ORG CHEM CONNECT CARD
6th Edition
ISBN: 9781264860746
Author: SMITH
Publisher: MCG
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Textbook Question
Chapter 28, Problem 60P
Although chain branching in radical
a. Draw a stepwise mechanism that illustrates which H must be intramolecularly abstracted to form butyl substituents.
b. Suggest a reason why the abstraction of this H is more facile than the abstraction of other H’s.
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Styrene derivatives such as A can be polymerized by way of cationic rather than radical intermediates. Cationic polymerization is an example of electrophilic addition to an alkene involving carbocations.
a.) Draw a short segment of the polymer formed by the polymerization ofA.b.) Why does A react faster than styrene (C6H5CH=CH2) in a cationicpolymerization?
Which of the following molecules can be used as a monomer to generate this polymer?
So the answer's B... im having quite the trouble
understanding where in the polymer the
double bond broke. Could someone explain
and draw in EXTREME details how the
answer's B and not any other answer choice?
Neat hand written explanation
Chapter 28 Solutions
ORG CHEM CONNECT CARD
Ch. 28.1 - Prob. 1PCh. 28.2 - Prob. 2PCh. 28.2 - Prob. 3PCh. 28.2 - Draw the mechanism for the radical polymerization...Ch. 28.2 - Prob. 8PCh. 28.2 - Prob. 9PCh. 28.2 - Prob. 10PCh. 28.3 - Problem 30.12
What polymer is formed by anionic...Ch. 28.5 - Prob. 12PCh. 28.5 - Prob. 13P
Ch. 28.6 - Problem 30.15
What polyamide is formed from each...Ch. 28.6 - Prob. 19PCh. 28.7 - Prob. 20PCh. 28.8 - Prob. 21PCh. 28.9 - Prob. 22PCh. 28.9 - Prob. 23PCh. 28 - Prob. 24PCh. 28 - Prob. 25PCh. 28 - 30.30 Draw each polymer in Problem 30.29 using the...Ch. 28 - Prob. 44PCh. 28 - 30.49 Draw the products of each reaction.
a. e....Ch. 28 - Prob. 56PCh. 28 - 30.56 Compound A is a novel poly (ester amide)...Ch. 28 - 30.57 Researchers at Rutgers University have...Ch. 28 - 30.58 Melmac, a thermosetting polymer formed from...Ch. 28 - 30.59 Although chain branching in radical...Ch. 28 - Prob. 61P
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- 2) For the monomer given determine what type of polymerization (radical, anionic, cationic, and/or step-wise) it will undergo most readily or if it will not undergo polymerization at all. Explain your answer. A.arrow_forward( give typed answer with detail explanation of all part , dont give handwritten )arrow_forward1.- Why are carbon nanotubes and graphene currently considered as reinforcing additives for polymers? What effect do they have on the polymer? What is the mechanism by which they can enhance the Young’s modulus and tensile strength of a polymer? 2.- Kapton is the trade name of a polyimide a) How would you synthesize this polymer? b) During the first stage of the reaction, poly(amic acid) is formed. If you need to follow this stage of the polymerization, what spectroscopic techniques would you use and what groups should you focus on? c) How would you form Kapton films, which can be used as support for solar sails? d) What are the disadvantages of Kapton that have limited their use? Why does this polymer present this weakness?arrow_forward
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