
Chemical Principles
8th Edition
ISBN: 9781305581982
Author: Steven S. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Question
Chapter 7, Problem 11DQ
Interpretation Introduction
Interpretation: The relationship between
Concept Introduction: An acid is the substance that gives H+ or
On the contrary, a base ionized to given
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Consider the following nucleophilic substitution reaction. The compound listed above the arrow is the solvent for the reaction. If nothing is listed over the arrow,
then the nucleophile is also the solvent for the reaction.
Part 1 of 2
Br
CH,CN
+ I¯
What is the correct mechanism for the reaction? Select the single best answer.
@SN2
○ SN 1
Part: 1/2
Part 2 of 2
Draw the products for the reaction. Include both the major organic product and the inorganic product. If more than one stereoisomer is possible, draw
only one stereoisomer. Include stereochemistry where relevant.
Click and drag to start drawing a
structure.
X
હૈ
20.33 Think-Pair-Share
(a) Rank the following dienes and dienophiles in order of increasing reactivity in the
Diels-Alder reaction.
(i)
CO₂Et
(ii)
COEt
||
CO₂Et
MeO
MeO
(b) Draw the product that results from the most reactive diene and most reactive
dienophile shown in part (a).
(c) Draw a depiction of the orbital overlap involved in the pericyclic reaction that oc-
curs between the diene and dienophile in part (b).
(d) Is the major product formed in part (b) the endo or exo configuration? Explain
your reasoning.
20.40 The following compound undergoes an intramolecular Diels-Alder reaction to give a
tricyclic product. Propose a structural formula for the product.
CN
heat
An intramolecular
Diels-Alder adduct
Chapter 7 Solutions
Chemical Principles
Ch. 7 - Prob. 1DQCh. 7 - Differentiate between the terms strength and...Ch. 7 - Prob. 3DQCh. 7 - Prob. 4DQCh. 7 - Prob. 5DQCh. 7 - Prob. 6DQCh. 7 - Prob. 7DQCh. 7 - Prob. 8DQCh. 7 - Prob. 9DQCh. 7 - Prob. 10DQ
Ch. 7 - Prob. 11DQCh. 7 - Prob. 12DQCh. 7 - Prob. 13DQCh. 7 - Prob. 14DQCh. 7 - Prob. 15DQCh. 7 - Prob. 16DQCh. 7 - Prob. 17DQCh. 7 - Consider the autoionization of liquid ammonia:...Ch. 7 - The following are representations of acidbase...Ch. 7 - Prob. 20ECh. 7 - For each of the following aqueous reactions,...Ch. 7 - Write balanced equations that describe the...Ch. 7 - Write the dissociation reaction and the...Ch. 7 - Prob. 24ECh. 7 - Consider the following illustrations: Which beaker...Ch. 7 - Prob. 26ECh. 7 - Prob. 27ECh. 7 - Prob. 28ECh. 7 - Prob. 29ECh. 7 - Prob. 30ECh. 7 - Consider the reaction of acetic acid in water...Ch. 7 - Prob. 32ECh. 7 - Prob. 33ECh. 7 - Prob. 34ECh. 7 - Prob. 35ECh. 7 - Values of Kw as a function of temperature are as...Ch. 7 - Prob. 37ECh. 7 - Prob. 38ECh. 7 - Prob. 39ECh. 7 - Prob. 40ECh. 7 - Prob. 41ECh. 7 - Prob. 42ECh. 7 - Prob. 43ECh. 7 - A solution is prepared by adding 50.0 mL of 0.050...Ch. 7 - Prob. 45ECh. 7 - Prob. 46ECh. 7 - Prob. 47ECh. 7 - Prob. 48ECh. 7 - Calculate the concentration of all species present...Ch. 7 - Prob. 50ECh. 7 - Prob. 51ECh. 7 - Prob. 52ECh. 7 - Prob. 53ECh. 7 - Prob. 54ECh. 7 - A solution is prepared by dissolving 0.56 g of...Ch. 7 - At 25°C a saturated solution of benzoic acid (see...Ch. 7 - Prob. 57ECh. 7 - Prob. 58ECh. 7 - A solution contains a mixture of acids: 0.50 M HA...Ch. 7 - Prob. 60ECh. 7 - Prob. 61ECh. 7 - Prob. 62ECh. 7 - Prob. 63ECh. 7 - Prob. 64ECh. 7 - Prob. 65ECh. 7 - Trichloroacetic acid (CCl3CO2H) is a corrosive...Ch. 7 - Prob. 67ECh. 7 - Prob. 68ECh. 7 - Prob. 69ECh. 7 - Prob. 70ECh. 7 - Prob. 71ECh. 