Coordinate Compounds Flashcards

1
Q

Coordinate compounds

A

Those compounds in which metal atoms or ions are bonded to ions or neutral molecules by coordinate bond

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2
Q

The product written in [] is called __ and outside is __

A

Complex part; counter ion

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3
Q

Product when Cuso4 + nh3

A

[Cu(NH3)⁴]SO⁴

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4
Q

Product of NiCl² + 4nh3

A

[Ni(nh3)⁴]Cl

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5
Q

Ligands are

A

Charged ions or neutral molecules that can give 2 e’s to form coordinate bond

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6
Q

How many ions will form when h20 + [Co(nh3)⁴Cl²]Cl?

A

2, i.e [Co(nh3)⁴Cl²] & Cl

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7
Q

Which will ionise in solution, Double salt or coordinate compds?

A

Double salt

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8
Q

Monodentate/unidentate ligands

A

Ligands which are able to form only 1 coordinate hond

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9
Q

Examples of monodentrate

A

NH³,H2O,PH³,P(C⁶H⁵)³,CH³-NH²
charged ligands like hallides, OH, NO², NO³

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10
Q

Ambidentate ligands

A

Ligands that can form bonds in 2 ways by 2 atoms

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11
Q

Ambidentate ligands examples

A

A metal with NO², SCN

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12
Q

Bidentate ligands

A

Ligands which can form only 2 bonds

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13
Q

Ex of bidentate

A

NH²–CH²-CH²–NH² where N has 1 lone pair, oxalic acid,glycine

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14
Q

Coordination compounds of Mg, Fe & Co

A

Chlorophyll,haemoglobin & Vitamin B¹²

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15
Q

Applications of coordination compounds

A

Electroplating, textile dyeing & medicinal chemistry

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16
Q

Ex of double salts

A

Carnallite,KCl.MgCl2.6H2O,Mohr’s salt,potash alum

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17
Q

Central atoms are also called

A

Lewis acids

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18
Q

Number of ligating groups are called

A

Denticity of the ligand

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19
Q

Oxalic acid structure

A

HooC-CooH

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20
Q

Among amino acids, which one is optically inactive

A

Glycine ²HN-CH²-COOH since it is not chiral

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21
Q

Ex of hexadentate ligands

A

Ethylene diamine tetraacetate ion(EDTA⁴-), [Co(en)³]³+

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22
Q

Among [Co(Nh3)⁶]³+ and [Co(en)³]³+ which is more stable?

A

[Co(en)³]³+ since it forms a ring structure

23
Q

Chelate ligand

A

Di- or polydentate ligand that uses its 2 or more atoms to bind

24
Q

Which complex is more stable? Chelate or unidendate?

25
Coordination polyhedral
Shape of the complex decided by no of bonds formed
26
Coordination number
The no of coordination bonds the ligands are forming with metal
27
Homoleptic vs heterolyptic complex
All ligands are same; different
28
Cation complex
Complexes with only +vely charged part
29
OH- name
Hydroxo
30
NO² name
Nitrito-N or nitrito-O
31
SO⁴ name
Sulphato
32
(CO³)²- name
Carbonato
33
Nh3 name
Ammine
34
H20 & CO name
Aqua; carbonyl
35
NO name
Nitrocyl
36
(C2O8)²- name
Oxalato
37
Werner's theory
A metal ion has a primary & secondary valence where primary is satisfied by ions & secondary by ligands
38
Postulates of werner's theory
Metals show 2 linkages-primary & sec Primary are satisfied by -ve ions and are ionisable Secondary are non-ionisable & satisfied by neutral molecules Ions bound by sec have spatial arrangements
39
Elements from 20 to 30
Sc,Ti,Vi,Cr,Mn,Fe,Co,Ni,Cu,Zn
40
Valence bond theory
Metal atoms or ion under the influence of ligands can use its orbitals for hybridization to yield a set of equivalent orbitals of definite geometry
41
Why is [Co(nh3)⁶]³+ diamagnetic?
Absence of unpaired electrons
42
Spin magnetic moment
No of unpaired electrons Myu = [(n+2)n]½ BM
43
Myu is 0 for
Diamagnetic substances
44
2 exceptions btw 20 and 30 Atomic nos
Cromium and Copper
45
If a substance has d²sp³ it is
An inner orbital complex
46
How to identify strong and weak ligands
C>N>O>X
47
Hybridisation & shape of 4 ligands
sp³ - tetrahedral dsp² - square planar
48
Hybridisation & shape of 5 ligands
dsp³ & sp³d - trigonal bipyramidal
49
Hybridisation & shape of 6 ligands
sp³d² or d²sp³ - octahedral
50
Total magnetic moment
Orbital MM + spin MM
51
Drawbacks of VBT
Doesn't tell why some subs are inner orbital and outer orbritsl complexes Doesn't differentiate b/n strong & weak ligands In some, actual MM & calculated MM are not same Couldn't explain why [Cu(NH3)⁴]²+ is square planar & not tetrahedral Couldn't explain why some NI(||) complexes are paramagnetic
52
Crystal field theory
When a metal atoms or ion is surrounded by -vely charged ligands, electrostatic forces exist b/n them (ionic bond). Ligands are point -ve charges. Degeneration of metal orbitals are lost due to repulsion b/n orbitals. D-orbitals will be split according to the geometry of the complex
53
Among d(xy), d(yz), d(xz), d(x²-y²) & d(z²), which has more energy?
d(x²-y²) & d(z²)
54
Energy difference caused due to splitting is
Crystal field splitting theory Denoted by delta°