atomic structure Flashcards

1
Q

Relative atomic mass

A

The average mass of an atom of an element compared to 1/12th the mass of an atom of carbon-12.

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2
Q

Relative isotopic mass

A

The mass of an atom of an isotope of an element compared to 1/12th the mass of an atom of carbon-12.

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3
Q

Relative molecular mass

A

The average mass of a molecule compared to 1/12th the mass of an atom of carbon-12

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4
Q

Mass number

A

The sum of neutrons and protons in an atom.

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5
Q

Atomic number

A

The number of protons in an atom.

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6
Q

history of atomic theory

A

dalton-stated that atoms are the smallest forms of matter
thompson- discovered electrons and proposed the plum pudding model which stated that atoms were a sphere of positive charge with electrons evenly distributed within it.
rutherford, geiger and marsden- conducted the alpha scattering experiment by firing alpha particles at a thin gold foil. mostly empty space as most particles went straight through, positive charge in the middle as some were deflected, small, dense nucleus as some bounced straight back.
bohr- proposed that electrons orbit the nucleus in shells.
chadwick-discovered neutrons

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7
Q

what is mass spectrometry

A

the mass spectrometer gives accurate information about relative isotopic mass and also about the relative abundance of isotopes.

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8
Q

what can mass spectrometry be used for

A

to collect data on the mass and abundance of elements

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9
Q

electron impact ionisation

A

-sample is vapourised, high energy electrons are fired at it
-the electrons are emitted from a charged hot wire filament
-the electrons knock off one electron from each particle, forming 1+ ions.
X(g) + e^- —> X^+(g) + 2e^-
-used for substances with low RFM
-the ions often fragments which may also be detected

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10
Q

electrospray ionisation

A

-the sample is dissolved in a volatile solvent and injected through a fine, positively charged hypodermic needle so it become a fine mist.
-the particles are ionised by gaining a proton from the solvent as they leave the needle, producing XH+ ions
X(g) + H^+ —> XH^+(g)
-the solvent evaporates away
-it is used for substances with higher RFM such as proteins
-fragmentation is rare

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11
Q

acceleration

A
  • the positive ions are accelerated so that they all have the same kinetic energyusing an electric field towards a negatively charged detection plate.
  • as the kinetic energy is the same, the velocity depends on the mass of the ions
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12
Q

drift

A
  • the positive ions travel through a hole in the negatively charged plate into a flight tube
  • the TOF depends on its velocity
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13
Q

detection

A

-Once they have pass through the mass spectrometer, the 1+ ions will hit a negatively charged ‘detector’ plate
-As they hit this electric plate, they gain an electron
which causes a current to be produced
-This size of the current is proportional to the abundance of the ions hitting the plate and gaining an electron
-The detector plate is connected to a computer, which produces the mass spectra.
- a spectrum shows the mass to charge ratio (m/z) and the abundance of each ion that reaches the detector.

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14
Q

why might there be a trace at half the expected m/z value

A

during the ionisation process, a 2+ ion may be produced so the m/z ratio is halved

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15
Q

define first ionisation energy

A

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

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16
Q

formulas for 1st 2nd and 3rd ionisation energy

A
1st:
X(g) --> X^+(g) +e^-
2nd:
X^+(g) --> X^2(g)+e^-
3rd:
X^2+(g) --> X^3+(g) + e^-
17
Q

factors affecting ionisation energy

A

proton number- more protons=stronger attraction between the nucleus and the outer e^-s.
atomic radius - smaller radius = outer e^-s are closer to nucleus so stronger attraction.
shielding - more inner electrons weakens the attraction between the nucleus and outer e^-s.

18
Q

why is IE always positive

A

-energy is always needed to remove an e^- from an atom as it is attracted to the positive nucleus.

19
Q

why is 2nd ionisation energy always bigger

A

the atoms becomes a positive ion so there is a stronger attraction between outer electrons and positive nucleus

20
Q

why can there be a big jump in IE

A

the next electron being removed is in the next shell which is closer to the nucleus.

21
Q

what are the periodic trends

A

atomic radii decreases as you go across a period. this is because the number of protons increases so the nuclear charge also increases. therefore, there is a stronger pull on the e- shells. ionisation energy increases across a period due to more protons but same shielding so stronger attraction between nucleus and outer e-s.

22
Q

what are the different subshells, how many orbitals do they have and how many e-s can they hold

A

S sub-shell has 1 orbital which holds 2 e-s
P subshell has 3 orbitals which holds 6 e-s
D subshell has 5 orbitals which holds 10 e-s
F subshell has 7 orbitals which holds 14 e-s

23
Q

why does the 4s subshell come before the 3d subshell

A

it has lower energy so fills first

24
Q

exceptions to the electronic configuration order

A

copper: 1s^2, 2s^2, 2p^6, 3s^2, 3p^6, 4s^1, 3d^10
chromium: 1s^2, 2s^2, 2p^6, 3s^2, 3p^6, 4s^1, 3d^5

25
Q

explain the group 2 to 3 dip in ionisation energy

A

the outer electron is being lost from the 3p subshell rather than 3s in magnesium. it is a higher energy shell so the e- is removed easier

26
Q

explain the 5 to 6 dip in ionisation energy

A

sulphur has paired electrons in the 3p subshell whereas phosphorous doesn’t. this causes electron-electron repulsion which decreases ionisation energy

27
Q

how does melting point change across a period

A

increases until group 4 and then decreases. metals on the left then covalent