CHEMICAL PRINCIPLES PKG W/SAPLING
7th Edition
ISBN: 9781319086411
Author: ATKINS
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 11, Problem 11D.31E
(a)
Interpretation Introduction
Interpretation:
The type of reaction of 1-butene with chlorine in the absence of light has to be given.
(b)
Interpretation Introduction
Interpretation:
The type of reaction of
Concept Introduction:
Refer to part (a).
(c)
Interpretation Introduction
Interpretation:
The type of reaction of hydrogenation of 1-butyne has to be given.
Concept Introduction:
Refer to part (a).
(d)
Interpretation Introduction
Interpretation:
The type of reaction of polymerization of styrene has to be given.
Concept Introduction:
Refer to part (a).
(e)
Interpretation Introduction
Interpretation:
The type of reaction of methylamine with butanoic acid has to be given.
Concept Introduction:
Refer to part (a).
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Draw the organic product formed when the following compounds undergo a substitution reaction: (a) acetic acid and 1-hexanol; (b) propanoic acid and dimethyl-amine; (c) ethanoic acid and diethylamine.
Draw the organic product formed when the following compounds undergo a substitution reaction: (a) acetic acid and methyl-amine; (b) butanoic acid and 2-propanol; (c) Formica acid and 2-methyl-1-propanol.
A polymer closely related to PET is PBT, which is made from terephthalic acid and butane-1,4-diol.(a) Propose a structure for PBT and write the condensed formula for the structure.(b) What does PBT stand for? That is, what do you expect the trivial name of PBT to be?(c) Would you expect PBT to have a higher or lower melting point than PET? Justify your answer.(d) PBT, rather than PET, is used in molding because it crystallizes faster. Explain why PBT crystallizes more quickly than PET.
Chapter 11 Solutions
CHEMICAL PRINCIPLES PKG W/SAPLING
Ch. 11 - Prob. 11A.1ASTCh. 11 - Prob. 11A.1BSTCh. 11 - Prob. 11A.2ASTCh. 11 - Prob. 11A.2BSTCh. 11 - Prob. 11A.3ASTCh. 11 - Prob. 11A.3BSTCh. 11 - Prob. 11A.4ASTCh. 11 - Prob. 11A.4BSTCh. 11 - Prob. 11A.5ASTCh. 11 - Prob. 11A.5BST
Ch. 11 - Prob. 11A.6ASTCh. 11 - Prob. 11A.6BSTCh. 11 - Prob. 11A.1ECh. 11 - Prob. 11A.2ECh. 11 - Prob. 11A.3ECh. 11 - Prob. 11A.4ECh. 11 - Prob. 11A.5ECh. 11 - Prob. 11A.6ECh. 11 - Prob. 11A.7ECh. 11 - Prob. 11A.8ECh. 11 - Prob. 11A.9ECh. 11 - Prob. 11A.10ECh. 11 - Prob. 11A.11ECh. 11 - Prob. 11A.12ECh. 11 - Prob. 11A.13ECh. 11 - Prob. 11A.14ECh. 11 - Prob. 11A.15ECh. 11 - Prob. 11A.16ECh. 11 - Prob. 11A.17ECh. 11 - Prob. 11A.18ECh. 11 - Prob. 11A.19ECh. 11 - Prob. 11A.20ECh. 11 - Prob. 11A.21ECh. 11 - Prob. 11A.22ECh. 11 - Prob. 11A.23ECh. 11 - Prob. 11A.24ECh. 11 - Prob. 11A.25ECh. 11 - Prob. 11A.26ECh. 11 - Prob. 11A.27ECh. 11 - Prob. 11A.28ECh. 11 - Prob. 11B.1ASTCh. 11 - Prob. 11B.1BSTCh. 11 - Prob. 11B.1ECh. 11 - Prob. 11B.3ECh. 11 - Prob. 11B.4ECh. 11 - Prob. 11B.5ECh. 11 - Prob. 11B.6ECh. 11 - Prob. 11B.7ECh. 11 - Prob. 11B.8ECh. 11 - Prob. 11C.1ASTCh. 