periodicity– transition metals Flashcards

1
Q

what are transition metals? (short defin.)

A
  • a d-block element that forms 1 or more stable ions w partially filled d subshell
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2
Q

what are the exceptions in the transition metals?

A

Zn, Sc3+, Cu+

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3
Q

why is Zn not considered a transition metal?

A
  • it forms only 1 ion, Zn2+
  • Zn2+ has a fully filled d subshell
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4
Q

why is Sc3+ not considered a transition metal?

A

it has no e- in its d subshell

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5
Q

why is Cu+ not a transition metal?

A

it has a fully filed d subshell

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6
Q

____ orbitals are filled before ___

A

4s, 3d

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7
Q

in transition metals, 4s is filled before 3d except for…

A

Cr and Cu

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8
Q

why do Cr and Cu not have a fully filled 4s orbital?

A
  • Cr -> 3d orbitals are half filled and more stable than fully filled 4s
  • Cu -> 3d orbitals are fully filled and stable
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9
Q

d-block metals have a [higher/lower] m.p. compared to s-block metals

A

higher

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10
Q

is the atomic radii of transition metals generally larger or smaller than s-block metals?

A

smaller

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11
Q

transition metals are [more/less] dense than s-block metals

A

more

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12
Q

_____ metals are poorer conductors of electricity compared to ______ metals

A

s-block, d-block

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13
Q

why is the atomic and ionic radii of d-block elements smaller than s-block elements?

A
  • d subshell SE not as effective as p subshell
    • as d subshells are more diffused
  • valence shell for d-block elements exp greater nuclear attraction -> smaller radii
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14
Q

how does the atomic radius change across the period and why?

A
  • decr slightly:
    • due to nuclear charge incr slightly -> SE incr slightly -> ENC increases slightly
    • thus radius decr slightly
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15
Q

what is the trend for ionisation energies across the period?

A
  • incr slightly
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16
Q

why does ionisation energies incr slightly from s-block to d-block

A
  • p subshell provides better shielding than d subshell
    • d subshells more diffused
  • valence shell of d-block elements exp greater nuclear attraction
  • thus greater IE for d-block
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17
Q

there is a ______ incr from 1st to 2nd IE, and a _______ incr from 2nd to 3rd IE

A

small, large

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18
Q

there is a small incr from 1st to 2nd IE because…

A

both first and second electrons are removed from the same orbital, 4s

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19
Q

the large increase from 2nd to 3rd IE in d block elements is because…

A
  • third electron is removed from 3d subshells
  • SE decr -> ENC incr
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20
Q

why is the 2nd IE of Mn lower than that of Cr?

A
  • 2nd e- removed from Mn is 4s
  • 2nd e- removed from Cr is 3d
  • 4s is in outer shell -> experiences weaker ENC
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21
Q

why is the 3rd IE of Mn>Fe?

A
  • Fe = 3d6
  • electron removed is in the same orbital as another electron
    • inter-electronic repulsion
  • thus less energy req
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22
Q

why do trans elements have greater m.p. than s-block?

A
  • 3d + 4s energies are relatively similar
    • TM can lose more valence e-
    • thus more delocalised e-
  • stronger electrostatic FOA btw metal cation and sea of delocalised e-
  • TMS have stronger metallic bonding -> higher m.p.
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23
Q

what is the trend of m.p. across the d-block?

A

incr then decr

24
Q

why does m.p. increase from Sc to Cr?

A
  • Cr has 5 unpaired e- (3d)
  • Sc has 1 unpaired e- (3d)
  • Cr has more unpaired e- in 3d subshell
  • thus stronger metallic bonding
25
why does m.p. decrease from Fe to Zn?
- less unpaired e- in 3d subshell - weaker metallic bonding
26
why are d-block elements more dense than s-block
- stronger metallic bond strength - smaller atomic radii thus more closely packed
27
why does Mn have a lower m.p.?
Cr: 4s1 3d5 Mn: 4s2 3d5 - Mr has less unpaired e- - thus weaker metallic bonds - lower m.p.
28
the density of d-block elements ______ across the period as...
incr - atomic radii decr slightly - more atoms can be packed closely together
29
what are the two forms of magnetism?
paramagnetism, diamagnetism
30
paramagnetism is when..
an ion, molecule, atom has unpaired e-
31
paramagnetic substances are [attracted/repelled] by a magnetic field, as...
attracted - unpaired e- give rise to a magnetic field that can be affected by external magnetic field
32
diamagnetism is caused by ______ e-.
paired
33
how do diamagnetic substances respond to a magnetic field?
they are repelled
34
how do you find the maximum oxidation state of a TM?
no. 4s e- + no. 4d e-
35
what is a catalyst?
a substance that **incr the ROR** by **providing an alternative rxn pathway** that **lowers Ea**
36
what are the two types of catalysts?
- homogenous - heterogenous
37
heterogenous catalysts are in a ______ ________ as the reactants
diff phase
38
how do TMs act as heterogenous catalysts? (3)
1. reactants adsorb to e active sites of catalyst - weakens the covalent bonds within the rxt molecules - lowers Ea for the rxn 2. it incr surface conc and ensures proper orientation for the rxn 3. products deabsorb fr e active site -> freeing up active sites
39
why can TMs act as homogenous catalysts? (1)
- they can form variable oxidation states - i.e. they can be easily converted fr one ox state to another
40
what are ligands? (defin.)
an anion or molecule that has at least one lone pair of e- that can be donated into the vacant orbitals in the central metal atom
41
what are complexes? (defin.)
a complex consists of a **central metal atom or ion** surrounded by other ions or molecules called **ligands** through **dative bonds**
42
ligands act as _______
Lewis bases
43
why can TMs form complexes? (2)
their metal cations have 1. high charge densities - hence high polarising power -> cations can attract lone pair of e- from ligands 2. vacant, low-lying 3d orbitals - can accept lone pair of e- donated by ligands -> dative bond formed
44
ligands can be _________ charged or ___________ charged
neutrally or negatively
45
why are ligands Lewis bases?
they are e- pair donors
46
a ligand that forms 2 dative bonds is called...
bidentate
47
what is ligand exchange?
a stronger ligand replacing a weaker ligand from a cation complex
48
ligand exchange can be seen through observing a _______________
colour change
49
why are TM complexes coloured? (short)
due to the presence of partially filled d-orbitals
50
why are some TM complexes colourless?
- complexes with Sc3+ ion -> 3d subshell is empty - Zn2+ -> 3d subshell is full
51
why do transition metals form coloured compounds? (4)
- in the presence of ligands, the d orbital splits into 2 energy levels - an e- in the lower energy level is able to be promoted to the higher energy level - by absorbing a wavelength of light in the visible region - the complimentary colour of the light absorbed is observed
52
what affects the colour of complexes? (2)
1. nature and oxidation state of TM 2. nature of ligands
53
how does the nature and oxidation state of TM affect the colour of complexes?
- diff no. of e- in the d orbitals repel e- of ligands to a diff extent - gives rise to diff energy gaps -> diff colour
54
the nature of ligands affects the colours of complexes as...
diff ligands split the d-orbitals to a diff extent
55
the longest wavelength is...
red
56
what is the shortest wavelength?
violet