7 - Prob. 72ECh. 7 - Prob. 73ECh. 7 - Prob. 74ECh. 7 - Prob. 75ECh. 7 - Prob. 76ECh. 7 - Prob. 77ECh. 7 - Prob. 78ECh. 7 - Prob. 79ECh. 7 - Prob. 80ECh. 7 - Calculate the pH of a 0.20 M C2H5NH2 solution...Ch. 7 - Prob. 82ECh. 7 - Prob. 83ECh. 7 - Prob. 84ECh. 7 - Prob. 85ECh. 7 - Quinine (C20H24N2O2) is the most important...Ch. 7 - Prob. 87ECh. 7 - Prob. 88ECh. 7 - Prob. 89ECh. 7 - Prob. 90ECh. 7 - Prob. 91ECh. 7 - Prob. 92ECh. 7 - Prob. 93ECh. 7 - Prob. 94ECh. 7 - A typical vitamin C tablet (containing pure...Ch. 7 - Prob. 96ECh. 7 - Prob. 97ECh. 7 - Prob. 98ECh. 7 - Prob. 99ECh. 7 - Prob. 100ECh. 7 - Rank the following 0.10 M solutions in order of...Ch. 7 - Prob. 102ECh. 7 - Prob. 103ECh. 7 - Prob. 104ECh. 7 - Prob. 105ECh. 7 - Prob. 106ECh. 7 - Prob. 107ECh. 7 - Prob. 108ECh. 7 - Prob. 109ECh. 7 - Prob. 110ECh. 7 - Prob. 111ECh. 7 - Prob. 112ECh. 7 - Prob. 113ECh. 7 - Prob. 114ECh. 7 - Prob. 115ECh. 7 - Prob. 116ECh. 7 - Prob. 117ECh. 7 - Prob. 118ECh. 7 - Prob. 119ECh. 7 - Prob. 120ECh. 7 - Prob. 121ECh. 7 - Prob. 122ECh. 7 - Calculate the pH of a 7.0107M HCl solution.Ch. 7 - Calculate the pH of a 1.0107M solution of NaOHin...Ch. 7 - Prob. 125AECh. 7 - Prob. 126AECh. 7 - Prob. 127AECh. 7 - Prob. 128AECh. 7 - Hemoglobin (abbreviated Hb) is a protein that is...Ch. 7 - Prob. 130AECh. 7 - Prob. 131AECh. 7 - Prob. 132AECh. 7 - Prob. 133AECh. 7 - Prob. 134AECh. 7 - Prob. 135AECh. 7 - Prob. 136AECh. 7 - Prob. 137AECh. 7 - One mole of a weak acid HA was dissolved in 2.0 L...Ch. 7 - Prob. 139AECh. 7 - Prob. 140AECh. 7 - Prob. 141AECh. 7 - Will 0.10 M solutions of the following salts be...Ch. 7 - Prob. 143AECh. 7 - Prob. 144AECh. 7 - Prob. 145AECh. 7 - Prob. 146AECh. 7 - Prob. 147AECh. 7 - Prob. 148AECh. 7 - Prob. 149AECh. 7 - Prob. 150AECh. 7 - Prob. 151AECh. 7 - Prob. 152CPCh. 7 - Prob. 153CPCh. 7 - A typical solution of baking soda (sodium...Ch. 7 - Prob. 155CPCh. 7 - Prob. 156CPCh. 7 - Prob. 157CPCh. 7 - Prob. 158CPCh. 7 - Prob. 159CPCh. 7 - Prob. 160CPCh. 7 - Prob. 161CPCh. 7 - Prob. 162CPCh. 7 - Prob. 163CPCh. 7 - Prob. 164CPCh. 7 - Prob. 165CPCh. 7 - Prob. 166CPCh. 7 - Prob. 167CPCh. 7 - Prob. 168CPCh. 7 - Prob. 169MP
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- What is the reaction mechanism for this?arrow_forwardWhat is the reaction mechanism for this?arrow_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. + Drawing Arrows CH3ONA, CH3OH heat : Br:O Na → H H Br Na + H H H H H :0: .H + Undo Reset Done Q CH3 Drag To Pan +arrow_forward
- What is the reaction mechanism for this?arrow_forward20.19 Predict the structure of the major 1,2-addition product formed by reaction of one mole of Cl₂ with 3-methylenecyclohexene. Also predict the structure of the 1,4-addition product formed under these conditions. 20.20 Which of the two molecules shown do you expect to be the major product formed by 1,2-addition of HCI to cyclopentadiene? Explain. Cyclopentadiene + HC 3-Chlorocyclopentene (racemic) or 4-Chlorocyclopentene (racemic)arrow_forward20.35 Propose structural formulas for compounds A and B and specify the configuration of compound B. EtO₂C 250°C C14H2004 CO₂Et 1. Oso, then NaHSO3 2. HIO4 C14H2006 A Barrow_forward
- 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.arrow_forwardAdd 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. + I I H CH3 Ph Досн Br OCH 3 Drawing Q H Atoms, Bonds and Rings Charges Tap a node to see suggestions. H H H H H Undo Reset Remove Done Rotatearrow_forward20.17 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.arrow_forward
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