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No of ions will Ni(CO)4 have after dissociation?
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No of ions will Ni(CO)4 have after dissociation?
Number of ions in Ni(CO)4 after dissociation
Ni(CO)4 is a coordination complex consisting of a central nickel atom bonded to four carbon monoxide ligands. When this complex dissociates, it forms ions based on the charges of the individual components.

Initial composition of Ni(CO)4
- Ni(CO)4 is a neutral molecule with a total charge of 0.
- The nickel atom has a formal oxidation state of 0, while each CO ligand contributes a -1 charge.

Dissociation of Ni(CO)4
- Upon dissociation, Ni(CO)4 can form two possible types of ions:
1. Ni2+ ion: This ion is formed when the nickel atom loses two electrons, resulting in a 2+ charge.
2. 4 CO ligands: These ligands can each form a carbonyl anion (CO-) by gaining an electron, resulting in a total of four CO- ions.

Final composition of ions
- After dissociation, Ni(CO)4 will yield one Ni2+ ion and four CO- ions.
- The Ni2+ ion has a charge of 2+, while each CO- ion carries a charge of -1.
In conclusion, after dissociation, Ni(CO)4 will result in a total of 1 Ni2+ ion and 4 CO- ions, bringing the total charge of the system to 0.
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Titrations are one of the methods we can use to discover the precise concentrations of solution. A typical titration involves adding a solution from a burette to another solution in a flask. The endpoint of the titration is found by watching a colour change taking place. However, a problem arises when a suitable indicator cannot be found, or when the colour changes involved are unclear. In cases redox potential may sometimes come to the rescue.A particularly well known example (Fig.1) is a method of discovering the concentration of iron in a solution by titrating them with a solution of cerium (IV). The redox potential that areof interest here are EFe3+/Fe2+ = + 0.77 V and ECe4+/Ce3+ = + 1.61 V. These tell us that cercium (IV) ions are the oxidizing agents, and iron (II) ions are the reducing agent. They should react according to the equationFe2+ (aq) + Ce4+ (aq) Fe3+ (aq) + Ce3+ (aq)Now imagine that we know the concentration of the cerium (IV) ions solution in the burette. We want to measure the concentration of the iron (II) solution. If we add just one drop of the cerium (IV) solution from the bruette, some of the iron (II) ions will be oxidised. As a consequence the beaker would now contain a large number of unreacted ions, but also some iron (III) ions as well. All of the cerium (III). The solution in the beaker now represents an iron(III)/iron(II) half cell, although not at standard conditions. Thus the e.m.f. of the cell will be near, but not equal, to EFe3+/Fe2+.to ad cerium (IV) solution, the number of iron (II) ions is gradually reduced and eventually only a very few are left (Tabl e).At this stage the next few drops of cerium (IV) solution convert all the remaining iron (II) ions into iron (III), and some of the cerium (IV) ions are left unreacted. Once this happens we no longer ions and a smaller number of cerium (IV) ions. The solution in the beaker now behaves as a cerium (IV)/cerium (III) half-cell (although not a standard one).Just before all the iron (II) ions are converted into iron (III) we have a cell with an e.m.f.of around + 0.77 V. After all the iron (II) ions are oxidised, we have a cell with an e.m.f. of about + 1.61 V. This rapid rise in e.m.f. occurs with the addition of hust one drop of cerium (IV) solution. You should be able to understand why a graph of cell e.m.f. against volume ofcerium (IV) solution added looks like that of Fig. 2. The end point of the titration can be read from the graph and the concentration of the iron (II) solution calculated in the usual wayQ.The cell shown below was set upWhat would be the cell e.m.f.? If potassium cyanide solution were added to the left hand half cell (with due care!), what would you expect to happen to the e.m.f. of the cell? E Br2/Br- = 1.07V and use data of previousquestion, if required.

