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Chemistry · Class 12 Science

Ch 5Coordination Compounds — Class 12 Chemistry, concept-first.

The previous unit on the d- and f-block elements established that transition metals readily form a large number of complex compounds, in which a metal atom or ion is bound to a set of surrounding anions or neutral molecules through shared electron pairs.

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Key concepts

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Chapter contents

The NCERT structure, section by section. Open a section to see its questions, then read the concept-first solution.

Introduction

The previous unit on the d- and f-block elements established that transition metals readily form a large number of complex compounds, in which a metal atom or ion is bound to a set of surrounding anio…

5.1

Werner's Theory of Coordination Compounds

Transition metals readily bind to a number of anions or neutral molecules through shared electron pairs, producing what are now called coordination compounds.

5.2

Definitions of Some Important Terms Pertaining to Coordination Compounds

At the heart of coordination chemistry is the coordination entity: a central metal atom or ion held together with a fixed set of surrounding ions or molecules.

5.3

Nomenclature of Coordination Compounds

A coordination compound can often be built up from a metal and a chosen set of ligands in more than one arrangement, and different arrangements — the isomers you will meet in the next section — can be…

5.3.1

Formulas of Mononuclear Coordination Entities

A formula is a compact way of stating what a compound is made of. For a mononuclear coordination entity — one built around a single central metal atom or ion — the formula is assembled by following a…

5.3.2

Naming of Mononuclear Coordination Compounds

4 Q

Naming a coordination compound follows the principles of additive nomenclature: every group attached to the central atom is identified individually and then listed, as a prefix, in front of the name o…

5.4

Isomerism in Coordination Compounds

Isomers are two or more compounds that share the same chemical formula but differ in how their atoms are arranged in space.

5.4.1

Geometric Isomerism

Geometric (geometrical) isomerism arises in heteroleptic complexes — complexes bonded to more than one kind of ligand — because of the different geometric arrangements the ligands can adopt around the…

5.4.2

Optical Isomerism

Optical isomers are mirror images of one another that cannot be superimposed on one another, no matter how they are rotated in space.

5.4.3

Linkage Isomerism

Linkage isomerism arises in a coordination compound that contains an ambidentate ligand — a ligand which possesses more than one kind of donor atom, so that it can attach itself to the central metal t…

5.4.4

Coordination Isomerism

Coordination isomerism arises in a compound that is built from both a cationic coordination entity and an anionic coordination entity, each centred on a different metal.

5.4.5

Ionisation Isomerism

Ionisation isomerism arises when the counter ion of a complex salt — the ion lying outside the coordination sphere — is itself capable of acting as a ligand.

5.4.6

Solvate Isomerism

Solvate isomerism is closely related to ionisation isomerism, and takes the specific name hydrate isomerism in the particular case where the solvent involved is water.

5.5

Bonding in Coordination Compounds

Werner had already described what a coordination compound looks like — a central metal surrounded by a fixed number of ligands in a definite geometry — but his theory was silent on why this happens.

5.5.1

Valence Bond Theory

Valence Bond Theory pictures the formation of a coordination entity as a hybridisation event on the metal atom or ion.

5.5.2

Magnetic Properties of Coordination Compounds

The magnetic moment of a coordination compound can be measured experimentally through magnetic susceptibility measurements.

5.5.3

Limitations of Valence Bond Theory

Valence Bond Theory does a reasonably good job of accounting for the formation, geometry, and magnetic behaviour of many coordination compounds.

5.5.4

Crystal Field Theory

Crystal Field Theory (CFT) takes a completely different starting point from VBT. It treats the metal–ligand bond as purely electrostatic (ionic), arising from the attraction and repulsion between the…

5.5.5

Colour in Coordination Compounds

One of the most striking features of transition metal complexes is the sheer range of colours they display.

