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Question

Hydrolysis of dimethyldichlorosilane followed by condensation polymerization gives:

A
Monomers
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B
Dimers
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C
Polymers
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D
Trimers
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Solution

The correct option is C Polymers
The silane derivatives on hydrolysis give hydroxides which immediately condense by intramolecular elimination of water, resulting in a polymer chain.
(CH3)2SiCl2+2H2O(CH3)2Si(OH)2
THEORY
Silicones:
  • Synthetic organosilicon compounds having repeated R2SiO units held by Si – O – Si linkages.
  • (R2SiO)n where R = alkyl or aryl group.
  • Silicones can be prepared from the following types of compounds only
  1. R3SiCl
  2. R2SiCl2
  3. RSiCl3
  • Formed by the hydrolysis of alkyl or aryl substituted chlorosilanes and their subsequent polymerisation.
  • CH3Cl reacts with Si in the presence of Cu as a catalyst at a 573K various types of methyl-substituted chlorosilane of formula formed.
  1. MeSiCl3
  2. Me2SiCl2
  3. Me3SiCl
  4. small amount of Me4Si

MeCl+SiCu−−−300 CMeSiCl3+Me2SiCl2+Me3SiCl+traces ofMe4Si
Preparation:

  • Hydrolysis of (CH3)2SiCl2 followed by condensation polymerization yields straight chain polymers.

2CH3Cl+SiCu powder−−−−−570 K(CH3)2SiCl2+2H2O−−−2HCl(CH3)2Si(OH)2

The chain length of the polymer can be controlled by adding (CH3)3SiCl which blocks the ends.


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