3.1.1 atomic structure Flashcards

1
Q

history of the atom

A

lol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what happens when an e- gains/loses energy

A

when an e- gains energy it gets excited and moves to a higher energy level. when it loses energy it relaxes to its ground state

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

anion

A

+ve ion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

cation

A

-ve ion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

isotope

A

atom of an element with the same number of protons and a different number of neutrons

(you can have ions of isotopes)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

why do isotopes of they same element have the same chemical properties

A

because they have the same electron configuration/ number of e-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

why do isotopes of the same element have different physical properties

A

bc they each have a different number of neutrons.

isotopes with more neutrons have
1. higher mass
2. higher density
3. higher m/b points
4. slower diffusion rates

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

relative atomic mass

how is it calculated

A

average mass of an atom of an element to 1/12 the mass of a C12 atom

using abundance of isotopes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what is an energy level

A

specific orbits which electrons occupy as they orbit around the nucleus

each energy level represents a specific energy value

each energy level contains a different number of electrons

as you go further out energy values are higher

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is a sublevel

A

energy levels can be broken down into sublevels: s, p, d etc.
energy level one only has s
el 2 has s and p
el 3 has s, p, d

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is an orbital

A

sublevels can be broken down into orbitals. these are basically areas where electrons probably occupy. there are max 2 electrons in each orbital

the s sublevel has 1 orbital, so 2 e-
the p sublevel has 3 orbitals; 6
the d sublevel has 5 orbitals; 10

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

why does 4s fill before 3d

A

as we go further out from the nucleus the sublevels overlap more and more. 4s is actually of lower energy than 3d. according do Aufbau principle, electrons fill the lowest energy orbitals. once it fills it’s of higher energy.

the diagonal rule can be used to identify which sublevels come next

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

two types of representing electron configuration

A

standard

and short structure, where you use the nearest noble gas in square brackets then add the extra e-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what are two special cases of e- configuration

A

chromium

copper

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

special case of chromium

A

should be the standard configuration but instead it ends in
4s13d5

because electron is demoted from 4s to 3d because atoms are more stable with a half set of orbitals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

special case of copper

A

should be the standard configuration but instead it ends in
4s13d10

because electron is demoted from 4s to 3d as the atom is more stable with a full set of 3d orbitals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

ionisation energy

A

energy required to remove one mole of electrons from one mole of atoms in gaseous state

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

units of IE

A

KJmol^-1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

why is the reaction of IE endothermic

A

energy needs to be taken in by the outer e- being removed to overcome the eFoA between the nucleus and itself

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

def 2nd IE

A

energy required to remove one mole of electrons from +1 ions (!!) in a gaseous state

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

how can we quickly form the IE equation for different IEs?

A

nth IE ;

then the product of the reaction is +n charge

22
Q

why is 1st IE the lowest value always

A

eFoA is stronger in +ve ions compared to a less positive or neutral atom because there is more positive acting on the outer e-

each time requires more energy; you’re trying to remove from an increasingly +ve ion

23
Q

what are successive ionisation energies

A

they are the IEs (in KJmol^-1) to remove successive electrons from the same atom

results can be logged on a graph and conclusions have been made for it

24
Q

what can be observed from a graph depicting successive IEs?

A
  1. different electrons require different amounts of energy to be removed
  2. graph is not linear
  3. jumps in the graph (indicate energy levels)
25
Q

how do jumps in the successive IE graph show existence of energy levels

what do the gradual increase lines mean

A

in a jump from X to y, the y electron must be significantly closer to the nucleus bc there is a significant amount of energy it needs more than X electron.

expected bc ion is increasingly+ve

26
Q

how can you tell group number from successive IE data

how can you tell period number

A

identify big jumps in the numbers

group number = e- in outer energy level

however many electrons before 1st jump = group number

period number is no. energy levels.
n+1 rule: no. energy levels is the no. jumps add 1

