Determine the functionality of the following monomer CH2 –NH2 | CH₂ || HOOC–CH2–CH2–C–CH2−C=CH, in a reaction that produces ester linkages. in a reaction that produces amide linkages; (i) (ii) (iii) in a free radical addition reaction Give an example of monomer that can be used in each of the above reactions.

Determine the functionality of the following monomer CH2 –NH2 | CH₂ || HOOC–CH2–CH2–C–CH2−C=CH, in a reaction that produces ester linkages. in a reaction that produces amide linkages; (i) (ii) (iii) in a free radical addition reaction Give an example of monomer that can be used in each of the above reactions.

Chemistry: The Molecular Science

5th Edition

ISBN:9781285199047

Author:John W. Moore, Conrad L. Stanitski

Publisher:John W. Moore, Conrad L. Stanitski

Chapter10: Fuels, Organic Chemicals, And Polymers

Section: Chapter Questions

Problem 122QRT

See similar textbooks

Similar questions

Write the line-angle formula for the organic compounds (a) propene; (b) heptan-1-ol;(c) chloroacetic acid; (d) hexanoic acid.
Arrange the following compounds in increasing order of their property as indicated :(i) CH3COCH3, C6H5COCH3, CH3CHO(reactivity towards nucleophilic addition reaction)(ii) Cl—CH2—COOH, F—CH2—COOH, CH3—COOH (acidic character)
This question is about the chemistry of alkenes, which are unsaturated hydrocarbons. (a) State what is meant by the term unsaturated as applied to a hydrocarbon. (1) (b) An organic compound, X, is an unsaturated hydrocarbon with molecular formula CH₂. (i) Draw the displayed formulae and give the names of two molecules with molecular formula C₂H, which are E/Z isomers. (3) Isomer 1 Isomer 2 Name: Name:
Draw structures for the following haloalkanes. (a) 1,2,3-tribromohexane; (b) 2,2,3,3,4-pentachlorohexane;(c) 1,2-dichloro-4-nitrohexane; (d) 1,2-dichloro-3-methoxycyclopentane
Disiamylborane adds only once to alkynes by virtue of its two bulky secondary isoamylgroups. Disiamylborane is prepared by the reaction of BH3 # THF with an alkene.(a) Draw the structural formulas of the reagents and the products in the preparation ofdisiamylborane
(c) Another alkene is propene, C.H. Describe the mechanism for the addition reaction of propene with bromine, Br₂, to form C₂H₂Br₂. In your answer you should include: the name for the type of reaction which occurs • the name of the product the mechanism using curly arrows to show the movement of electron pairs. Type of addition. Name of product... Mechanism
(b) Draw the structural formula for each of the following compounds. Lukiskan formula struktur bagi setiap sebatian berikut. (i) 3-fluoro-2,4,4-trimethylpent-2-ene (ii) ethyl butanoate (ii) 2,4-dichloro-3-methylpentanoic acid
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]
a) True or false: Alkenes undergo addition reactions andaromatic hydrocarbons undergo substitution reactions.(b) Using condensed structural formulas, write the balancedequation for the reaction of 2-pentene with Br2and name the resulting compound. Is this an addition ora substitution reaction? (c) Write a balanced chemicalequation for the reaction of Cl2 with benzene to make paradichlorobenzenein the presence of FeCl3 as a catalyst. Isthis an addition or a substitution reaction?
Give the molecular formula of a hydrocarbon containingsix carbon atoms that is (a) a cyclic alkane, (b) a cyclicalkene, (c) a linear alkyne, (d) an aromatic hydrocarbon.
Chemistry For propene and 2-methylbutene-2, write the reaction schemes for the electrophilic additions: a) with hydrogen bromide; b) hydration; c) hydrogenation; G) oxidation of KMnO4 under mild and harsh conditions. Name the reaction products
Consider the following proposed structures for benzene, each of which is consistent with the molecular formula C6H6. (iv) CH3CCCCCH3 (v) CH2=CHCCH=CH2 When benzene reacts with chlorine to give C6H5Cl, only one isomer of that compound forms. Which of the five proposed structures for benzene are consistent with this observation? When C6H5Cl reacts further with chlorine to give C6H4Cl2, exactly three isomers of the latter compound form. Which of the five proposed structures for benzene are consistent with this observation?