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Arrange the following monomers in order of decreasing ability to undergo cationic polymerisation.

I. CH2=CH -C6H4(NO2)

II. CH2=CH -C6H4(CH3)

III.  CH2=CH -C6H4(OCH3)

(a) I > II > III

(b) II > I > III

(c) III > II > I

(d) I > III > II

1 Answer

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Best answer

The correct option is: (c) III > II > I

Explanation:

Electron releasing groups such as -CH3, -OCH3 activate the monomer towards cationic polymerisation because these groups provide stability to the carbocation formed. On the other hand, -NO2 is a electron withdrawing group. So, it reduces the stability of carbocation formed. Thus, the correct order is

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