Chapter 15: Q27. (page 570)
Question: Draw the steps of the mechanism that converts vinyl chloride (CH2CHCl) into poly(vinyl chloride).
Short Answer
Answer
Chapter 15: Q27. (page 570)
Question: Draw the steps of the mechanism that converts vinyl chloride (CH2CHCl) into poly(vinyl chloride).
Answer
All the tools & learning materials you need for study success - in one app.
Get started for freeQuestion: When 3,3-dimethylbut-1-ene is treated with HBr alone, the major product is 2-bromo-2,3- dimethylbutane. When the same alkene is treated with HBr and peroxide, the sole product is 1-bromo-3,3-dimethylbutane. Explain these results by referring to the mechanisms.
Questions: Compounds A and B are isomers having molecular formula C5H12. Heating A with Cl2 gives a single product of monohalogenation, whereas heating B under the same conditions forms three constitutional isomers. What are the structures of A and B?
Question: Draw all resonance structures of the radical that results from abstraction of a hydrogen atom from the antioxidant BHA (butylated hydroxy anisole).
Question: Draw the products formed when each alkene is treated with NBS + hv .
a.
b.
c.
Question: As we will learn in Chapter 30, 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 of A.
b. Why does A react faster than styrene (C6H5CH=CH2)in a cationic polymerization?
What do you think about this solution?
We value your feedback to improve our textbook solutions.