BURDGE CHEMISTRY VALUE ED (LL)
4th Edition
ISBN: 9781259995958
Author: VALUE EDITION
Publisher: MCG CUSTOM
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Question
Chapter 24, Problem 61QP
Interpretation Introduction
Interpretation:
The contact process used for obtaining sulfuric acid is to be described.
Concept introduction:
Sulphuric acid is the most important industrial chemical.
It is colorless, syrupy liquid, also known as oil of vitriol.
It has a high boiling point and high viscosity.
It is a diprotic acid.
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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 24 Solutions
BURDGE CHEMISTRY VALUE ED (LL)
Ch. 24 - Prob. 1QPCh. 24 - Prob. 2QPCh. 24 - Prob. 3QPCh. 24 - Prob. 4QPCh. 24 - Prob. 5QPCh. 24 - Describe two laboratory and two industrial...Ch. 24 - Prob. 7QPCh. 24 - Prob. 8QPCh. 24 - Prob. 9QPCh. 24 - Prob. 10QP
Ch. 24 - Elements number 17 and 20 form compounds with...Ch. 24 - Give an example of hydrogen as (a) an oxidizing...Ch. 24 - Prob. 13QPCh. 24 - Prob. 14QPCh. 24 - Prob. 15QPCh. 24 - Prob. 16QPCh. 24 - Prob. 17QPCh. 24 - Prob. 18QPCh. 24 - Prob. 19QPCh. 24 - Prob. 20QPCh. 24 - Briefly discuss the preparation and properties of...Ch. 24 - Prob. 22QPCh. 24 - Prob. 23QPCh. 24 - Prob. 24QPCh. 24 - Prob. 25QPCh. 24 - Prob. 26QPCh. 24 - Prob. 27QPCh. 24 - Prob. 28QPCh. 24 - Prob. 29QPCh. 24 - Prob. 30QPCh. 24 - 24.31 Sodium hydroxide is hygroscopic-that is. it...Ch. 24 - Prob. 32QPCh. 24 - Prob. 33QPCh. 24 - 24.34 Describe a laboratory and an industrial...Ch. 24 - Prob. 35QPCh. 24 - Prob. 36QPCh. 24 - Prob. 37QPCh. 24 - Prob. 38QPCh. 24 - Prob. 39QPCh. 24 - Prob. 40QPCh. 24 - Prob. 41QPCh. 24 - Prob. 42QPCh. 24 - Prob. 43QPCh. 24 - Prob. 44QPCh. 24 - Prob. 45QPCh. 24 - Prob. 46QPCh. 24 - Prob. 47QPCh. 24 - Prob. 48QPCh. 24 - Prob. 49QPCh. 24 - Prob. 50QPCh. 24 - Prob. 51QPCh. 24 - Prob. 52QPCh. 24 - Prob. 53QPCh. 24 - Prob. 54QPCh. 24 - Prob. 55QPCh. 24 - Prob. 56QPCh. 24 - Describe one industrial and one laboratory...Ch. 24 - Prob. 58QPCh. 24 - Prob. 59QPCh. 24 - Prob. 60QPCh. 24 - Prob. 61QPCh. 24 - Prob. 62QPCh. 24 - Prob. 63QPCh. 24 - Prob. 64QPCh. 24 - Prob. 65QPCh. 24 - Prob. 66QPCh. 24 - Prob. 67QPCh. 24 - Prob. 68QPCh. 24 - Prob. 69QPCh. 24 - Prob. 70QPCh. 24 - Prob. 71QPCh. 24 - Prob. 72QPCh. 24 - Prob. 73QPCh. 24 - Prob. 74QPCh. 24 - Prob. 75QPCh. 24 - 24.76 Describe two reactions in which sulfuric...Ch. 24 - Prob. 77QPCh. 24 - Prob. 78QPCh. 24 - Prob. 79QPCh. 24 - Prob. 80QPCh. 24 - Prob. 81QPCh. 24 - Prob. 82QPCh. 24 - Prob. 83QPCh. 24 - Prob. 84QPCh. 24 - Prob. 85QPCh. 24 - Prob. 86QPCh. 24 - Prob. 87QPCh. 24 - Prob. 88QPCh. 24 - Prob. 89APCh. 24 - Prob. 90APCh. 24 - Prob. 91APCh. 24 - Prob. 92APCh. 24 - Prob. 93APCh. 24 - Prob. 94APCh. 24 - Prob. 95APCh. 24 - 24.96 Consider the Frasch process, (a) How is it...Ch. 24 - Prob. 97APCh. 24 - Prob. 98APCh. 24 - Prob. 99APCh. 24 - Life evolves to adapt to its environment. In this...Ch. 24 - Prob. 101APCh. 24 - Prob. 102APCh. 24 - Prob. 103APCh. 24 - Prob. 104APCh. 24 - Prob. 1SEPPCh. 24 - Prob. 2SEPPCh. 24 - Prob. 3SEPPCh. 24 - Prob. 4SEPP
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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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