Atomic Struc Flashcards

1
Q

Defn of atom

A

Atom is the smallest particle found in an element that can take part in a chemical rctn

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2
Q

Subatomic particle - location, relative mass, relative charge, symbol

A

E- in orbitals around nucleus, 1/1840 , -1, (0 -1) e
Neutron - nucleus, 1, 0, (1 0) n
Proton -nuclues, 1, +1, (1 1) p

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3
Q

Behaviour of subatomic particles in an electric field (3)

A
  1. Same speed
  2. diff direction of deflection
  3. diff angle of deflection
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4
Q

how to find angle of deflection and stuff (formula)

A

angle of deflection prop. to | q/m | when solving qn use the constant k

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5
Q

what is a nuclide

A

any species of given mass no. and atomic no. (eg hydrogen - 1) - elemental name & mass no

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6
Q

What is nucleon no.

A

mass no

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7
Q

what is mass no.

A

nucleon no.

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8
Q

What is atomic no.

A

proton no.

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9
Q

sig of atomic no.

A

determines the identity of an atom

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10
Q

isotopes & their properties

A

same no. of protons/e- but diff neutrons - same chem properties n diff/masses/phy properties

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11
Q
How to solve
(235 92) U + (1 0) n -> Y + (90 36) Kr + 2 (1 0) n 
nucleon no. of Y = 
Proton no. of Y = 
Hence Y is =
A

Nucleon no. of Y = 235+1-90-2 = 144
Proton no. of Y = 92-36 = 56
Hence Y = (144 56) Ba

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12
Q

Principle quantum shell, All the subshells, no. of orbitals, types of orbitals - name, shape, direction, size

A

Subshells: s, p, d, f
S: 1 - spherical shape, non directional
P: 3 -dumbbell shape, directional as the e- density is concentrated in certain directed along…axes
D: 5 -
d xz & d xy & d yz - 3 orbitals with similar 4-loped shape, orbitals have their lobes pointing b/w the axes
d x^2 - y^2 - 4 lobed shape, lobes aligned along the x & y axes
d z^2 - dumbbell shaped surrounded by a small doughnut shaped ring at its waist, orbital is aligned along the z axis

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13
Q

the greater the value of n … (4)

A

further the shell is from the nucleus, higher the energy lvl of the shell
higher the energy lvl of the shell/e-
weaker the electrostatic attraction b/w nuceus and e-
larger size of orbital

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14
Q

energy lvl diagram & the exception

A

4s<3d

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15
Q

3 basic rules to write e- configuration

A

Aufbau principle - e- fill orbitals from the lowest energy orbital upwards
Hund’s rule - orbitals of a subshell must be occupied singly by an e- of parallel spins before pairing can occur
Pauli exclusion principle - each orbital can hold a max of 2 e- and they must be of opp. spins

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16
Q

why are paired e- stable

A

when they spin in opp directions, the magnetic attraction which results from their opp spins can counterbalance the electrical repulsion which results from their identical charges

17
Q

2 anomalous e- configuration and why are they more stable ( general reason and indiv reason)

A

Cr & Cu - a ‘d’ subshell that is half-fulled or full is more stable -
for Cr: as 3d & 4s are abt equal in energy by the time Cr is reached, so by having 1 e- each in the 4d and 4s orbitals, inter-electronic repulsion is minimized
For Cu: the fully filled 3d subshell is unusually stable due to the symmetrical charge distribution around the metal center

18
Q

excited state

A

one or more e- absorb energy and are promoted to a higher energy lvl

19
Q

are 4s e- lost before or after 3d e-? and why

A

once e- occupy the inner 3d orbitals, they provide some shielding for the outermost 4s e- hence they repel the 4s e- to a slightly higher energy lvl

20
Q

isoelectronic species

A

species with the same total no. of e-

21
Q

e- configuration from the periodic table

A

s- block - ns^1 ns&2
d-block - (n-1)d1 ns^y - the 1 is starting from the first transition metal
p-block - ns^2np^1 -> ns^2np^6

