EBK ORGANIC CHEMISTRY
8th Edition
ISBN: 8220102744127
Author: Bruice
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Question
Chapter 27, Problem 31P
Interpretation Introduction
Interpretation:
A transesterification reaction mechanism that produces dimethyl terephthalate and 1,2-ethanediol from poly(ethylene terephthalate) and methanol has to be shown.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
Provide the mechanism for the step-growth polymerization of citric acid and ethylene glycol to form poly (ethylene glycol)-citrate. Show all steps.
Poly(ethylene terephthalate) is a linear polyester that can be synthesized from the condensation polymerization between terephthalic acid and ethylene glycol, as shown previously in Equation 26-27. What alcohol would you react with terephthalic acid to produce a branched polyester? Draw a portion of the resulting polymer that shows a main chain and one branching point.
Poly(ethylene terephthalate) is a linear polyester that can be synthesized from the condensation polymerization between terephthalic acid and ethylene glycol, as shown previously in Equation 26-27. What alcohol would you react with terephthalic acid to produce a branched polyester? Draw a portion of the resulting polymer that shows a main chain and one branching point.
Chapter 27 Solutions
EBK ORGANIC CHEMISTRY
Ch. 27.3 - Prob. 1PCh. 27.3 - Prob. 2PCh. 27.3 - Prob. 3PCh. 27.3 - Prob. 4PCh. 27.3 - Prob. 5PCh. 27.3 - Prob. 6PCh. 27.4 - Prob. 7PCh. 27.5 - Rank the following groups of monomers from most...Ch. 27.5 - Why does methyl methacrylate not undergo cationic...Ch. 27.6 - Prob. 10P
Ch. 27.6 - Explain why, when propylene oxide undergoes...Ch. 27.6 - Which monomer and which type of initiator can you...Ch. 27.6 - Prob. 13PCh. 27.8 - Draw a short segment of gutta-percha.Ch. 27.8 - Prob. 15PCh. 27.11 - Prob. 16PCh. 27.11 - Write an equation that explains what happens if a...Ch. 27.11 - What happens to polyester slacks if aqueous NaOH...Ch. 27.11 - a. Propose a mechanism for the formation of the...Ch. 27.11 - Explain why, when a small amount of glycerol is...Ch. 27.12 - Propose a mechanism for the formation of melmac.Ch. 27.12 - Prob. 22PCh. 27.13 - Prob. 23PCh. 27 - Draw short segments of the polymers obtained from...Ch. 27 - Prob. 25PCh. 27 - Prob. 26PCh. 27 - Draw the structure of the monomer or monomers used...Ch. 27 - Prob. 28PCh. 27 - Draw short segments of the polymers obtained from...Ch. 27 - Quiana is a synthetic fabric that feels very much...Ch. 27 - Prob. 31PCh. 27 - Prob. 32PCh. 27 - Prob. 33PCh. 27 - Poly(vinyl alcohol) is a polymer used to make...Ch. 27 - Five different repeating units are found in the...Ch. 27 - Prob. 37PCh. 27 - A particularly strong and rigid polyester used for...Ch. 27 - Prob. 39PCh. 27 - Which Monomer gives a greater yield of polymer,...Ch. 27 - Prob. 41PCh. 27 - Prob. 42PCh. 27 - Why do vinyl raincoats become brittle as they get...Ch. 27 - The polymer shown below is synthesized by...Ch. 27 - Prob. 45PCh. 27 - How can head-to-head poly(vinyl bromide) be...Ch. 27 - Delrin (polyoxymethylene) is a tough...
Knowledge Booster
Similar questions
- Draw the repeat unit of the polymer produced by cationic polymerization of 1,3-dioxolane using HBF4, a strong acid, as catalyst. 1,3-dioxolanearrow_forwardPoly(vinyl alcohol), a hydrophilic polymer used in aqueous adhesives, is made by polymerizing vinyl acetate and then hydrolyzing the ester linkages. We have seen that basic hydrolysis destroys the Dacron polymer. Poly(vinyl acetate) is converted to poly(vinyl alcohol) by a basic hydrolysis of the ester groups. Why doesn’t the hydrolysis destroy the poly(vinyl alcohol)polymer?arrow_forwardDraw the structure of the following polymers and indicate the polymerization type responsible for the givenpolymers.Indicate, where appropriate, the polyester, polyamide or polyurethane linkages.a) Poly(ethene terephthalate)b) Poly(vinyl alcohol)c) Polyisoprene and isomer structures of polyisoprened) Poly(methyl methacrylate)e) Polycaprolactamarrow_forward
- Poly(trimethylene carbamate) is used in high-quality synthetic leather.Draw the products that would be formed if the polymer were completelyhydrolyzed under acidic or basic conditions.arrow_forwardDraw the structure of the polymer formed from ring-opening metathesis polymerization (ROMP) of each monomer.arrow_forwardKodel is a condensation polymer made from terephthalic acid and 1,4-cyclohexanedimethanol. Write the structure of the resulting polymer.arrow_forward
- Poly(vinyl alcohol), a hydrophilic polymer used in aqueous adhesives, is made by polymerizing vinyl acetate and then hydrolyzing the ester linkages. Why is poly(vinyl alcohol) made by this circuitous route? Why not just polymerize vinyl alcohol?arrow_forwardDraw a structural formula of the polymer resulting from base-catalyzed polymerization of each compound. Would you expect the polymers to be optically active? (S)-(+)-lactide is the dilactone formed from two molecules of (S)-(+)-lactic acid.arrow_forwardShow the differences between the chain-growth and step-growth mechanisms of polymerization.arrow_forward
- Show the mechanism for the transesterification reaction that recycles poly(ethylene terephthalate) to dimethyl terephthalate and 1,2-ethanediol when the polymer is heated in an acidic solution of methanol.arrow_forwardPTT (polytrimethylene terephthalate) is a polyester formed from 1,3-propanediol (HOCH 2CH 2CH 2OH) by the given reaction. PTT is sold under the trade name Sorona by DuPont. 1,3-Propanediol can now be made from a plant source like corn, rather than from petroleum starting materials. This makes PTT a more environmentally friendly polyester than PET. What is the structure of PTT?arrow_forward1. Please write the repeating unit of product and byproduct from condensation polymerization. n HO-CH2CH2CH2CH2OH + In HO-C -OH HO. چہ HO SA + EG OH d'a ONa ONa HO " 1,4-benzenedicarboxylic acid OH " H₂N 1,4-benzenediamine NH2arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- EBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENTOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning