Polymerization of 2-Chloro-2-Butene: Solution

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Homework Statement


How would the polymer of 2-chloro-2-butene look when formed by addition polymerization


Homework Equations





The Attempt at a Solution


I have attached my solution. Please tell me if i am right/wrong and why if it is wrong.
 

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What does the initiator end of the molecule look like? How is the process terminated? What does the other end of the molecule look like?
 
Initiation:

I* + CH2=CCl-CH2-CH3--> I-CH2-CHCl*-CH2-CH3How is that for initiation step? where I is initiator and * is radical sign
 
You drew 2-chloro-1-butene. How about the 2-butene version? Do you think you will need to show the end groups in your answer? (I honestly don't know)
 
I* + CH3-CCl=CH-CH3--> I-CH2-CCl*-CH2-CH3

And i am not sure what the "end groups" you are referring to are.
 
I* + CH3-CCl=CH-CH3 --> (CH3)(Cl)(I)C-C*(Cl)(CH3) Step 1 (not a polymer yet)

The end groups are (CH3)(Cl)(I)C- in the example above. It will always be at the end of the new polymer, thus 'end group'. What about the other end?
 
I don't understand where you got the 2nd chlorine atom from
 
You're right. Should be...

(CH3)(I)C-C*(Cl)(CH3)

and...

The end groups are (CH3)(I)C- in the example above.
 
Last edited:

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