27
Q

what happens to IE value down a group

A

it decreases

28
Q

what factors affect the strength of the eFoA between the nucleus and outer e-

A

nuclear charge

distance between the nucleus and outer e-; atomic radius

shielding

29
Q

why does IE decrease down a group

A

nuclear charge increases but this is offset by the
1. increase in atomic radius due to more completed energy levels making the electron further away from the nucleus therefore decreased FoA

  1. increase in shielding because there are more completed energy levels which weakens the FoA
30
Q

what does the trend of group IE decreasing show

A

probes that the outer e- as you go down must be further away and with more shielding

we would expect it to be greater and greater due to the increased nuclear charge. so the fact it decreases indicates the presence of energy levels, causing this effect of atomic radius and shielding

31
Q

what is the trend in IE across a period

A

it increases overall

32
Q

what is the reason for the trend in IEs across a period

A

there is a negligible increase in shielding because sublevels are being filled

there is an increase in nuclear charge so the eFoA increases, making the overcoming of that require more energy

there is a DECREASE in atomic radius because nuclei are better at attracting e-s (more protons). so increased FoA; the e- cloud is slightly closer.

33
Q

where are the deviations from the overall trend in IE across a period

why?

A

groups 2 -> 3
outer e- is being removed from an orbital of higher energy (be specific in questions) so less energy is needed to remove it.

groups 5 -> 6
there is a pairing of e-s in the orbital of gr6 atoms where there isn’t in gr5. so electron repulsion. less energy needed to remove it

34
Q

what does this give evidence for ?

A

the deviations can be explained by the existence of energy levels, sublevels and orbitals

35
Q

how to compare IEs

A

make sure know the e- configuration for whatever is brings asked, atom or ion

who has a smaller atomic radius?
who has more shielding?
which orbital is outer e-?
who has higher nuclear charge?
which main energy level?

36
Q

what is TOF mass spectrometry

A

? Girl beats me

37
Q

what’s the abbreviated process

A

VIA DD

vaporisation
ionisation
acceleration
drift
detection

38
Q

in vaporisation…

A

substance is made into a gas bc . needs to

39
Q

in ionisation…

A

the particles are made to have +ve charges because that is the only way they can be accelerated and detected.

they can have this done in two ways:

electron impact
or electrospray

40
Q

electron impact

A

high energy electrons are fired from an electron gun at the sample. knocks off an electron and results in a +1 charge

this is usually done for

41
Q

electrospray

A

dissolve sample in polar volatile solvent;
inject through a fine hypodermic needle to give a fine mist;
top of needle has a high voltage;
gains a proton as it leaves the needle

charged sample moves toward -ve plate and repel as they get closer so a stream of charged particles is produced

42
Q

in acceleration…

A

ions are accelerates using an electric field so ions all have the same kinetic energy. they are headed towards a -vely charged plate.

heavier ions will have slower velocity, therefore hit the detector plate later. so different mass ions have different times of flight

43
Q

in drift…

A

ions passing through the flight tube (vacuum so doesn’t hit air particles) towards detector.

time of flight determines the mass of the ion (have the KE, the distance and now the time)

44
Q

equation for determining mass of ion with tof ms

A

t= d√(m/2ke)

time, s
distance (of flight tube), m
mass, kg
ke, J

45
Q

in detection…

A

electron transfers from the detector to the +be ion when the ion hits it. this induced a current. the size of this current tells us the abundance of that ion because they will all hit at same time (same mass so same tof)

how many different currents you get (or at different times idk?) tells you the number of isotopes. the size for the current is proportional to abundance of that isotope.

46
Q

if electrospray is used, when reading a m/z graph we need to

A

take away 1 from mass reading because a proton has been added

47
Q

reasonably sized peaks on an m/z graph indicate

A

an isotope

48
Q

m/z graphs shows the

A

relative abundance (obtained from current) of different isotopes of an element sample

49
Q

m+1 peaks

A

for molecules, small peaks to the right of the main peak showing molecular mass are due to there being different isotopes of elements used in the molecules eg C13 instead of C12 and H2 instead of H1

50
Q

the Mr of a compound from a graph

A

the leak with the greatest (!) m/z value ignoring m+1 peaks. this is the molecular ion peak