Titrations are one of the methods we can use to discover the precise concentrations of solution. A typical titration involves adding a solution from a burette to another solution in a flask. The endpoint of the titration is found by watching a colour change taking place. However, a problem arises when a suitable indicator cannot be found, or when the colour changes involved are unclear. In cases redox potential may sometimes come to the rescue.A particularly well known example (Fig.1) is a method of discovering the concentration of iron in a solution by titrating them with a solution of cerium (IV). The redox potential that areof interest here are EFe3+/Fe2+ = + 0.77 V and ECe4+/Ce3+ = + 1.61 V. These tell us that cercium (IV) ions are the oxidizing agents, and iron (II) ions are the reducing agent. They should react according to the equationFe2+ (aq) + Ce4+ (aq) Fe3+ (aq) + Ce3+ (aq)Now imagine that we know the concentration of the cerium (IV) ions solution in the burette. We want to measure the concentration of the iron (II) solution. If we add just one drop of the cerium (IV) solution from the bruette, some of the iron (II) ions will be oxidised. As a consequence the beaker would now contain a large number of unreacted ions, but also some iron (III) ions as well. All of the cerium (III). The solution in the beaker now represents an iron(III)/iron(II) half cell, although not at standard conditions. Thus the e.m.f. of the cell will be near, but not equal, to EFe3+/Fe2+.to ad cerium (IV) solution, the number of iron (II) ions is gradually reduced and eventually only a very few are left (Tabl e).At this stage the next few drops of cerium (IV) solution convert all the remaining iron (II) ions into iron (III), and some of the cerium (IV) ions are left unreacted. Once this happens we no longer ions and a smaller number of cerium (IV) ions. The solution in the beaker now behaves as a cerium (IV)/cerium (III) half-cell (although not a standard one).Just before all the iron (II) ions are converted into iron (III) we have a cell with an e.m.f.of around + 0.77 V. After all the iron (II) ions are oxidised, we have a cell with an e.m.f. of about + 1.61 V. This rapid rise in e.m.f. occurs with the addition of hust one drop of cerium (IV) solution. You should be able to understand why a graph of cell e.m.f. against volume ofcerium (IV) solution added looks like that of Fig. 2. The end point of the titration can be read from the graph and the concentration of the iron (II) solution calculated in the usual wayQ.When an ion is converted into a complex ion, the redox potential changes. You can see this in the case of the e.m.f. of the iron (III)/ iron (II) system (+ 0.77 V) and the hexacyanoferrate (III)/ hexacyanoferrate (II) system (+0.36 V). The cyanide ion is said to stabilize the oxidation state of the iorn. If you were to make up a cell What would be the e.m.f. and what would be the cell reaction?

Titrations are one of the methods we can use to discover the precise concentrations of solution. A typical titration involves adding a solution from a burette to another solution in a flask. The endpoint of the titration is found by watching a colour change taking place. However, a problem arises when a suitable indicator cannot be found, or when the colour changes involved are unclear. In cases redox potential may sometimes come to the rescue.A particularly well known example (Fig.1) is a method of discovering the concentration of iron in a solution by titrating them with a solution of cerium (IV). The redox potential that areof interest here are EFe3+/Fe2+ = + 0.77 V and ECe4+/Ce3+ = + 1.61 V. These tell us that cercium (IV) ions are the oxidizing agents, and iron (II) ions are the reducing agent. They should react according to the equationFe2+ (aq) + Ce4+ (aq) Fe3+ (aq) + Ce3+ (aq)Now imagine that we know the concentration of the cerium (IV) ions solution in the burette. We want to measure the concentration of the iron (II) solution. If we add just one drop of the cerium (IV) solution from the bruette, some of the iron (II) ions will be oxidised. As a consequence the beaker would now contain a large number of unreacted ions, but also some iron (III) ions as well. All of the cerium (III). The solution in the beaker now represents an iron(III)/iron(II) half cell, although not at standard conditions. Thus the e.m.f. of the cell will be near, but not equal, to EFe3+/Fe2+.to ad cerium (IV) solution, the number of iron (II) ions is gradually reduced and eventually only a very few are left (Tabl e).At this stage the next few drops of cerium (IV) solution convert all the remaining iron (II) ions into iron (III), and some of the cerium (IV) ions are left unreacted. Once this happens we no longer ions and a smaller number of cerium (IV) ions. The solution in the beaker now behaves as a cerium (IV)/cerium (III) half-cell (although not a standard one).Just before all the iron (II) ions are converted into iron (III) we have a cell with an e.m.f.of around + 0.77 V. After all the iron (II) ions are oxidised, we have a cell with an e.m.f. of about + 1.61 V. This rapid rise in e.m.f. occurs with the addition of hust one drop of cerium (IV) solution. You should be able to understand why a graph of cell e.m.f. against volume ofcerium (IV) solution added looks like that of Fig. 2. The end point of the titration can be read from the graph and the concentration of the iron (II) solution calculated in the usual wayQ.Imagine you were given a solution of potassium dichromate (VI) in a beaker, and a solution of iron (II) sulphate in a burette. You do not know the concentration of dichromate (VI) ions, but the concentration of the iron (II) solution is known. Your task is to carry out a redox titration using the two solutions in order to determine the concentration of dichromate(VI) ions. Sketch a graph how the e.m.f. changes in the course of above titration. E Cr2O2-7/Cr3+ = 1.33 V, EFe3+/Fe2+ = 0.77 V.

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No of ions will Ni(CO)4 have after dissociation?
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