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Ligands are broadly classified into two ...

Ligands are broadly classified into two classes classical and non-classical ligands, depending on their donor annd acceptor ability. Classical ligands form classical complexes while non-classical ligands form non-classical complex. Bonding mechanism in non-classical is called synergic bonding.
Q. Synergic bonding is absent in:

A

`[Mo(CO)_(6)]`

B

`[Cr(CO)_(3)(B_(3)N_(3)H_(6)]`

C

`[Sc(CO)_(6)]^(3+)`

D

`[Ni(CN)_(4)]^(4-)`

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The correct Answer is:
To determine where synergic bonding is absent, we need to analyze the ligands and the oxidation states of the metal ions involved. Here's a step-by-step solution: ### Step 1: Understand Synergic Bonding Synergic bonding involves the back donation of electrons from the metal ion to the anti-bonding orbitals of the ligands. This typically occurs when the metal has available d-electrons that can be donated. **Hint:** Remember that synergic bonding requires the presence of d-electrons in the metal ion. ### Step 2: Identify the Metal Ions and Their Oxidation States We need to look at the metal ions in the given options and their oxidation states: - **Molybdenum (Mo)**: Neutral ligand, oxidation state = 0. - **Chromium (Cr)**: Neutral ligand, oxidation state = 0. - **Scandium (Sc)**: This is a +3 oxidation state, which means it has lost its 3d and 4s electrons. - **Nickel (Ni)**: Neutral ligand, oxidation state = 0. **Hint:** Check the oxidation states of each metal ion to see if they have available d-electrons. ### Step 3: Determine Electron Configurations Next, we write the electron configurations for the relevant metal ions: - **Molybdenum (Mo)**: [Kr] 4d5 5s1 - **Chromium (Cr)**: [Ar] 4s1 3d5 - **Scandium (Sc)**: [Ar] 4s2 3d1 (but in +3 state, it becomes empty) - **Nickel (Ni)**: [Ar] 4s2 3d8 **Hint:** The key here is to identify which metal ion has no d-electrons available for back donation. ### Step 4: Analyze Each Case for Synergic Bonding - **Molybdenum**: Has d-electrons available for synergic bonding. - **Chromium**: Also has d-electrons available for synergic bonding. - **Scandium**: In the +3 oxidation state, it has no d-electrons available (3d0), hence no synergic bonding. - **Nickel**: Has d-electrons available for synergic bonding. **Hint:** Focus on the metal ion that has no d-electrons left after ionization. ### Step 5: Conclusion From the analysis, we conclude that synergic bonding is absent in **Scandium (Sc)** in its +3 oxidation state. **Final Answer:** Synergic bonding is absent in Scandium (option C).

To determine where synergic bonding is absent, we need to analyze the ligands and the oxidation states of the metal ions involved. Here's a step-by-step solution: ### Step 1: Understand Synergic Bonding Synergic bonding involves the back donation of electrons from the metal ion to the anti-bonding orbitals of the ligands. This typically occurs when the metal has available d-electrons that can be donated. **Hint:** Remember that synergic bonding requires the presence of d-electrons in the metal ion. ### Step 2: Identify the Metal Ions and Their Oxidation States ...
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Ligands are broadly classified into two classes classical and non-classical ligands, depending on their donor annd acceptor ability. Classical ligands form classical complexes while non-classical ligands form non-classical complex. Bonding mechanism in non-classical is called synergic bonding. Q. Which is not pi -acceptor ligand?

Ligands are broadly classified into two classes classical and non-classical ligands, depending on their donor annd acceptor ability. Classical ligands form classical complexes while non-classical ligands form non-classical complex. Bonding mechanism in non-classical is called synergic bonding. Q. Which is not pi -acceptor ligand?

Ligands are broadly classified into two classes classical and non-classical ligands, depending on their donor annd acceptor ability. Classical ligands form classical complexes while non-classical ligands form non-classical complex. Bonding mechanism in non-classical is called synergic bonding. Q. In compound [M(CO)_(n)]^(x) , the correct match for highest 'M-C' bond length for given M, n and z respectively:

Ligands are broadly classified into two classes classical and non-classical ligands, depending on their donor annd acceptor ability. Classical ligands form classical complexes while non-classical ligands form non-classical complex. Bonding mechanism in non-classical is called synergic bonding. Q. In compound [M(CO)_(n)]^(z) , the correct match for highest 'M-C' bond length for given M, n and z respectively:

The pi acid ligand which uses it d-orbital during synergic bonding in its complex compound.

Assertion Chelates are relatively more stable than non-cheltated complexes Reason Complexes containing ligands which can be easily replaced by other ligands are called labile complexes .

Consider the two complexation equilibria in aqueous solution, between the cobalt (II) ion Co^(2+) (aq) and ethylenediamine (en) on the one hand and ammonia NH_(3) on the other. [Co(H_(2)O)_(6)]^(2+)+6NH_(3)hArr[Co(NH_(3))_(6)]^(2+)+6H_(2)O ...(1) [Co(H_(2)O_(6))]^(2+)+3enhArr[Co(en)_(3)]^(2+)+6H_(2)O ..(2) Electronicaly, the ammonia and en ligands are very similar, since both bond through N and since the liwis base strengths of their nitrogen atoms are similar. This means that DeltaH^(@) must be very similar for the two reactions, since six Co-N bonds are formed in each case. Interestingly however, the equilibrium constant is 100,000 times larger for the second reaction than it is for the first. This is the so called chelate effect: "the enhanced affinity of chelating ligands for a metal ion compared to similar non-chelating (monodentate) ligands for the same metal". The chelate effect is entropy-driven. Q. Which of the following can be classified as a chelating ligand?

Consider the two complexation equilibria in aqueous solution, between the cobalt (II) ion Co^(2+) (aq) and ethylenediamine (en) on the one hand and ammonia NH_(3) on the other. [Co(H_(2)O)_(6)]^(2+)+6NH_(3)hArr[Co(NH_(3))_(6)]^(2+)+6H_(2)O ...(1) [Co(H_(2)O_(6))]^(2+)+3enhArr[Co(en)_(3)]^(2+)+6H_(2)O ..(2) Electronicaly, the ammonia and en ligands are very similar, since both bond through N and since the liwis base strengths of their nitrogen atoms are similar. This means that DeltaH^(@) must be very similar for the two reactions, since six Co-N bonds are formed in each case. Interestingly however, the equilibrium constant is 100,000 times larger for the second reaction than it is for the first. This is the so called chelate effect: "the enhanced affinity of chelating ligands for a metal ion compared to similar non-chelating (monodentate) ligands for the same metal". The chelate effect is entropy-driven. Q. What may be main reason for reaction (2) having relatively such a large equilibrium constant?

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: Value of CFSE depends upon nature of ligand and a spectrochemical series has been made experimentally, for tetrahedral complexes, Delta is about 4/9 times to Delta_(0) (CFSE for octahedral complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. Cr^(3+) form four complexes with four different ligands which are [Cr(Cl)_(6)]^(3-), [Cr(H_(2)O)_(6)]^(3+) , [Cr(NH_(3))_(6)]^(3+) and [Cr(CN)_(6)]^(3-) , the order of CFSE (Delta_(0)) in these complexes in the order:

Give the number of ligand(s) which is/are non-classical ligand an pi donor as well as pi acceptor ligand CO,PH_(3), PF_(3),C_(3)H_(5)^(Θ) ,C_(5)H_(5) Θ .

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