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?

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?

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter29: Organic Polymer Chemistry

Section: Chapter Questions

Problem 29.27P

See similar textbooks

Similar questions

As we will learn in Chapter 28, 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?
1. which cannot be obtained by radical polymerization of its vinyl monomer Poly(ethylene) obtained by polymerization of ethylene monomer Poly(propylene) obtained by polymerization of propylene monomer Poly(vinyl chloride) obtained by polymerization of vinyl chloride monomer Poly(acrylonitrile) obtained by polymerization of acrylonitrile monomer
TOPIC: Preparation of Ethylene Expound and explain the given answer to the question.
6. Dacron is the brand name for the polymer that is made from ethane-1,2-diol and benzene-1,4-dicarboxylic acid. (a) When the two monomers combine, what type of reaction do they undergo and what molecule is eliminated? [1] (b) What is the name for the linkages that join the monomers together? [1] (c) Draw the monomers and the polymer of the reaction to create Dacron. [3]
Markovnikov's rule can best be explained by considering * a) the number of hydrogen atoms attached to each of the double bond carbons atoms. b) the number of alkyl groups attached to each of the double bond carbons atoms. c) the relative stabilities of the carbocations that can be formed from the alkene. d) the spatial arrangement of the groups around the double bond. e) All of the above are good explanations for Markovnikov's rule.
(Organic chemistry) Fill in the missi starting materials or reagents
5.) cyclopentane Why slightly soluble in water? Why insoluble in HCl? Why completely soluble in NaOH? Why insoluble in NaHCO?
5. Which of the following statement(s) is/are correct about (inorganic benzene (1) It contains pr-dn back bond. (2) It does not give addition product with HCl like organic benzene.
1. What is it's type of reaction (Sn1, Sn2, E1, E2, Nucleophilic Addition, Nucleophilic Acyl Substition or Redox reaction). 2.What is it's major product.
C. D. B. 1) Give the major organic product of the following reaction. Don't forget stereochemistry in certain cases. 2) Assign the reaction as addition, elimination, substitution, or rearrangement. A. D D 1. H₂O/Hg(OAC) 2 2. NaBH4 Br₂ CCl4 (inert solvent) H₂/Pd/C HBr Type of Reaction: Type of Reaction: Type of Reaction: Type of Reaction:
When certain cycloalkenes are used in metathesis reactions, ringopening metathesis polymerization (ROMP) occurs to form a highmolecular- weight polymer, as shown with cyclopentene as the starting material. The reaction is driven to completion by relief of strain in the cycloalkene.What products are formed by ring-opening metathesis polymerization of each alkene?
A) An Alcohol X has the structure of (CH,), C(OH)CH(CH,),. i) State the IUPAC name of alcohol X. i) Outline the mechanism for the reaction occurring when alcohol X is converted into 2,3-dimethylbut-2-ene in the presence of a strong acid. i) Name the reaction in part ii). iv) Draw the structure and state the IUPAC name of an isomer of 2,3-dimethyl-2- butene which is also formed in the reaction. v) Explain why two products are obtained. vi) Write an equation for the reaction between alcohol X and ethanoyl chloride. vii) Outline a mechanism for this reaction, using ROH to represent the alcohol in the mechanism.