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What is the mechanism of the polymerization reaction for the synthesis of polyvinyl alcohol from vinyl acetate monomer?

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The synthesis of polyvinyl alcohol  PVA  from vinyl acetate monomer  VAM  involves two main steps: the polymerization of vinyl acetate to form polyvinyl acetate  PVAc  and the hydrolysis of polyvinyl acetate to form polyvinyl alcohol.1. Polymerization of vinyl acetate to polyvinyl acetate:The polymerization of vinyl acetate is typically carried out through a free radical mechanism. This process can be initiated by heat, light, or chemical initiators, such as peroxides or azo compounds. The mechanism involves the following steps:a. Initiation: The initiator generates free radicals, which react with the vinyl acetate monomer to form a primary radical.Initiator  2 RR + CH2=CHOAc  R-CH2-CHOAcb. Propagation: The primary radical reacts with another vinyl acetate monomer, forming a new radical. This process continues, leading to the growth of the polymer chain.R-CH2-CHOAc + CH2=CHOAc  R-CH2-CHOAc-CH2-CHOAcc. Termination: The polymerization reaction is terminated when two radicals react with each other, forming a stable covalent bond.R-CH2-CHOAc + CHOAc-CH2-R  R-CH2-CHOAc-CHOAc-CH2-RThe result of this polymerization process is polyvinyl acetate  PVAc .2. Hydrolysis of polyvinyl acetate to polyvinyl alcohol:The conversion of polyvinyl acetate to polyvinyl alcohol is achieved through a hydrolysis reaction, which can be either acidic or basic. The mechanism involves the cleavage of the acetate group  OAc  and the formation of a hydroxyl group  OH  in its place.a. Acid-catalyzed hydrolysis:In the presence of an acid catalyst, the carbonyl group of the acetate is protonated, making it more susceptible to nucleophilic attack by water.R-CH2-C =O OAc + H+  R-CH2-C =O OH+OAcWater then attacks the carbonyl carbon, and the acetate group is eliminated as a leaving group.R-CH2-C =O OH+OAc + H2O  R-CH2-C OH2  OH OAc  R-CH2-C OH  OH  + OAc-b. Base-catalyzed hydrolysis:In the presence of a base, the hydroxide ion acts as a nucleophile, attacking the carbonyl carbon of the acetate group.R-CH2-C =O OAc + OH-  R-CH2-C OH  O- OAcThe acetate group is then eliminated as a leaving group, and a proton is transferred to the oxygen atom.R-CH2-C OH  O- OAc  R-CH2-C OH  OH  + OAc-The final product of this hydrolysis reaction is polyvinyl alcohol  PVA .

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