Related Questions

Monomer A is reacted with a monomer B in boiling methanol to form a salt. The salt dissolved in water with a little amount of acetic acid is then processed in autoclave at different temperatures and pressure. Monomer A is a bifunctional monomer having amine groups. What is the name of monomer B?
A polymer ‘A’ is formed by the polymerization of monomer B. Monomer B is formed by the pyrolysis of monochlorodifluoromethane in contact with platinum at 700 ᵒC. Monomer is a highly crystalline polymer with excellent insulation properties. What is the name of monomer B?
Which of the following monomer has the least reactivity towards anionic polymerization?
What kind of substituent groups should be attached to the monomer, readily undergoing cationic polymerization?
What is true about the degree of cationic polymerization when termination occurs by monomer transfer?
Which of the following monomer has the highest reactivity towards the styrene radical?
The styrene radical is apparently 500-1000 times less reactive than the vinyl acetate monomer, and also the styrene monomer is 50-100 times less reactive than the vinyl acetate monomer. State true or false.
How does degree of polymerization affected with increase in temperature of cationic polymerization reaction?
How is the rate of polymerization dependent on the concentration of catalyst in cationic polymerization?
What is the range of activation energy of overall polymerization of cationic polymerization?