5.5.6

Limitations of Crystal Field Theory

Crystal Field Theory is, to a large extent, genuinely successful — it gives a workable account of the formation, structures, colour, and magnetic properties of coordination compounds, and it does all…

5.6

Bonding in Metal Carbonyls

A metal carbonyl is a coordination compound in which the ligand is carbon monoxide. When every ligand attached to the metal is CO, the compound is called homoleptic.

5.7

Importance and Applications of Coordination Compounds

Coordination compounds are not just a theoretical curiosity — they occur naturally across the mineral, plant and animal worlds, and they are put to deliberate use across analytical chemistry, metallur…

Summary

- Coordination entity: A central metal ion/atom bonded to a fixed number of ligands (ions/molecules) via coordinate bonds. Example: .

Exercises

+Show 31 questions31 questions
  1. 5.1Explain the bonding in coordination compounds in terms of Werner's postulates.Free
  2. 5.2$FeSO_4$ solution mixed with $(NH_4)_2SO_4$ solution in 1:1 molar ratio gives the test of $Fe^{2+}$ ion but $CuSO_4$ solution mixed with aqu…Free
  3. 5.3Explain with two examples each of the following: coordination entity, ligand, coordination number, coordination polyhedron, homoleptic and h…Free
  4. 5.4What is meant by unidentate, didentate and ambidentate ligands? Give two examples for each.Preview
  5. 5.5Specify the oxidation numbers of the metals in the following coordination entities: (i) $[Co(H_2O)(CN)(en)_2]^{2+}$ (ii) $[CoBr_2(en)_2]^{+}…Preview
  6. 5.6Using IUPAC norms write the formulas for the following: (i) Tetrahydroxidozincate(II) (ii) Potassium tetrachloridopalladate(II) (iii) Diammi…Preview
  7. 5.7Using IUPAC norms write the systematic names of the following: (i) $[Co(NH_3)_6]Cl_3$ (ii) $[Pt(NH_3)_2Cl(NH_2CH_3)]Cl$ (iii) $[Ti(H_2O)_6]^…Preview
  8. 5.8List various types of isomerism possible for coordination compounds, giving an example of each.Preview
  9. 5.9How many geometrical isomers are possible in the following coordination entities? (i) $[Cr(C_2O_4)_3]^{3-}$ (ii) $[Co(NH_3)_3Cl_3]$Preview
  10. 5.10Draw the structures of optical isomers of: (i) $[Cr(C_2O_4)_3]^{3-}$ (ii) $[PtCl_2(en)_2]^{2+}$ (iii) $[Cr(NH_3)_2Cl_2(en)]^{+}$Preview
  11. 5.11Draw all the isomers (geometrical and optical) of: (i) $[CoCl_2(en)_2]^{+}$ (ii) $[Co(NH_3)Cl(en)_2]^{2+}$ (iii) $[Co(NH_3)_2Cl_2(en)]^{+}$Preview
  12. 5.12Write all the geometrical isomers of $[Pt(NH_3)(Br)(Cl)(py)]$ and how many of these will exhibit optical isomers?Preview
