unit 1a: transition metals Flashcards

(74 cards)

1
Q

transition metals

A

metals with an incomplete d-subshell in at least one of their ions

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2
Q

variable valency

A

transition metals can form ions with different charges by losing different numbers of electrons

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3
Q

scandium and zinc

A

these are not transition metals as there is not an incomplete d-subshell in the ions they form

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4
Q

properties

A

form coloured ions, form complexes, variable oxidation states, show catalytic activity

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5
Q

oxidation state

A

an element is said to be in a particular oxidation state when it has a specific oxidation number, related to the number of electrons the species has lost or gained

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6
Q

oxidation number in a free element

A

0 e.g. Mg=0 and Cl2=0

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7
Q

for monatomic ions, the oxidation number is

A

equal to the charge, e.g. Cl^-1=-1 and Al^3+=+3

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8
Q

oxidation number for oxygen

A

-2

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9
Q

oxidation number for hydrogen

A

+1

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10
Q

group 1 metals and group 2 metals

A

+1 and +2

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11
Q

oxidation number in compounds

A

fluorine, the CN^-1 ion, and all of group 7 is always equal to -1

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12
Q

in molecule the sum of all oxidation numbers is

A

equal to 0, e.g. H20=0

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13
Q

in a polyatomic ion, the sum of the oxidation numbers is

A

equal to the charge of the ion, e.g. SO4^2-=-2

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14
Q

oxidation involves

A

increase in oxidation number

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15
Q

reduction involves

A

decrease in oxidation number

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16
Q

metals high in oxidation states tend to be good

A

oxidising agents

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17
Q

what two elements in the box are not transition metals

A

scandium and zinc

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18
Q

redox acronym

A

OILRIG

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19
Q

ligand definition

A

electron donors, may be negative ions or molecules with non-bonding pairs of electrons

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20
Q

a complex consists of

A

a central metal ion surrounded by ligands

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21
Q

dative bond

A

when both electrons of the shared pair come from the same atom

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22
Q

ligands have at least

A

one lone pair of electrons

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23
Q

monodentate

A

when a ligand uses just one atom to bind to the central metal

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24
Q

bidentate

A

when a ligand uses two atoms to bind to the central metal

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25
example of a hexadentate ligand
ethylenediaminetetraacetate- EDTA
26
monodentate ligands- negative ions
fluoride F- , chloride Cl- , cyanide CN-
27
monodentate ligands- neutral molecules
water H2O , ammonia NH3
28
bidentate ligand- negative ion
oxalate C2O4^2-
29
coordination number
the total number of bonds from the ligands to the central transition metal atom/ion
30
if the complex ion is negative the transition metal name will end in
-ate
31
if the ligand is a negative ion the name in complex will
replace the “e” ending with “o” e.g. bromine —> bromido
32
CO name in complex ion
carbonyl
33
H2O name in complex ion
aqua
34
NH3 name in complex ion
ammine
35
Fe name in complex ion
ferrate
36
Cu name in complex ion
cuprate
37
coordination compound
when a complex ion combines with oppositely charged ions
38
if the complex is a positive ion it will appear
first in the formula and the name
39
if the complex is a negative ion
it will appear last in the formula and the name
40
three primary colours of visible light
red , green , and blue
41
complementary colour
transmitted light from certain chemicals(when white light shines on certain chemicals they may absorb some of the. visible light, the colour we see is the white light minus absorbed light)
42
when red light is absorbed
blue and green are transmitted and cyan is observed
43
when blue light is absorbed
red and green are transmitted and yellow is observed
44
when green light is absorbed
red and blue are transmitted and magenta is observed
45
a more concentrated soloution will absorb more
light than a dilute solution and be darker in colour
46
extent of d orbital splitting factors
the metal involved , the oxidation state of the metal , the nature of the ligand
47
spectra chemical series
CN-, NH3, H2O, OH-, F-, Cl-, Br-, I-
48
start of the spectrochemical series
weaker field , smaller delta , longer wavelength
49
end of the spectrochemical series
stronger field , larger delta , shorter wavelength
50
weakest at splitting d orbitals
I-
51
strongest at splitting d orbitals
CO
52
crystal field theory
explains how transition metals (with an incomplete 3d subshell) are coloured, only applies to octahedral complexes
53
splitting
as a result of ligands approaching and bonding to the metal, the five 3d orbitals are no longer degenerate
54
delta
the splitting energy
55
d to d transition
when any of the three lower d orbitals absorb energy and are promoted to one of the two higher energy d orbitals
56
how the metals transmit the colours
if the energy absorbed is equal to a wavelength of light in the visible spectrum, the compound will transmit its complementary colour
57
catalyst of the haber process
iron
58
catalyst of the contact process
vanadium (V) oxide
59
catalyst of the ostwald process
platinum
60
catalyst for catalytic converters in cars
platinum , palladium , rhodoum
61
catalyst for the production of methanol
copper
62
catalyst for the hardening of oils to fats
nickel
63
catalyst for the polymerisation of alkenes
titanium compounds
64
how catalysts speed up chemical reactions
by providing an alternative reaction pathway of lower activation energy
65
why do many transition metals act as catalysts
due to their ability to exist in a variety of different oxidation states
66
how do ligands form complexes with metal atoms
donate pairs of electrons
67
homogeneous
same state as reactants, change their oxidation allowing formation of intermediate complexes, then reverts back to its original state
68
heterogeneous
different state as reactants, work by absorption of the reactant molecules to their active sites, presence of unpaired d-electron allow activated complex to form providing an alternative pathway and activation energy
69
how do transition metals act as catalysts
unpaired d electrons (donating and accepting electrons)
70
how do unpaired electrons arise in H20 easier than in CN-
H2O has a smaller splitting energy so it is easier for electrons to jump up to the higher energy d orbitals
71
why are transition metals coloured
light is absorbed when electrons in lower energy d orbitals are promoted in a d-d transition, if the energy absorbed is visible light then it will be coloured
72
changing the ligand in a complex can
change the colour
73
a complex may be colourless because
it was in the UV spectrum, it has a full d subshell
74
what causes d orbital splitting
lone pairs of electrons in the ligand