Class 12 Chemistry - Chapter Coordination Compounds NCERT Solutions | Write all the geometrical isomers of [Pt

[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

What are micelles? Give an example of a micellers system.

Why do we require artificial sweetening agents?

Explain why inspite of nearly the same electronegativity, oxygen forms hydrogen bonding while chlorine does not.

Explain briefly how +2 state becomes more and more stable in the first half of the first row transition elements with increasing atomic number?

What are monosaccharides?

In the following pairs of halogen compounds, which compound undergoes faster S_N1 reaction?

How would you account for the following:

(i) Of the d⁴ species, Cr²⁺ is strongly reducing while manganese (III) is strongly oxidising.

(ii) Cobalt (II) is stable in aqueous solution but in the presence of complexing reagents it is easily oxidised.

(iii) The d¹ configuration is very unstable in ions.

How will you convert?

(i) Benzene into aniline

(ii) Benzene into N, N-dimethylaniline

(iii) Cl-(CH₂)₄-Cl into hexan-1, 6-diamine?

Why does the conductivity of a solution decrease with dilution?

How will you convert:

(i) Ethanoic acid into methanamine

(ii) Hexanenitrile into 1-aminopentane

(iii) Methanol to ethanoic acid

(iv) Ethanamine into methanamine

(v) Ethanoic acid into propanoic acid

(vi) Methanamine into ethanamine

(vii) Nitromethane into dimethylamine

(viii) Propanoic acid into ethanoic acid