Class 12 Chemistry - Chapter Polymers NCERT Solutions | Write the name and structure of one of t

Write the names and structures of the monomers of the following polymers:

(i) Buna-S  (ii) Buna-N

(iii) Dacron  (iv) Neoprene

What is a biodegradable polymer? Give an example of a biodegradable aliphatic polyester.

Arrange the following polymers in increasing order of their intermolecular forces.
(i) Nylon 6, 6, Buna-S, Polythene.
(ii) Nylon 6, Neoprene, Polyvinyl chloride.

Explain the difference between Buna-N and Buna-S.

How are polymers classified on the basis of structure?

Define thermoplastics and thermosetting polymers with two examples of each.

Explain the term copolymerisation and give two examples.

Write the monomers used for getting the following polymers. (i) Polyvinyl chloride (ii) Teflon (iii) Bakelite

How do you explain the functionality of a monomer?

Identify the monomer in the following polymeric structures.

(i)

(ii)

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.

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)

(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.

The rate constant for the decomposition of N₂O₅ at various temperatures is given below:

Draw a graph between ln k and 1/T and calculate the values of A and E_a.

Predict the rate constant at 30 º and 50 ºC.

What are the factors which influence the adsorption of a gas on a solid?

Outline the principles of refining of metals by the following methods:

(i) Zone refining

(ii) Electrolytic refining

(iii) Vapour phase refining

p-Dichlorobenzene has higher m.p. and lower solubility than those of o- and m-isomers. Discuss.

Comment on the statement that "colloid is not a substance but a state of substance".

Why is BiH3 the strongest reducing agent amongst all the hydrides of Group 15 elements?

What is meant by unidentate, didentate and ambidentate ligands? Give two examples for each.

Out of C and CO, which is a better reducing agent at 673 K?

Write structures of different dihalogen derivatives of propane.

How the following conversions can be carried out?

(i) Propene to propan-1-ol

(ii) Ethanol to but-1-yne

(iii) 1-Bromopropane to 2-bromopropane

(iv) Toluene to benzyl alcohol

(v) Benzene to 4-bromonitrobenzene

(vi) Benzyl alcohol to 2-phenylethanoic acid

(vii) Ethanol to propanenitrile

(viii) Aniline to chlorobenzene

(ix) 2-Chlorobutane to 3, 4-dimethylhexane

(x) 2-Methyl-1-propene to 2-chloro-2-methylpropane

(xi) Ethyl chloride to propanoic acid

(xii) But-1-ene to n-butyliodide

(xiii) 2-Chloropropane to 1-propanol

(xiv) Isopropyl alcohol to iodoform

(xv) Chlorobenzene to p-nitrophenol

(xvi) 2-Bromopropane to 1-bromopropane

(xvii) Chloroethane to butane

(xviii) Benzene to diphenyl

(xix) tert-Butyl bromide to isobutyl bromide

(xx) Aniline to phenylisocyanide