LAB EXPERIMENTS FOR CHEM >C<
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ISBN: 9781323912027
Author: Brown
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Chapter 20, Problem 53E
Interpretation Introduction
To determine: The value of
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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 20 Solutions
LAB EXPERIMENTS FOR CHEM >C<
Ch. 20.1 - What is the reducing agent in the following...Ch. 20.1 - Prob. 20.1.2PECh. 20.2 - Prob. 20.2.1PECh. 20.2 - Prob. 20.2.2PECh. 20.2 - Prob. 20.3.1PECh. 20.2 - Prob. 20.3.2PECh. 20.3 - Prob. 20.4.1PECh. 20.3 - Prob. 20.4.2PECh. 20.4 - Prob. 20.5.1PECh. 20.4 - The standard cell potential is 1.46 V for a...
Ch. 20.4 - Prob. 20.6.1PECh. 20.4 - Prob. 20.6.2PECh. 20.4 - Prob. 20.7.1PECh. 20.4 - Prob. 20.7.2PECh. 20.4 - Prob. 20.8.1PECh. 20.4 - Practice Exercise 2
Using Table 20.1, rank...Ch. 20.5 - Practice Exercise 1
Which of the following...Ch. 20.5 - Prob. 20.9.2PECh. 20.5 - Prob. 20.10.1PECh. 20.5 - Prob. 20.10.2PECh. 20.6 - Prob. 20.11.1PECh. 20.6 - Prob. 20.11.2PECh. 20.6 - Prob. 20.12.1PECh. 20.6 - Prob. 20.12.2PECh. 20.6 - Prob. 20.13.1PECh. 20.6 - Prob. 20.13.2PECh. 20.9 - Prob. 20.14.1PECh. 20.9 - Prob. 20.14.2PECh. 20 - Prob. 1DECh. 20 - Prob. 1ECh. 20 - 20.2 You may have heard that “antioxidants” are...Ch. 20 - Prob. 3ECh. 20 - Prob. 4ECh. 20 - Prob. 5ECh. 20 - Prob. 6ECh. 20 - 20.7 Consider a redox reaction for which Eo is a...Ch. 20 - Prob. 8ECh. 20 - Prob. 9ECh. 20 - Prob. 10ECh. 20 - Prob. 11ECh. 20 - Prob. 12ECh. 20 - 20.13
What is meant by the term oxidation?
On...Ch. 20 - Prob. 14ECh. 20 - Prob. 15ECh. 20 - Prob. 16ECh. 20 - Prob. 17ECh. 20 - Prob. 18ECh. 20 - Prob. 19ECh. 20 - Prob. 20ECh. 20 - Prob. 21ECh. 20 - Prob. 22ECh. 20 - Complete and balance the following half-reactions....Ch. 20 - Complete and balance the following half-reaction,...Ch. 20 - Complete and balance the following equations, and...Ch. 20 - Complete and balance the following equations, and...Ch. 20 - Prob. 27ECh. 20 - Prob. 28ECh. 20 - Prob. 29ECh. 20 - Prob. 30ECh. 20 - Prob. 31ECh. 20 - Prob. 32ECh. 20 - Prob. 33ECh. 20 - Prob. 34ECh. 20 - Prob. 35ECh. 20 - Prob. 36ECh. 20 - Prob. 37ECh. 20 - Prob. 38ECh. 20 - Prob. 39ECh. 20 - Prob. 40ECh. 20 - Prob. 41ECh. 20 - Prob. 42ECh. 20 - Prob. 43ECh. 20 - Prob. 44ECh. 20 - Prob. 45ECh. 20 - Prob. 46ECh. 20 - Assuming standard conditions, arrange the...Ch. 20 - Prob. 48ECh. 20 - Prob. 49ECh. 20 - Prob. 50ECh. 20 - Prob. 51ECh. 20 - For each of the following reactions, write a...Ch. 20 - Prob. 53ECh. 20 - Prob. 54ECh. 20 - Prob. 55ECh. 20 - Prob. 56ECh. 20 - A cell has a standard cell potential of +0.177 V...Ch. 20 - Prob. 58ECh. 20 - Prob. 59ECh. 20 - Prob. 60ECh. 20 - Prob. 61ECh. 20 - Prob. 62ECh. 20 - Prob. 63ECh. 20 - A voltaic cell utilizes the following reaction:...Ch. 20 - Prob. 65ECh. 20 - Prob. 66ECh. 20 - Prob. 67ECh. 20 - Prob. 68ECh. 20 - Prob. 69ECh. 20 - Prob. 70ECh. 20 - Prob. 71ECh. 20 - 20. 72 A voltaic cell is constructed that is based...Ch. 20 - Prob. 73ECh. 20 - Prob. 74ECh. 20 - Prob. 75ECh. 20 - Prob. 76ECh. 20 - Prob. 77ECh. 20 - In some applications nickel-cadmium batteries have...Ch. 20 - Prob. 79ECh. 20 - Prob. 80ECh. 20 - Prob. 81ECh. 20 - Prob. 82ECh. 20 - Prob. 83ECh. 20 - Prob. 84ECh. 20 - Prob. 85ECh. 20 - Prob. 86ECh. 20 - Prob. 87ECh. 20 - Prob. 88ECh. 20 - Prob. 89ECh. 20 - Prob. 90ECh. 20 - Prob. 91ECh. 20 - Metallic magnesium can be made by the electrolysis...Ch. 20 - 20.93
Calculate the mass of Li formed by...Ch. 20 - Prob. 94ECh. 20 - Prob. 95ECh. 20 - Prob. 96ECh. 20 - Prob. 97AECh. 20 - Prob. 98AECh. 20 - Prob. 99AECh. 20 - [20.100] Gold exists in two common positive...Ch. 20 - Prob. 101AECh. 20 - Prob. 102AECh. 20 - Prob. 103AECh. 20 - Prob. 104AECh. 20 - Prob. 105AECh. 20 - Prob. 106AECh. 20 - Prob. 107AECh. 20 - Prob. 108AECh. 20 - Prob. 109AECh. 20 - Prob. 110AECh. 20 - Prob. 111IECh. 20 - Prob. 112IECh. 20 - Prob. 113IECh. 20 - Prob. 114IECh. 20 - Prob. 115IECh. 20 - Prob. 116IECh. 20 - Prob. 117IECh. 20 - Prob. 118IECh. 20 - Prob. 119IE
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- + C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forward→ Acetyl-CoA + 3NAD+ + 1FAD + 1ADP 2CO2 + CoA + 3NADH + 1FADH2 + 1ATP a. Which of the above are the reactants? b. Which of the above are the products? c. Which reactant is the electron donor? d. Which reactants are the electron acceptors? e. Which of the products are now reduced? f. Which product is now oxidized? g. Which process was used to produce the ATP? h. Where was the energy initially in this chemical reaction and where is it now that it is finished? i. Where was the carbon initially in this chemical reaction and where is it now that it is finished? j. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. OCH 3 (Choose one) OH (Choose one) Br (Choose one) Explanation Check NO2 (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Aarrow_forward
- 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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