WebAssign for Zumdahl's Chemical Principles, 8th Edition [Instant Access], Single-Term
8th Edition
ISBN: 9780357119112
Author: Zumdahl; Steven S.
Publisher: Cengage Learning US
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Chapter 7, Problem 70E
Interpretation Introduction
Interpretation: The order of given acids from strongest to weakest needs to be determined.
Concept Introduction: An acid is the substance that gives H+ or
The acid dissociation constant is the ratio of concentration of product and reactant for the equilibrium reaction of weak acid in solution. For the given weak acid HA, it can be written as:
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For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the
benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene.
Molecule
Inductive Effects
Resonance Effects
Overall Electron-Density
×
NO2
○ donating
O donating
O withdrawing
O withdrawing
O electron-rich
electron-deficient
no inductive effects
O no resonance effects
O similar to benzene
E
[
CI
O donating
withdrawing
O no inductive effects
Explanation
Check
○ donating
withdrawing
no resonance effects
electron-rich
electron-deficient
O similar to benzene
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Understanding how substituents activate
Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic
aromatic substitution.
Explanation
HN
NH2
Check
X
(Choose one)
(Choose one)
(Choose one)
(Choose one)
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Identifying electron-donating and electron-withdrawing effects on benzene
For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the
benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene.
Inductive Effects
Resonance Effects
Overall Electron-Density
Molecule
CF3
O donating
O donating
O withdrawing
O withdrawing
O no inductive effects
O no resonance effects
electron-rich
electron-deficient
O similar to benzene
CH3
O donating
O withdrawing
O no inductive effects
O donating
O withdrawing
Ono resonance effects
O electron-rich
O electron-deficient
O similar to benzene
Explanation
Check
Х
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Chapter 7 Solutions
WebAssign for Zumdahl's Chemical Principles, 8th Edition [Instant Access], Single-Term
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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- For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forwardIdentifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward
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