
  2. ↑ distance from nucleus
    ∴ weaker attraction from nucleus to outer e-
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16
Q

How to determine what group the element it’s in from its successive ionisation energies?

A

Look for big jumps (eg. big jump from 2nd to 3rd –> group 2)
No apparent jump- group 0

17
Q

Why is it necessary to ionise atoms before acceleration?

A

Particles have to be charged before attraction to a charged plate/ electric field.

18
Q

What deflects ions in a mass spectromter?

A

Magnetic field.

19
Q

What is adjusted in order to direct ions with different m/z ratio onto the detector?

A

Magnetic field (/ strength of magnet)

20
Q

What accelerates positive ions before they are deflected?

A

Electric field.

21
Q

What factor, other than the mass to charge ratio of an ionised particle, determines how
much that particle is deflected in a magnetic field of a given strength?

A

Speed.

22
Q

Relative isotopic mass

A

Mass of the ISOTOPE relative to 1/12th the mass of an atom of Carbon-12.

23
Q

Isotopes of Cl

A

Cl-35 : Cl-37 = 3:1
m/z: 70 72 74
9 : 6 : 1

24
Q

What is the purpose of a detector in a mass spectrometer?

A

To detect POSITIVE IONS.

25
Q

Why do ions separate into different paths in a M. S.?

A

Diff. isotopes.

26
Q

For each type of ion, what 2 measurements can be made from the mass spectrum?

A
  1. m/z
  2. Abundance
27
Q

Formula of a ion
eg. C3H5O2N

A

C3H₆O2N+/ C3H5O2N𝑯+

28
Q

Write an equation for the electrospray ionisation of element X.

A

X (g) + H+ (g) –> XH+ (g)

29
Q

Write an equation for the electron impact ionisation of element X.

A

X(g) + e- –> X+(g) + 2e-

30
Q

How are particles accelerated in a mass spectrometer?

A

attracted to a -ve charged plate

31
Q

How many decimal places are included on low res mass spectrometry?

A

1

32
Q

How does high-res mass spectrometry allow us to identify compounds?

A
  • measured to 5 d.p.
  • see small diff. that low res x pick up
33
Q

When building a half equation, what is the first thing you balance?

A

species w/ variable oxidation state.

34
Q

After combining half equations, what should you remove?

A

spectator ions

35
Q
A