22
Q

Defn of atomic radius

A

Half the shortest inter-nuclear dist found in the struc of the element

23
Q

Variation in atomic radii across period

A

DECREASE as
No.of e- shells remain the same
no. of protons, hence nuclear charge increases
e- increase but since they are added to the valence shell, the shielding effect remains approx const
effective nuclear charge increases
electrostatic attraction b/w nucleus and valence e- increases
decrease in size of e- cloud

24
Q

Variation in atomic radii down grp

A

INCREASE
although protons increase, nuclear charge increases
no. of e- shell increases, dist b/w nucleus and valence e- increase
hence, the electrostatic attraction b/w the nucleus and the valence e- decreased
increase in size of e- cloud

25
Q

Cationic radius vs atom

A

rcation

26
Q

Anionic radius vs atom

A

ratom

27
Q

Ionic radii of isoelectronic species across period

A

DECREASE
Na+, Mg2+, Al3+ are all isoe- species and hecne their valence e- exp the same shielding effect
nuclear charge increases from Na+ to Al3+
effective nuclear charge increases from Na+ to Al3+
electrostatic attraction b/w the nucleus and valence e- increase resulting in decreases in size of e- cloud

28
Q

Why would there be a sharp increase in ionic radius from Al3+ to P3-

A

P3- has 1 more e- shell than Al3+
Despite the increase in nuclear charge, the valence e- of P3- are less strongly attracted by the nucleus
Ionic radius of P3- is bigger than that of Al3+

29
Q

Trend of 1st ionisation energies across the period

A

INCREASE
no. of e- shell remain the same
no. of protons increase, nuclear charge increase
no. of e- increase, but they are added to the valence shell so shielding effect remains approx const
effective nuclear charge increases
electrostatic attraction b/w nucleus and valence e- increase
increase in energy required to remove the valence e- from an atom

30
Q

Irregularity in ionisation energies across a period (2)

A

Grp 2 & 13 ———— grp 13<2
Al vs Mg:
3p e- to be removed from Al is at a higher energy lvl than the 3s e- to be removed from Mg
Hence less energy is required to remove the 3p e- in Al than the 3s e- in Mg

Grp 15 & 16 ————- grp 16<15
S vs P:
The 3p e- to be removed from S is a paired e- while that to be removed from P is an unpaired e-
Due to inter-electronic repulsion b/w paired e- in the same orbital, less energy is required to remove the paired 3p e- from S

31
Q

Trend of 1st e- energies down a grp

A

DECREASE
no. of e- shells increase
dist b/w nucleus and valence e- increase
despite increase in nuclear charge,
electrostatic attraction b/w the nucleus and the valence e- deceases,
resulting in a decrease in the energy required to remove the valance e- from an atom

32
Q

Trend in successive ionisation energies of an element

A

INCREASE
once the 1st e- is removed from the neutral atom, each successive e- is removed from an ion of increasing +ve charge which attracts the e- more strongly, hence more energy is required for the removal of the e-

33
Q

How to deduce grp no. from successive ionisation data

A

A large jump in the 5th and 6th IE is observed
Sig more energy is required to remove the 6th e- as it is located in an inner electronic shell that is nearer to the nucleus and is hence more strongly attracted by the nucleus.
5e- in the valence shell
E is likely to be in grp 15

34
Q

Defn of electronegativity

A

Relative measure of its ability to attract bonding e-

35
Q

Trend in electronegativity across period

A

INCREASE
no. of e- shell remain the same
no. of protons increase, nuclear charge increase
no. of e- increase, but they are added to the valence shell so shielding effect remains approx const
effective nuclear charge increases
electrostatic attraction b/w nucleus and valence e- increase

36
Q

Trend in electronegativity down grp

A

DECREASES
no. of shells increase
dist b/w the nucleus and the bonding e- increase
despite increase in nuclear charge, electrostatic attraction b/w the nucleus and the bonding e- decreases

37
Q

Why is the 3rd IE of mg much higher than that of aluminium

A

Al2+ has one more e- shell than Mg2+, the 3s e- in Al2+ is further from the nucleus, has higher energy and shielded by more inner e- shells than the 2p e-
Hence the 3s e- in Al2+ is less strongly attracted by the nucleus and requires less energy to be removed compared to the 2p e- in Mg2+