11 - Prob. 11C.1BSTCh. 11 - Prob. 11C.1ECh. 11 - Prob. 11C.2ECh. 11 - Prob. 11C.3ECh. 11 - Prob. 11C.4ECh. 11 - Prob. 11C.5ECh. 11 - Prob. 11C.6ECh. 11 - Prob. 11C.7ECh. 11 - Prob. 11C.8ECh. 11 - Prob. 11C.9ECh. 11 - Prob. 11C.10ECh. 11 - Prob. 11C.11ECh. 11 - Prob. 11C.12ECh. 11 - Prob. 11C.13ECh. 11 - Prob. 11C.14ECh. 11 - Prob. 11D.1ASTCh. 11 - Prob. 11D.1BSTCh. 11 - Prob. 11D.2ASTCh. 11 - Prob. 11D.2BSTCh. 11 - Prob. 11D.3ASTCh. 11 - Prob. 11D.3BSTCh. 11 - Prob. 11D.1ECh. 11 - Prob. 11D.2ECh. 11 - Prob. 11D.3ECh. 11 - Prob. 11D.4ECh. 11 - Prob. 11D.5ECh. 11 - Prob. 11D.6ECh. 11 - Prob. 11D.7ECh. 11 - Prob. 11D.8ECh. 11 - Prob. 11D.9ECh. 11 - Prob. 11D.10ECh. 11 - Prob. 11D.11ECh. 11 - Prob. 11D.12ECh. 11 - Prob. 11D.13ECh. 11 - Prob. 11D.14ECh. 11 - Prob. 11D.15ECh. 11 - Prob. 11D.16ECh. 11 - Prob. 11D.17ECh. 11 - Prob. 11D.18ECh. 11 - Prob. 11D.19ECh. 11 - Prob. 11D.20ECh. 11 - Prob. 11D.21ECh. 11 - Prob. 11D.22ECh. 11 - Prob. 11D.23ECh. 11 - Prob. 11D.24ECh. 11 - Prob. 11D.25ECh. 11 - Prob. 11D.26ECh. 11 - Prob. 11D.27ECh. 11 - Prob. 11D.28ECh. 11 - Prob. 11D.29ECh. 11 - Prob. 11D.30ECh. 11 - Prob. 11D.31ECh. 11 - Prob. 11D.32ECh. 11 - Prob. 11D.33ECh. 11 - Prob. 11D.34ECh. 11 - Prob. 11D.35ECh. 11 - Prob. 11D.36ECh. 11 - Prob. 11E.1ASTCh. 11 - Prob. 11E.1BSTCh. 11 - Prob. 11E.2ASTCh. 11 - Prob. 11E.2BSTCh. 11 - Prob. 11E.1ECh. 11 - Prob. 11E.3ECh. 11 - Prob. 11E.4ECh. 11 - Prob. 11E.5ECh. 11 - Prob. 11E.7ECh. 11 - Prob. 11E.8ECh. 11 - Prob. 11E.9ECh. 11 - Prob. 11E.10ECh. 11 - Prob. 11E.11ECh. 11 - Prob. 11E.12ECh. 11 - Prob. 11E.13ECh. 11 - Prob. 11E.14ECh. 11 - Prob. 11E.15ECh. 11 - Prob. 11E.16ECh. 11 - Prob. 11E.17ECh. 11 - Prob. 11E.18ECh. 11 - Prob. 11E.19ECh. 11 - Prob. 11E.20ECh. 11 - Prob. 11E.21ECh. 11 - Prob. 11E.22ECh. 11 - Prob. 11E.23ECh. 11 - Prob. 11E.24ECh. 11 - Prob. 11E.25ECh. 11 - Prob. 11E.26ECh. 11 - Prob. 11E.27ECh. 11 - Prob. 11E.28ECh. 11 - Prob. 11.1ECh. 11 - Prob. 11.2ECh. 11 - Prob. 11.3ECh. 11 - Prob. 11.4ECh. 11 - Prob. 11.5ECh. 11 - Prob. 11.6ECh. 11 - Prob. 11.7ECh. 11 - Prob. 11.8ECh. 11 - Prob. 11.9ECh. 11 - Prob. 11.10ECh. 11 - Prob. 11.11ECh. 11 - Prob. 11.12ECh. 11 - Prob. 11.13ECh. 11 - Prob. 11.14ECh. 11 - Prob. 11.15ECh. 11 - Prob. 11.16ECh. 11 - Prob. 11.17ECh. 11 - Prob. 11.18ECh. 11 - Prob. 11.19ECh. 11 - Prob. 11.20ECh. 11 - Prob. 11.21ECh. 11 - Prob. 11.23ECh. 11 - Prob. 11.24ECh. 11 - Prob. 11.25ECh. 11 - Prob. 11.26ECh. 11 - Prob. 11.27ECh. 11 - Prob. 11.28ECh. 11 - Prob. 11.29ECh. 11 - Prob. 11.30ECh. 11 - Prob. 11.31ECh. 11 - Prob. 11.32ECh. 11 - Prob. 11.33ECh. 11 - Prob. 11.34ECh. 11 - Prob. 11.35ECh. 11 - Prob. 11.36ECh. 11 - Prob. 11.37ECh. 11 - Prob. 11.38ECh. 11 - Prob. 11.41ECh. 11 - Prob. 11.42ECh. 11 - Prob. 11.43ECh. 11 - Prob. 11.44ECh. 11 - Prob. 11.45ECh. 11 - Prob. 11.47ECh. 11 - Prob. 11.49ECh. 11 - Prob. 11.50ECh. 11 - Prob. 11.51ECh. 11 - Prob. 11.52ECh. 11 - Prob. 11.53ECh. 11 - Prob. 11.54ECh. 11 - Prob. 11.55ECh. 11 - Prob. 11.56ECh. 11 - Prob. 11.57E
