Explain with two examples each of the following: coordination entity, ligand, coordination number, coordination polyhedron, homoleptic and heteroleptic.
(i) Coordination entity:
A coordination entity is an electrically charged radical or species carrying a positive or negative charge. In a coordination entity, the central atom or ion is surrounded by a suitable number of neutral molecules or negative ions ( called ligands). For example:
[Ni(NH3)6]2+ , [Fe(CN6)]4+ = cationic complex
[PtCl4]2- , [Ag(CN)2]- = anionic complex
[Ni(CO)4] , [Co(NH3)4 Cl2] = neutral complex
(ii) Ligands The neutral molecules or negatively charged ions that surround the metal atom in a coordination entity or a coordinal complex are known as ligands. For example,, Cl - , - OH. Ligands are usually polar in nature and possess at least one unshared pair of valence electrons.
(iii) Coordination number: The total number of ligands (either neutral molecules or negative ions) that get attached to the central metal atom in the coordination sphere is called the coordination number of the central metal atom. It is also referred to as its ligancy.
For example:
(a) In the complex, K2[PtCl6], there as six chloride ions attached to Pt in the coordinate sphere. Therefore, the coordination number of Pt is 6.
(b) Similarly, in the complex [Ni(NH3)4]Cl2, the coordination number of the central atom (Ni) is 4.
(iv) Coordination polyhedron: Coordination polyhedrons about the central atom can be defined as the spatial arrangement of the ligands that are directly attached to the central metal ion in the coordination sphere. For example: (a) (b) Tetrahedral
(v) Homoleptic complexes: These are those complexes in which the metal ion is bound to only one kind of a donor group. For eg: [Co(NH3)6]3+ , [PtCl4]2- etc.
(vi) Heteroleptic complexes: Heteroleptic complexes are those complexes where the central metal ion is bound to more than one type of a donor group. For e.g.: [Co(NH3)4 Cl2]+ , [Co(NH3)5 Cl]2+
[NiCl4]2- is paramagnetic while [Ni(CO)4] is diamagnetic though both are tetrahedral. Why?
Explain on the basis of valence bond theory that [Ni(CN)4]2- ion with square planar structure is diamagnetic and the [Ni(CN)4]2- ion with tetrahedral geometry is paramagnetic.
Draw figure to show the splitting of d orbitals in an octahedral crystal field.
Write down the IUPAC name for each of the following complexes and indicate the oxidation state, electronic configuration and coordination number. Also give stereochemistry and magnetic moment of the complex:
(i) K[Cr(H2O)2(C2O4)2].3H2O
(ii) [Co(NH3)5Cl]Cl2
(iii) CrCl3(py)3
(iv) Cs[FeCl4]
(v) K4[Mn(CN)6]
[Cr(NH3)6]3+ is paramagnetic while [Ni(CN)4]2- is diamagnetic. Explain why?
The oxidation number of cobalt in K[Co(CO)4] is
(i) +1
(ii) +3
(iii) -1
(iv) -3
Discuss the nature of bonding in metal carbonyls.
Discuss the nature of bonding in the following coordination entities on the basis of valence bond theory:
(i) [Fe(CN)6]4-
(ii) [FeF6]3-
(iii) [Co(C2O4)3]3-
(iv) [CoF6]3-
Write the formulas for the following coordination compounds:
(i) Tetraamminediaquacobalt (III) chloride
(ii) Potassium tetracyanonickelate(II)
(iii) Tris(ethane-1,2-diamine) chromium(III) chloride
(iv) Amminebromidochloridonitrito-N-platinate(II)
(v) Dichloridobis(ethane-1,2-diamine)platinum(IV) nitrate
(vi) Iron(III) hexacyanoferrate(II)
Predict the number of unpaired electrons in the square planar [Pt(CN)4]2- ion.
For the reaction R → P, the concentration of a reactant changes from 0.03 M to 0.02 M in 25 minutes. Calculate the average rate of reaction using units of time both in minutes and seconds.
(i) Write structures of different isomeric amines corresponding to the molecular formula, C4H11N
(ii) Write IUPAC names of all the isomers.
(iii) What type of isomerism is exhibited by different pairs of amines?
Why are solids rigid?
Write any two characteristics of Chemisorption.
Write the structures of the following compounds.
(i) α-Methoxypropionaldehyde
(ii) 3-Hydroxybutanal
(iii) 2-Hydroxycyclopentane carbaldehyde
(iv) 4-Oxopentanal
(v) Di-sec-butyl ketone
(vi) 4-Fluoroacetophenone
Which of the ores mentioned in Table 6.1 can be concentrated by magnetic separation method?
Why are pentahalides more covalent than trihalides?
Silver atom has completely filled d orbitals (4d10) in its ground state. How can you say that it is a transition element?
Glucose or sucrose are soluble in water but cyclohexane or benzene (simple six membered ring compounds) are insoluble in water. Explain.
Write structures of the following compounds:
(i) 2-Chloro-3-methylpentane
(ii) 1-Chloro-4-ethylcyclohexane
(iii) 4-tert. Butyl-3-iodoheptane
(iv) 1,4-Dibromobut-2-ene
(v) 1-Bromo-4-sec. butyl-2-methylbenzene
Why is Ka2 << Ka1 for H2SO4 in water?
You are given benzene, conc. H2SO4 and NaOH. Write the equations for the preparation of phenol using these reagents.
Non-stoichiometric cuprous oxide, Cu2O can be prepared in laboratory. In this oxide, copper to oxygen ratio is slightly less than 2:1. Can you account for the fact that this substance is a p-type semiconductor?
Two elements A and B form compounds having formula AB2 and AB4. When dissolved in 20 g of benzene (C6H6), 1 g of AB2 lowers the freezing point by 2.3 Kwhereas 1.0 g of AB4 lowers it by 1.3 K. The molar depression constant for benzene is 5.1 Kkg mol-1. Calculate atomic masses of A and B.
Why do gases always tend to be less soluble in liquids as the temperature is raised?
H2S, a toxic gas with rotten egg like smell, is used for the qualitative analysis. If the solubility of H2S in water at STP is 0.195 m, calculate Henry's law constant.
What is the basicity of H3PO4?
Predict the products of the following reactions:
(i)
(ii)
(iii)
(iv)
Give four uses of emulsions.
Although phenoxide ion has more number of resonating structures than carboxylate ion, carboxylic acid is a stronger acid than phenol. Why?
what is mean by coordination entity and how to find it form a complex
What are ligands?
Nice explanation.