Advertisements
Advertisements
Question
The stabilisation of coordination compounds due to chelation is called the chelate effect. Which of the following is the most stable complex species?
Options
\[\ce{[Fe(CO)5]}\]
\[\ce{[Fe(CN)6]^{3-}}\]
\[\ce{[Fe(C2O4)3]^{3-}}\]
\[\ce{[Fe(H2O)6]^{3+}}\]
Advertisements
Solution
\[\ce{[Fe(C2O4)3]^{3-}}\]
Explanation:
Chelation (formation of cycle by linkage between metal ion and ligand) stabilizes the coordination compound. The ligand which chelates the metal ion are known as chelating ligand.
Here, only \[\ce{[Fe(C2O4)3]^{3-}}\] is a coordination compound which contains oxalate ion as a chelating ligand.
Hence, it stabilizes coordination compound by chelating \[\ce{Fe^{3+}}\] ion.
APPEARS IN
RELATED QUESTIONS
Write IUPAC name of the following Complex [Cr(NH3)3Cl3]
Complete the following reactions
NH3+3Cl2(excess) ---->
Write the structures of compounds A, B and C in the following reactions:

Write the IUPAC name of the following coordination compound:
[PtCl2(NH3)4][PtCl4]
The ligand triethylenetetramine is _______.
The oxidation number of Fe in K4[Fe(CN)6] is ____________.
When 0.1 mol \[\ce{CoCl3 (NH3)5}\] is treated with excess of \[\ce{AgNO3}\], 0.2 mol of \[\ce{AgCl}\] are obtained. The conductivity of solution will correspond to ______.
Identify 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 ligand.
(iii) It is a chelating ligand.
(iv) It is a unidentate ligand.
A complex of the type \[\ce{[M(AA)2X2]^{n+}}\] is known to be optically active. What does this indicate about the structure of the complex? Give one example of such complex.
Match the complex ions given in Column I with the colours given in Column II and assign the correct code:
| Column I (Complex ion) | Column II (Colour) |
| A. \[\ce{[Co(NH3)6]^{3+}}\] | 1. Violet |
| B. \[\ce{[Ti(H2O)6]^{3+}}\] | 2. Green |
| C. \[\ce{[Ni(H2O)6]^{2+}}\] | 3. Pale blue |
| D. \[\ce{(Ni(H2O)4 (en)]^{2+} (aq)}\] | 4. Yellowish orange |
| 5. Blue |
Match the compounds given in Column I with the oxidation state of cobalt present in it (given in Column II) and assign the correct code:
| Column I (Compound) | Column II (Oxidation state of Co) |
| A. \[\ce{[Co(NCS)(NH3)5](SO3)}\] | 1. + 4 |
| B. \[\ce{[Co(NH3)4 CL2]SO4}\] | 2. 0 |
| C. \[\ce{Na4[Co(S2O3)3]}\] | 3. + 1 |
| D. \[\ce{[Co2(CO)8]}\] | 4. + 2 |
| 5. + 3 |
Assertion: \[\ce{Cr(H2O)6]Cl2 and [Fe(H2O)6]Cl2}\] are reducing in nature.
Reason: Unpaired electrons are present in their d-orbitals.
The nature of hybridisation in the ammonia molecule is
What are Heteroleptic complexes?
Does ionization isomer for the following compound exist? Justify your answer.
\[\ce{Hg[Co(SCN)4]}\]
What is meant by the chelate effect? Give an example.
What is meant by the chelate effect? Give an example.
Give two examples of didentate ligands.