  13. 5.13Aqueous copper sulphate solution (blue in colour) gives: (i) a green precipitate with aqueous potassium fluoride and (ii) a bright green sol…Preview
  14. 5.14What is the coordination entity formed when excess of aqueous $KCN$ is added to an aqueous solution of copper sulphate? Why is it that no pr…Preview
  15. 5.15Discuss the nature of bonding in the following coordination entities on the basis of valence bond theory: (i) $[Fe(CN)_6]^{4-}$ (ii) $[FeF_6…Preview
  16. 5.16Draw figure to show the splitting of d orbitals in an octahedral crystal field.Preview
  17. 5.17What is spectrochemical series? Explain the difference between a weak field ligand and a strong field ligand.Preview
  18. 5.18What is crystal field splitting energy? How does the magnitude of $\Delta_o$ decide the actual configuration of d orbitals in a coordination…Preview
  19. 5.19$[Cr(NH_3)_6]^{3+}$ is paramagnetic while $[Ni(CN)_4]^{2-}$ is diamagnetic. Explain why?Preview
  20. 5.20A solution of $[Ni(H_2O)_6]^{2+}$ is green but a solution of $[Ni(CN)_4]^{2-}$ is colourless. Explain.Preview
  21. 5.21$[Fe(CN)_6]^{4-}$ and $[Fe(H_2O)_6]^{2+}$ are of different colours in dilute solutions. Why?Preview
  22. 5.22Discuss the nature of bonding in metal carbonyls.Preview
  23. 5.23Give the oxidation state, d orbital occupation and coordination number of the central metal ion in the following complexes: (i) $K_3[Co(C_2O…Preview
  24. 5.24Write down the IUPAC name for each of the following complexes and indicate the oxidation state, electronic configuration and coordination nu…Preview
  25. 5.25Explain the violet colour of the complex $[Ti(H_2O)_6]^{3+}$ on the basis of crystal field theory.Preview
  26. 5.26What is meant by the chelate effect? Give an example.Preview
  27. 5.27Discuss briefly giving an example in each case the role of coordination compounds in: (i) biological systems (ii) medicinal chemistry and (i…Preview
  28. 5.28How many ions are produced from the complex $Co(NH_3)_6Cl_2$ in solution? (i) 6 (ii) 4 (iii) 3 (iv) 2Preview
  29. 5.29Amongst the following ions which one has the highest magnetic moment value? (i) $[Cr(H_2O)_6]^{3+}$ (ii) $[Fe(H_2O)_6]^{2+}$ (iii) $[Zn(H_2O…Preview
  30. 5.30Amongst the following, the most stable complex is (i) $[Fe(H_2O)_6]^{3+}$ (ii) $[Fe(NH_3)_6]^{3+}$ (iii) $[Fe(C_2O_4)_3]^{3-}$ (iv) $[FeCl_6…Preview
  31. 5.31What will be the correct order for the wavelengths of absorption in the visible region for the following: $[Ni(NO_2)_6]^{4-}$, $[Ni(NH_3)_6]…Preview

