Concept explainers
(a)
Interpretation:
For the given
(a)
Explanation of Solution
Given polymer structure,
The name of the above polymer is poly(1-butene) because it is formed by the
(b)
Interpretation:
For the given polymer structure, name has to be given.
(b)
Explanation of Solution
Given polymer structure,
The name of the above polymer is poly(ethyl vinyl ether) because it is formed by the polymerization reaction of ethyl vinyl ether.
(c)
Interpretation:
For the given polymer structure, name has to be given.
(c)
Explanation of Solution
Given polymer structure,
The name of the above polymer is poly(vinyl acetate) because it is formed by the polymerization reaction of vinyl acetate.
(d)
Interpretation:
For the given polymer structure, name has to be given.
(d)
Explanation of Solution
Given polymer structure,
The name of the above polymer is poly(perfluoropropylene) because it is formed by the polymerization reaction of perfluoropropylene.
(e)
Interpretation:
For the given polymer structure, name has to be given.
(e)
Explanation of Solution
Given polymer structure,
The name of the above polymer is poly(2,6-dimethylphenylene oxide) because it is formed by the polymerization reaction of 2,6-dimethylphenol.
(f)
Interpretation:
For the given polymer structure, name has to be given.
(f)
Explanation of Solution
Given polymer structure,
The name of the above polymer is poly(1,4-butylene terephthalate) because it is formed by the polymerization reaction of 1,4-butanediol with terephthalic acid.
(g)
Interpretation:
For the given polymer structure, name has to be given.
(g)
Explanation of Solution
Given polymer structure,
The name of the above polymer is poly(3-chloromethylphenylethylene) because it is formed by the polymerization reaction of 3-chloromethylstyrene.
(h)
Interpretation:
For the given polymer structure, name has to be given.
(h)
Explanation of Solution
Given polymer structure,
The name of the above polymer is poly(hexamethylene sebacamide) because it is formed by the polymerization reaction of hexamethylenediamine with sebacoyl chloride.
Want to see more full solutions like this?
Chapter 29 Solutions
Organic Chemistry
- Determine if the following salt is neutral, acidic or basic. If acidic or basic, write the appropriate equilibrium equation for the acid or base that exists when the salt is dissolved in aqueous solution. If neutral, simply write only NR. Be sure to include the proper phases for all species within the reaction LiNO3arrow_forwardAn unknown weak acid with a concentration of 0.410 M has a pH of 5.600. What is the Ka of the weak acid?arrow_forward(racemic) 19.84 Using your reaction roadmaps as a guide, show how to convert 2-oxepanone and ethanol into 1-cyclopentenecarbaldehyde. You must use 2-oxepanone as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way. & + EtOH H 2-Oxepanone 1-Cyclopentenecarbaldehydearrow_forward
- R₂ R₁ R₁ a R Rg Nu R₂ Rg R₁ R R₁₂ R3 R R Nu enolate forming R₁ R B-Alkylated carbonyl species or amines Cyclic B-Ketoester R₁₁ HOB R R₁B R R₁₂ B-Hydroxy carbonyl R diester R2 R3 R₁ RB OR R₂ 0 aB-Unsaturated carbonyl NaOR Aldol HOR reaction 1) LDA 2) R-X 3) H₂O/H₂O ketone, aldehyde 1) 2°-amine 2) acid chloride 3) H₂O'/H₂O 0 O R₁ R₁ R R₁ R₁₂ Alkylated a-carbon R₁ H.C R₁ H.C Alkylated methyl ketone acetoacetic ester B-Ketoester ester R₁ HO R₂ R B-Dicarbonyl HO Alkylated carboxylic acid malonic ester Write the reagents required to bring about each reaction next to the arrows shown. Next, record any regiochemistry or stereochemistry considerations relevant to the reaction. You should also record any key aspects of the mechanism, such as forma- tion of an important intermediate, as a helpful reminder. You may want to keep track of all reactions that make carbon-carbon bonds, because these help you build large molecules from smaller fragments. This especially applies to the reactions in…arrow_forwardProvide the reasonable steps to achieve the following synthesis.arrow_forwardIdentify which compound is more acidic. Justify your choice.arrow_forward
- Provide the reasonable steps to achieve the following synthesis.arrow_forwardWhen anisole is treated with excess bromine, the reaction gives a product which shows two singlets in 1H NMR. Draw the product.arrow_forward(ii) Draw a reasonable mechanism for the following reaction: CI NaOH heat OH (hint: SNAr Reaction) :arrow_forward
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
Living By Chemistry: First Edition TextbookChemistryISBN:9781559539418Author:Angelica StacyPublisher:MAC HIGHER