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Question

Q.Write the structures of monomers used to obtain the following polymers:

(a) Neoprene
(b) PHBV
(c) Bakelite
(OR)
(a) Arrange the following polymers in decreasing order of their intermolecular forces: Bakelite, Polythene, Buna-S, Nylon-6,6
(b) Write the monomers of the following polymer: −[O−CH2−CH2−O−CO−C6H4−CO]n−-[O-CH_2-CH_2-O-CO-C_6H_4-CO]_n- (a polyester in which a benzene ring, C6H4C_6H_4, links the two −CO−-CO- carbonyl groups).
(c) What is the structural difference between high density polythene (HDP) and low density polythene (LDP)?
CBSECBSE Class XII Board 2019Subjective· 3mImportance★★★★★est
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Part (a): Neoprene → chloroprene; PHBV → 3-hydroxybutanoic + 3-hydroxypentanoic acids; Bakelite → phenol + formaldehyde.

Part (b): (i) Bakelite > Nylon-6,6 > Buna-S > Polythene; (ii) ethylene glycol + terephthalic acid; (iii) HDP = linear, closely packed; LDP = branched, loosely packed.


Monomer structures

(i) Neoprene

A synthetic rubber made by addition (1,4-) polymerisation of chloroprene (2-chlorobuta-1,3-diene):

CH2=C(Cl)−CH=CH2\text{CH}_2=\text{C(Cl)}-\text{CH}=\text{CH}_2

(ii) PHBV

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) is a biodegradable copolyester of two 3-hydroxy acids:

  • 3-hydroxybutanoic acid: CH3−CH(OH)−CH2−COOH\text{CH}_3-\text{CH(OH)}-\text{CH}_2-\text{COOH}
  • 3-hydroxypentanoic acid (3-hydroxyvaleric acid): CH3−CH2−CH(OH)−CH2−COOH\text{CH}_3-\text{CH}_2-\text{CH(OH)}-\text{CH}_2-\text{COOH}

They condense (ester linkages, loss of water) to give the polymer.

(iii) Bakelite

A thermosetting phenol–formaldehyde resin obtained by condensation of:

  • Phenol: C6H5OH\text{C}_6\text{H}_5\text{OH}
  • Formaldehyde: HCHO\text{HCHO}

Formaldehyde bridges the ortho/para positions of phenol as −CH2−-\text{CH}_2- links; on heating a cross-linked 3-D network forms.


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