Coordination Compounds Mock Test – Class 12 Chemistry
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Coordination Compounds Mock Test – Class 12 Chemistry

Progressive Test — Guest First Round

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Coordination Compounds – Progressive Test

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1. An octahedral entity of type has only one geometrical arrangement because:

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2. An iron atom has the ground-state configuration . The -electron configuration of is:

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3. For the stepwise formation equilibrium

the constant measures:

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4. Study the proposed octahedral CFSE values.

Row Configuration Proposed CFSE
P
Q
R
S

The inconsistent row is:

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5. The usual valence bond reasoning for a strong-field octahedral complex follows the sequence:

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6. Three statements describe how denticity affects coordination. Identify the valid combination.
Statement I: An ambidentate ligand may possess two potential donor atoms.
Statement II: A bidentate ligand normally uses two donor atoms simultaneously to bind one metal centre.
Statement III: Each ambidentate ligand necessarily contributes to the coordination number.
The valid statements are:

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7. Study the charge-balance table.

Compound Coordination-entity charge Counter ions per formula unit
P. Three
Q. Four
R. One
S. Two

The inconsistent row is:

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8. An octahedral ion has the configuration . Its CFSE is:

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9. Consider the following statements about coordination nomenclature.
Statement I: The bracketed coordination entity is named as one unit.
Statement II: The oxidation state of the central metal is written using a Roman numeral.
Statement III: Counter ions are always omitted from the complete compound name.
The valid statements are:

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10. Carbon monoxide forms strong complexes with metals in low oxidation states and participates in metal-to-ligand back-bonding. Why is this behaviour not fully described by elementary crystal field theory?

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11. The ligand names for , , , and , in that order, are:

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12. A student analyses and writes, “Manganese has oxidation state , so the complex has unpaired electrons.” Which correction is most appropriate?

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13. In valence bond theory, hybridisation of the central metal orbitals is mainly used to explain:

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14. Why are the octahedral orbital-energy coefficients and , rather than equal values?

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15. A graph for an octahedral complex shows increasing along the horizontal axis. What magnetic change is expected as the system moves from to ?

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16. Study the octahedral arrangements.

Row Relationship between two identical ligands Assigned form
P Adjacent positions Cis
Q Angle of Cis
R Opposite positions Trans
S Angle of Cis

The inconsistent row is:

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17. Assign the IUPAC name to :

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18. Electron pairing may occur before hybridisation primarily to:

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19. A graph has absorbed wavelength on the horizontal axis and crystal-field splitting on the vertical axis. Which curve best represents the relation between them?

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20. A proposed name for contains cobalt(II). The most accurate diagnosis is:

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21. An octahedral complex of the type can show:

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22. The naming order of differs from that of because:

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23. A metal ion is initially surrounded by six separate monodentate ligands. They are replaced by one ligand, and all six donor atoms of bind to the metal. The replacement changes:

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24. Two colourless crystalline solids and are dissolved separately. Every simple ion expected from the constituent salts of can be detected independently. In the solution of , one bracketed metal–ligand ion remains the principal metal-containing species. The sound conclusion is:

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25. A theory predicts that a complex is octahedral and paramagnetic but cannot account satisfactorily for its absorption wavelength. The theory being used is most likely:

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26. Study the proposed classifications.

Row Metal ion -electron count Ordinary - transition
P Absent
Q Absent
R Absent
S Always the only source of intense colour

The inconsistent row is:

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27. Assertion: donation and back-bonding in a metal carbonyl reinforce one another.
Reason: donation increases electron density at the metal for back donation, while back donation removes some metal electron density and allows continued ligand-to-metal donation.

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28. A tetrahedral ion has configuration . Which set of properties is correct?

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29. The pair and differs because:

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30. In , the coordination sphere contains:

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31. A student says, “The colour is an unchanging property of the metal ion, so every complex containing that ion must have the same colour.” The best correction is:

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32. A four-coordinate complex is experimentally diamagnetic. Another complex of the same metal ion is paramagnetic with two unpaired electrons. The most consistent geometries of the two complexes are respectively:

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33. Choose the IUPAC name for :

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34. Study the proposed magnetic-property assignments.

Row Octahedral configuration Spin description Unpaired electrons Approximate moment
P High-spin
Q Low-spin
R Low-spin
S High-spin

The inconsistent row is:

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35. Complexes and contain the same metal ion in the same oxidation state and have the same geometry. The ligand in produces a stronger field than the ligand in . Which conclusion is most reasonable?

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36. Crystal field theory differs from simple valence bond theory because:

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37. Assertion: Outer-orbital octahedral complexes commonly have more unpaired electrons than corresponding paired inner-orbital complexes of the same ion.
Reason: Formation of hybrid orbitals does not require two vacant inner orbitals.

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38. Consider the following statements about coordination catalysts.
Statement I: A substrate may bind temporarily to the metal centre.
Statement II: Coordination can orient reacting molecules favourably.
Statement III: A catalyst must be permanently converted into the final product.
Statement IV: Ligand substitution may create a vacant site for substrate binding.
The valid statements are:

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39. A member of the cobalt(III) ammine series has the general formula

where may have values from to . The total number of dissolved species produced per formula unit on ideal dissolution is:

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40. Two ligands in an octahedral entity are replaced by one ethane-1,2-diamine ligand, represented by , without changing the coordination number. The resulting formula and total number of ligand molecules are:

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41. Assertion: In the name of , the coordination entity is named before chloride.
Reason: The bracketed entity is a cation, and a cation is named before an anion.

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42. Study the ligand-name table.

Row Ligand Proposed ligand name
P Ammine
Q Aqua
R Cyanide
S Carbonyl

The inconsistent row is:

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43. In the equilibrium

why is formation of the chelate complex often favoured?

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44. The platinum centre in cisplatin follows the sequence:

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45. Use the arrangement described below: structure and structure are mirror images. No rotation or translation can make every ligand position in coincide with the corresponding position in . The pair represents:

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46. Study the oxidation-state assignments below.

Coordination entity Assigned metal oxidation state
P.
Q.
R.
S.

The inconsistent row is:

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47. Separate aqueous solutions of Mohr’s salt and are treated with a reagent that tests for free . The expected observation is that:

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48. Which observation correctly identifies cis-?

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49. Complexes and both have the form and are compared under the same conditions. Their overall formation constants are and . Which conclusion is justified?

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50. In , the oxidation states of cobalt and chromium are:

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