2.335 g of compound X (empirical formal CoH12N4Cl3) upon treatment with excess AgNO3 solution produces 1.435 g of a white precipitate. The primary and secondary valences of cobalt in compound X, respectively are:
[Given Atomic mass: Co = 59, Cl = 35.5, Ag = 108]
1. | 3, 6 | 2. | 3, 4 |
3. | 2, 4 | 4. | 4, 3 |
If an excess of solution is added to 100 mL of a 0.024 M solution of dichlorobis (ethylenediamine) cobalt (III) chloride, then the number of moles of AgCl that will be precipitated is:
1. | 0.0012 | 2. | 0.0016 |
3. | 0.0024 | 4. | 0.0048 |
When 0.1 mol of CoCl3(NH3)5 is treated with an excess of AgNO3, 0.2 mol of AgCl is obtained. The conductivity of the solution will correspond to:
1. | 1:3 electrolyte | 2. | 1:2 electrolyte |
3. | 1:1 electrolyte | 4. | 3:1 electrolyte |
The correct order of the stoichiometrics of AgCl formed when AgNO3 in excess is treated with the complexes:- CoCl3.6NH3, CoCl3.5NH3, CoCl3.4NH3, respectively, is :
1. 1 AgCl, 3 AgCl, 2 AgCl
2. 3 AgCl, 1 AgCl, 2 AgCl
3. 3 AgCl, 2 AgCl, 1 AgCl
4. 2 AgCl, 3AgCl, 1 AgCl
The sum of the coordination number and oxidation number of the metal M in the complex [M(en)2(C2O4)]Cl is:
1. | 9 | 2. | 6 |
3. | 7 | 4. | 8 |
Cobalt(III) chloride forms several octahedral complexes with ammonia.
A compound among the following that does not give a test for chloride ions with silver nitrate at 25 °C is:
1. | CoCl3. 3NH3 | 2. | CoCl3. 4NH3 |
3. | CoCl3. 5NH3 | 4. | CoCl3. 6NH3 |
1. | 0.002 | 2. | 0.003 |
3. | 0.01 | 4. | 0.001 |
If 1/3rd of the total chlorine of the compound is precipitated by adding AgNO3 to its aqueous solution, then the most likely structure of CrCl3.6H2O among the following is:
1. | CrCl3.6H2O | 2. | [Cr(H2O)3Cl3](H2O)3 |
3. | [CrCl2(H2O)4]Cl.2H2O | 4. | [CrCl.(H2O)5]Cl2.H2O |
The existence of two different coloured complexes with the composition of [Co(NH3)4Cl2]+ is due to:
1. | Linkage isomerism | 2. | Geometrical isomerism |
3. | Coordination isomerism | 4. | Ionisation isomerism |