Macroer Messages 27 Reaction score 0 Thread starter Apr 20, 2010 #1 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. Attachments polymer.JPG 3.5 KB · Views: 479
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.
chemisttree Science Advisor Homework Helper Gold Member Messages 3,954 Reaction score 777 Apr 21, 2010 #2 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?
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?
Macroer Messages 27 Reaction score 0 Apr 21, 2010 #3 Initiation: I* + CH2=CCl-CH2-CH3--> I-CH2-CHCl*-CH2-CH3How is that for initiation step? where I is initiator and * is radical sign
Initiation: I* + CH2=CCl-CH2-CH3--> I-CH2-CHCl*-CH2-CH3How is that for initiation step? where I is initiator and * is radical sign
chemisttree Science Advisor Homework Helper Gold Member Messages 3,954 Reaction score 777 Apr 22, 2010 #4 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)
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)
Macroer Messages 27 Reaction score 0 Apr 22, 2010 #5 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--> I-CH2-CCl*-CH2-CH3 And i am not sure what the "end groups" you are referring to are.
chemisttree Science Advisor Homework Helper Gold Member Messages 3,954 Reaction score 777 Apr 22, 2010 #6 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* + 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?
Macroer Messages 27 Reaction score 0 Apr 22, 2010 #7 I don't understand where you got the 2nd chlorine atom from
chemisttree Science Advisor Homework Helper Gold Member Messages 3,954 Reaction score 777 Apr 22, 2010 #8 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: Apr 22, 2010
You're right. Should be... (CH3)(I)C-C*(Cl)(CH3) and... The end groups are (CH3)(I)C- in the example above.