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- (1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3.4-Dimethylcyclodecyne with sodium amidearrow_forwarda) 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?arrow_forward3. Dacron is the brand name for the polymer that is made from ethane-1,2-diol and benzene-1,4-dicarboxylic acid. (a) What type of polymer is Dacron? (b) When the two monomers combine, what type of reaction do they undergo and what molecule is eliminated? (c) What is the name for the linkages that join the monomers together?(d) Draw the monomers and the polymer of the reaction to create Dacron. (Use a condensed structural formula in your answer.) HC-C styrene H-O-C- ethane-1,2-diol I H OH НО. 206 H -C-0-H H benzene-1.4-dicarboxylic acid.arrow_forward
- Draw the product resulting from mild oxidation of (a) 2-butanol; (b) 2-methylpropanal; (c) cyclopentanol.arrow_forwardWrite the chemical reaction showing the formation of the following polymers from initial reactants: (a) nylon, (b) lexan, (c) terylene, (d) polyurethane.arrow_forwardPropene and benzene react with bromine, Br2, in absence of UV light in different ways. The reaction of propene is an addition reaction whereas that of benzene is a substitution reaction. Give the best explanation of this difference.arrow_forward
- Which chemical formulas represent organic compounds and which represent inorganic compounds: (a) H 2SO 4; (b) Br 2; (c) C 5H 12?arrow_forward5. Give the structural formulae and name the functional groups of the following compounds. (a) 3-chlorobut-1-ene (b) butanedioic acid Name the functional group: (c) propanamide Name the functional group: (d) 3-methylbutanal Name the functional group: Name the functional group:arrow_forwardWrite the polymerization reaction in which acetylene (C2H2) produces polyacetylene. Show the structural formulae of the monomers and the polymer.arrow_forward
- Write an equation for the formation of the following polymers.(a) Polystyrene, from styrene (C6H5CH=CH2)(b) PET (polyethylene terephthalate), from ethylene glycol and terephthalic acidarrow_forwardWrite equations for the following: (a) a substitution reac-tion between 2-bromopropane and KI; (b) an addition reactionbetween cyclohexene and Cl2; (c) an addition reaction between2-propanone and H2(Ni metal is a catalyst)arrow_forwardWrite equations for the following: (a) an addition reactionbetween H₂O and 3-hexene (H⁺ is a catalyst); (b) an eliminationreaction between 2-bromopropane and hot potassium ethoxide,CH₃—CH₂—OK (KBr and ethanol are also products); (c) alight-induced substitution reaction between Cl₂ and ethane toform 1,1-dichloroethane.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher: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 Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
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