Class 12 Chemistry - Chapter Coordination Compounds NCERT Solutions | What is the coordination entity formed w

[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]

The oxidation number of cobalt in K[Co(CO)₄] is

(i) +1

(ii) +3

(iii) -1

(iv) -3

[Cr(NH₃)₆]³⁺ is paramagnetic while [Ni(CN)₄]^2- is diamagnetic.  Explain why?

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

Can PCl₅ act as an oxidising as well as a reducing agent? Justify.

Nalorphene (C₁₉H₂₁NO₃), similar to morphine, is used to combat withdrawal symptoms in narcotic users. Dose of nalorphene generally given is 1.5 mg. Calculate the mass of 1.5 x 10^-3m aqueous solution required for the above dose.

Why is ICl more reactive than I₂?

Out of C and CO, which is a better reducing agent for ZnO ?

Explain how vacancies are introduced in an ionic solid when a cation of higher valence is added as an impurity in it.

Why is it essential to wash the precipitate with water before estimating it quantitatively?

An organic compound contains 69.77% carbon, 11.63% hydrogen and rest oxygen. The molecular mass of the compound is 86. It does not reduce Tollens' reagent but forms an addition compound with sodium hydrogensulphite and give positive iodoform test. On vigorous oxidation it gives ethanoic and propanoic acid. Write the possible structure of the compound.

What are nucleic acids? Mention their two important functions.

How does the presence of double bonds in rubber molecules influence their structure and reactivity?

Write reactions of the final alkylation product of aniline with excess of methyl iodide in the presence of sodium carbonate solution.