Answers to Intext Questions

These are the final answers printed at the end of the NCERT chapter. The book gives answers for some intext questions only — every question below links to our complete worked solution.

Exemplar Problems

Higher-order thinking / exemplar-style practice problems.

+Show 50 questions50 questions
  1. Q1Which of the following complexes formed by $Cu^{2+}$ ions is most stable? (i) $Cu^{2+} + 4NH_3 \rightleftharpoons [Cu(NH_3)_4]^{2+}$, $\log…Free
  2. Q2The colour of the coordination compounds depends on the crystal field splitting. What will be the correct order of absorption of wavelength…Free
  3. Q3When 0.1 mol $CoCl_3(NH_3)_5$ is treated with excess of $AgNO_3$, 0.2 mol of $AgCl$ are obtained. The conductivity of solution will correspo…Free
  4. Q4When 1 mol $CrCl_3 \cdot 6H_2O$ is treated with excess of $AgNO_3$, 3 mol of $AgCl$ are obtained. The formula of the complex is: (i) $[CrCl_…Preview
  5. Q5The correct IUPAC name of $[Pt(NH_3)_2Cl_2]$ is (i) Diamminedichloridoplatinum (II) (ii) Diamminedichloridoplatinum (IV) (iii) Diamminedichl…Preview
  6. Q6The stabilisation of coordination compounds due to chelation is called the chelate effect. Which of the following is the most stable complex…Preview
  7. Q7Indicate the complex ion which shows geometrical isomerism. (i) $[Cr(H_2O)_4Cl_2]^{+}$ (ii) $[Pt(NH_3)_3Cl]$ (iii) $[Co(NH_3)_6]^{3+}$ (iv)…Preview
  8. Q8The CFSE for octahedral $[CoCl_6]^{4-}$ is $18,000\ \text{cm}^{-1}$. The CFSE for tetrahedral $[CoCl_4]^{2-}$ will be (i) $18,000\ \text{cm}…Preview
  9. Q9Due to the presence of ambidentate ligands coordination compounds show isomerism. Palladium complexes of the type $[Pd(C_6H_5)_2(SCN)_2]$ an…Preview
  10. Q10The compounds $[Co(SO_4)(NH_3)_5]Br$ and $[Co(SO_4)(NH_3)_5]Cl$ represent (i) linkage isomerism (ii) ionisation isomerism (iii) coordination…Preview
  11. Q11A chelating agent has two or more than two donor atoms to bind to a single metal ion. Which of the following is not a chelating agent? (i) t…Preview
  12. Q12Which of the following species is not expected to be a ligand? (i) $NO$ (ii) $NH_4^{+}$ (iii) $NH_2CH_2CH_2NH_2$ (iv) $CO$Preview
  13. Q13What kind of isomerism exists between $[Cr(H_2O)_6]Cl_3$ (violet) and $[Cr(H_2O)_5Cl]Cl_2 \cdot H_2O$ (greyish-green)? (i) linkage isomerism…Preview
  14. Q14IUPAC name of $[Pt(NH_3)_2Cl(NO_2)]$ is: (i) Platinum diaminechloronitrite (ii) Chloronitrito-N-ammineplatinum (II) (iii) Diamminechloridoni…Preview
  15. Q15Arrange the following complexes in the increasing order of conductivity of their solution: $[Co(NH_3)_3Cl_3]$, $[Co(NH_3)_4Cl_2]Cl$, $[Co(NH…Preview
  16. Q16A coordination compound $CrCl_3 \cdot 4H_2O$ precipitates silver chloride when treated with silver nitrate. The molar conductance of its sol…Preview
  17. Q17A complex of the type $[M(AA)_2X_2]^{n+}$ is known to be optically active. What does this indicate about the structure of the complex? Give…Preview
  18. Q18Magnetic moment of $[MnCl_4]^{2-}$ is 5.92 BM. Explain giving reason.Preview
  19. Q19On the basis of crystal field theory explain why Co(III) forms paramagnetic octahedral complex with weak field ligands whereas it forms diam…Preview
  20. Q20Why are low spin tetrahedral complexes not formed?Preview
  21. Q21Give the electronic configuration of the following complexes on the basis of Crystal Field Splitting theory. $[CoF_6]^{3-}$, $[Fe(CN)_6]^{4-…Preview
  22. Q22Explain why $[Fe(H_2O)_6]^{3+}$ has magnetic moment value of 5.92 BM whereas $[Fe(CN)_6]^{3-}$ has a value of only 1.74 BM.Preview
  23. Q23Arrange following complex ions in increasing order of crystal field splitting energy ($\Delta_O$): $[Cr(Cl)_6]^{3-}$, $[Cr(CN)_6]^{3-}$, $[C…Preview
  24. Q24Why do compounds having similar geometry have different magnetic moment?Preview
  25. Q25$CuSO_4 \cdot 5H_2O$ is blue in colour while $CuSO_4$ is colourless. Why?Preview
