Chemistry: The Central Science (13th Edition)
13th Edition
ISBN: 9780321910417
Author: Theodore E. Brown, H. Eugene LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward, Matthew E. Stoltzfus
Publisher: PEARSON
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Chapter 4.4, Problem 4.8.1PE
(a)
Interpretation Introduction
To determine: The difference between chlorofluorocarbons and hydrofluorocarbons.
(b)
Interpretation Introduction
To determine: The reason for the less harmful nature of hydrofluorocarbons to the ozone layer as compared to CFCs.
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20.21 Predict the major product formed by 1,4-addition of HCI to cyclopentadiene.
20.22 Draw structural formulas for the two constitutional isomers with the molecular for-
mula C₂H,Br, formed by adding one mole of Br, to cyclopentadiene.
Add substituents to draw the conformer below (sighting down the
indicated bond), then rotate the back carbon to provide the conformation
that will be capable of an E2 elimination. R/S stereochemistry is graded.
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OCH 3
Drawing
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and Rings
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20.17 Predict the structure of the major product formed by 1,2-addition of HBr to
3-methylenecyclohexene.
3-Methylenecyclohexene
20.18 Predict the major product formed by 1,4-addition of HBr to 3-methylenecyclohexene.
Chapter 4 Solutions
Chemistry: The Central Science (13th Edition)
Ch. 4.1 - Prob. 4.1.1PECh. 4.1 - How are the boundaries between the regions of the...Ch. 4.2 - Air pollution in the Mexico City metropolitan area...Ch. 4.2 - Prob. 4.2.2PECh. 4.2 - Prob. 4.3.1PECh. 4.2 - Prob. 4.3.2PECh. 4.2 - Prob. 4.4.1PECh. 4.2 - Prob. 4.4.2PECh. 4.3 - Distinguish between photodissociation and...Ch. 4.3 - Prob. 4.5.2PE
Ch. 4.3 - Prob. 4.6.1PECh. 4.3 - Prob. 4.6.2PECh. 4.3 - Do the reactions involved in ozone depletion...Ch. 4.3 - Prob. 4.7.2PECh. 4.4 - Prob. 4.8.1PECh. 4.4 - Prob. 4.8.2PECh. 4.4 - Prob. 4.9.1PECh. 4.4 - Prob. 4.9.2PECh. 4.4 - Prob. 4.10.1PECh. 4.4 - Prob. 4.10.2PECh. 4.5 - Practice Exercise 2 The bond energy in N2 is 941...Ch. 4.5 - Prob. 4.11.2PECh. 4.5 - Prob. 4.12.1PECh. 4.5 - Prob. 4.12.2PECh. 4.5 - Prob. 4.13.1PECh. 4.5 - Prob. 4.13.2PECh. 4.5 - The figure shows the three lowest regions of...Ch. 4.5 - Prob. 4.14.2PECh. 4.6 - Where does the energy come from to evaporate the...Ch. 4.6 - Prob. 4.15.2PECh. 4.6 - Prob. 4.16.1PECh. 4.6 - The first stage of treatment at the reverse...Ch. 4.6 - Prob. 4.17.1PECh. 4.6 - Prob. 4.17.2PECh. 4 - Prob. 1DECh. 4 - Prob. 1ECh. 4 - Prob. 2ECh. 4 - Prob. 3ECh. 4 - Prob. 4ECh. 4 - Prob. 5ECh. 4 - Prob. 6ECh. 4 - Which of the following ions will always be a...Ch. 4 - Prob. 8ECh. 4 - Prob. 9ECh. 4 - Prob. 10ECh. 4 - Prob. 11ECh. 4 - List the common products formed when an organic...Ch. 4 - Prob. 13ECh. 4 - Prob. 14ECh. 4 - Prob. 15ECh. 4 - Prob. 16ECh. 4 - Prob. 17ECh. 4 - Prob. 18ECh. 4 - Prob. 19ECh. 4 - Prob. 20ECh. 4 - Prob. 21ECh. 4 - Prob. 22ECh. 4 - Prob. 23ECh. 4 - Prob. 24ECh. 4 - Prob. 25ECh. 4 - Prob. 26ECh. 4 - Prob. 27ECh. 4 - Prob. 28ECh. 4 - Prob. 29ECh. 4 - Explain, using Le Châtelier’s principle, why the...Ch. 4 - Prob. 31ECh. 4 - Prob. 32ECh. 4 - Prob. 33ECh. 4 - Prob. 34ECh. 4 - Prob. 35ECh. 4 - Prob. 36ECh. 4 - Prob. 37ECh. 4 - Prob. 38ECh. 4 - Prob. 39ECh. 4 - Prob. 40ECh. 4 - Prob. 41ECh. 4 - Prob. 42ECh. 4 - Prob. 43ECh. 4 - Prob. 44ECh. 4 - Prob. 45ECh. 4 - 18.85 The main reason that distillation is a...Ch. 4 - Prob. 47ECh. 4 - Prob. 48ECh. 4 - Prob. 49ECh. 4 - Prob. 50ECh. 4 - Prob. 51ECh. 4 - Prob. 52ECh. 4 - The process of iron being oxidized to make iron...Ch. 4 - At 1 atm pressure, CO2(s) sublimes at 78oC. Is...Ch. 4 - Prob. 55ECh. 4 - Prob. 56ECh. 4 - Prob. 57ECh. 4 - Prob. 58ECh. 4 - Prob. 59ECh. 4 - Prob. 60ECh. 4 - Using the standard molar entropies in Appendix C,...Ch. 4 - Which of these statements is true? All spontaneous...Ch. 4 - Prob. 63ECh. 4 - Prob. 64ECh. 4 - Prob. 65ECh. 4 - Prob. 66ECh. 4 - Prob. 67ECh. 4 - What is the temperature above which the Haber...Ch. 4 - Prob. 69ECh. 4 - Prob. 70ECh. 4 - Prob. 71ECh. 4 - Prob. 72ECh. 4 - Prob. 73ECh. 4 - Prob. 74ECh. 4 - Prob. 75ECh. 4 - Prob. 76ECh. 4 - As shown here, one type of computer keyboard...Ch. 4 - 19.3