  26. Q26Name the type of isomerism when ambidentate ligands are attached to central metal ion. Give two examples of ambidentate ligands.Preview
  27. Q27Using crystal field theory, draw energy level diagram, write electronic configuration of the central metal atom/ion and determine the magnet…Preview
  28. Q28Using valence bond theory, explain the following in relation to the complexes given below: $[Mn(CN)_6]^{3-}$, $[Co(NH_3)_6]^{3+}$, $[Cr(H_2O…Preview
  29. Q29$CoSO_4Cl \cdot 5NH_3$ exists in two isomeric forms 'A' and 'B'. Isomer 'A' reacts with $AgNO_3$ to give white precipitate, but does not rea…Preview
  30. Q30What is the relationship between observed colour of the complex and the wavelength of light absorbed by the complex?Preview
  31. Q31Why are different colours observed in octahedral and tetrahedral complexes for the same metal and same ligands?Preview
  32. Q32Atomic number of Mn, Fe and Co are 25, 26 and 27 respectively. Which of the following inner orbital octahedral complex ions are diamagnetic?…Preview
  33. Q33Atomic number of Mn, Fe, Co and Ni are 25, 26, 27 and 28 respectively. Which of the following outer orbital octahedral complexes have same n…Preview
  34. Q34Which of the following options are correct for $[Fe(CN)_6]^{3-}$ complex? (i) $d^2sp^3$ hybridisation (ii) $sp^3d^2$ hybridisation (iii) par…Preview
  35. Q35An aqueous pink solution of cobalt(II) chloride changes to deep blue on addition of excess of HCl. This is because ____________. (i) $[Co(H_…Preview
  36. Q36Which of the following complexes are homoleptic? (i) $[Co(NH_3)_6]^{3+}$ (ii) $[Co(NH_3)_4Cl_2]^{+}$ (iii) $[Ni(CN)_4]^{2-}$ (iv) $[Ni(NH_3)…Preview
  37. Q37Which of the following complexes are heteroleptic? (i) $[Cr(NH_3)_6]^{3+}$ (ii) $[Fe(NH_3)_4Cl_2]^{+}$ (iii) $[Mn(CN)_6]^{4-}$ (iv) $[Co(NH_…Preview
  38. Q38Identify the optically active compounds from the following: (i) $[Co(en)_3]^{3+}$ (ii) trans-$[Co(en)_2Cl_2]^{+}$ (iii) cis-$[Co(en)_2Cl_2]^…Preview
  39. Q39Identify the correct statements for the behaviour of ethane-1,2-diamine as a ligand. (i) It is a neutral ligand. (ii) It is a didentate liga…Preview
  40. Q40Which of the following complexes show linkage isomerism? (i) $[Co(NH_3)_5(NO_2)]^{2+}$ (ii) $[Co(H_2O)_5CO]^{3+}$ (iii) $[Cr(NH_3)_5SCN]^{2+…Preview
  41. Q41Match the complex ions given in Column I with the colours given in Column II and assign the correct code: Column I (Complex ion): A. $[Co(NH…Preview
  42. Q42Match the coordination compounds given in Column I with the central metal atoms given in Column II and assign the correct code: Column I (Co…Preview
  43. Q43Match the complex ions given in Column I with the hybridisation and number of unpaired electrons given in Column II and assign the correct c…Preview
  44. Q44Match the complex species given in Column I with the possible isomerism given in Column II and assign the correct code: Column I (Complex sp…Preview
  45. Q45Match the compounds given in Column I with the oxidation state of cobalt present in it (given in Column II) and assign the correct code: Col…Preview
  46. Q46Assertion: Toxic metal ions are removed by the chelating ligands. Reason: Chelate complexes tend to be more stable. (i) Assertion and reason…Preview
  47. Q47Assertion: $[Cr(H_2O)_6]Cl_2$ and $[Fe(H_2O)_6]Cl_2$ are reducing in nature. Reason: Unpaired electrons are present in their d-orbitals. (i)…Preview
  48. Q48Assertion: Linkage isomerism arises in coordination compounds containing ambidentate ligand. Reason: Ambidentate ligand has two different do…Preview
  49. Q49Assertion: Complexes of $MX_6$ and $MX_5L$ type (X and L are unidentate) do not show geometrical isomerism. Reason: Geometrical isomerism is…Preview
  50. Q50Assertion: $[Fe(CN)_6]^{3-}$ ion shows magnetic moment corresponding to two unpaired electrons. Reason: Because it has $d^2sp^3$ type hybrid…Preview

Sample & Board Papers

Sample papers and previous-year board questions for this subject.