a. What are the signs of ΔS and ΔH for the...Ch. 4 - Predict the signs of H and S for this reaction....Ch. 4 - Prob. 80ECh. 4 - The accompanying diagram shows how H (red line)...Ch. 4 - Prob. 82ECh. 4 - Prob. 83ECh. 4 - Prob. 84ECh. 4 - Prob. 85ECh. 4 - Prob. 86ECh. 4 - Prob. 87ECh. 4 - Can endothermic chemical reaction be spontaneous?...Ch. 4 - Prob. 89ECh. 4 - Prob. 90ECh. 4 - Prob. 91AECh. 4 - Prob. 92AECh. 4 - Prob. 93AECh. 4 - Prob. 94AECh. 4 - Prob. 95AECh. 4 - Prob. 96AECh. 4 - Prob. 97AECh. 4 - Prob. 98AECh. 4 - Prob. 99AECh. 4 - Prob. 100AECh. 4 - Prob. 101AECh. 4 - Prob. 102AECh. 4 - Prob. 103AECh. 4 - Alcohol-based fuels for automobiles lead to the...Ch. 4 - Prob. 105IECh. 4 - Prob. 106IECh. 4 - Prob. 107IECh. 4 - Prob. 108IECh. 4 - Prob. 109IECh. 4 - Prob. 110IECh. 4 - Prob. 111IECh. 4 - Prob. 112IECh. 4 - Although there are many ions in seawater, the...Ch. 4 - The Ogallala aquifer described in the Close Look...Ch. 4 - Prob. 115IE
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- + Draw a vicinal alkyl bromide that would produce the following alkene in an E2 elimination. Use a dash or wedge bond to indicate stereochemistry on asymmetric centers, where applicable. Ignore any inorganic byproducts. Br Drawing Strong Base H Q Atoms, Bonds Charges and Rings Draw or tap a new bond to see suggestions. Remove Done 語 Reset Undo + Drag To Panarrow_forwardDraw a vicinal alkyl bromide that would produce the following alkene in an E2 elimination. Use a dash or wedge bond to indicate stereochemistry on asymmetric centers, where applicable. Ignore any inorganic byproducts. + Drawing Į Strong Base H Br Q Atoms, Bonds and Rings Charges Draw or tap a new bond to see suggestions. Undo Reset 謂 Remove Done Drag To Pan +arrow_forwardDraw the product of the E2 reaction shown below. Include the correct stereochemistry. Ignore any inorganic byproducts. + Br CH3 Q Strong Base Drawing Atoms, Bonds and Rings Charges Undo Reset H "Br H N Br. Remove Done .N. Drag To Panarrow_forward
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the product of this elementary step in an elimination mechanism. Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore byproducts. + Br: .. 8 0.01 M NaOH heat Drawing Q Atoms, Bonds and Rings Charges and Lone Pairs Draw or tap a new bond to see suggestions. Undo Reset Remove Done + Drag To Panarrow_forward+ Draw the product of the E2 reaction shown below. Include the correct stereochemistry. Ignore any inorganic byproducts. Ph CH2CH3 H H3C H Br DBN [૪] Drawing Atoms, Bonds and Rings H | OH Charges ―00 H. C | Undo Reset Br I Remove Done Drag To Pan +arrow_forwardReaction A Now the production A Œ In the product of reaction i 12 Dear the product of actionarrow_forward
- Macmillan Learnin When an unknown amine reacts with an unknown acid chloride, an amide with a molecular mass of 163 g/mol (M* = 163 m/z) is formed. In the infrared spectrum, important absorptions appear at 1661, 750 and 690 cm-1. The 13C NMR and DEPT spectra are provided. Draw the structure of the product as the resonance contributor lacking any formal charges. 13C NMR DEPT 90 200 160 120 80 40 0 200 160 120 80 DEPT 135 200 160 120 80 40 0 Draw the unknown amide. 40 40 0arrow_forwardDraw the major product karmed when I reach with the epoxide. Use walge dah bonds, including hydrogen al alcach genic center, to show the chemistry of the product Beeldraw any hydrogen akams on coxygen where applicablearrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. H I Select to Add Arrows + H H 'H Q H2O H2O CI:O .H H H H I Select to Add Arrows I : C H2O H H H Select to Add Arrows 'Harrow_forward
- + Draw an alkyl halide that produces ONLY the following alkene in an E2 elimination. Ignore any inorganic byproducts. Drawing Strong Base Q Atoms, Bonds and Rings Charges HO Br H2N Undo Reset Remove Done Drag To Panarrow_forwardFor the dehydrohalogenation (E2) reaction shown, draw the major organic product. Хок Br tert-butanol heat Select Drew Templates More Erase CH QQQarrow_forwardMacmillan Learning Draw the major, neutral organic product for each substitution reaction. For this question, assume that each substitution reaction goes to completion. Disregard elimination. Reaction A. CI H₂O Select Draw Templates More Erase C Harrow_forward
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