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Chemistry [hardcover]
5th Edition
ISBN: 9780393264845
Author: Geoffery Davies
Publisher: NORTON
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Question
Chapter 2, Problem 2.74QP
(a)
Interpretation Introduction
Interpretation: The chemical names of the given potassium compounds
Concept introduction: The nomenclature rule provides the systematic names to the chemical compounds. Ions which comprise of at least one or more than one atom are known as polyatomic ions.
To determine: The chemical name of
(b)
Interpretation Introduction
To determine: The chemical name of
(c)
Interpretation Introduction
To determine: The chemical name of
(d)
Interpretation Introduction
To determine: The chemical name of
(e)
Interpretation Introduction
To determine: The chemical name of
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Rank 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)
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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
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Identifying 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
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Chapter 2 Solutions
Chemistry [hardcover]
Ch. 2.3 - Prob. 1PECh. 2.3 - Prob. 2PECh. 2.4 - Prob. 3PECh. 2.5 - Prob. 4PECh. 2.6 - Prob. 5PECh. 2.6 - Prob. 6PECh. 2.7 - Prob. 7PECh. 2.7 - Prob. 8PECh. 2.7 - Prob. 9PECh. 2.7 - Prob. 10PE
Ch. 2.7 - Prob. 11PECh. 2 - Prob. 2.1VPCh. 2 - Prob. 2.2VPCh. 2 - Prob. 2.3VPCh. 2 - Prob. 2.4VPCh. 2 - Prob. 2.5VPCh. 2 - Prob. 2.6VPCh. 2 - Prob. 2.7VPCh. 2 - Prob. 2.8VPCh. 2 - Prob. 2.9VPCh. 2 - Prob. 2.10VPCh. 2 - Prob. 2.11QPCh. 2 - Prob. 2.12QPCh. 2 - Prob. 2.13QPCh. 2 - Prob. 2.14QPCh. 2 - Prob. 2.15QPCh. 2 - Prob. 2.16QPCh. 2 - Prob. 2.17QPCh. 2 - Prob. 2.18QPCh. 2 - Prob. 2.19QPCh. 2 - Prob. 2.20QPCh. 2 - Prob. 2.21QPCh. 2 - Prob. 2.22QPCh. 2 - Prob. 2.23QPCh. 2 - Prob. 2.24QPCh. 2 - Prob. 2.25QPCh. 2 - Prob. 2.26QPCh. 2 - Prob. 2.27QPCh. 2 - Prob. 2.28QPCh. 2 - Prob. 2.29QPCh. 2 - Prob. 2.30QPCh. 2 - Prob. 2.31QPCh. 2 - Prob. 2.32QPCh. 2 - Prob. 2.33QPCh. 2 - Prob. 2.34QPCh. 2 - Prob. 2.35QPCh. 2 - Prob. 2.36QPCh. 2 - Prob. 2.37QPCh. 2 - Prob. 2.38QPCh. 2 - Prob. 2.39QPCh. 2 - Prob. 2.40QPCh. 2 - Prob. 2.41QPCh. 2 - Prob. 2.42QPCh. 2 - Prob. 2.43QPCh. 2 - Prob. 2.44QPCh. 2 - Prob. 2.45QPCh. 2 - Prob. 2.46QPCh. 2 - Prob. 2.47QPCh. 2 - Prob. 2.48QPCh. 2 - Prob. 2.49QPCh. 2 - Prob. 2.50QPCh. 2 - Prob. 2.51QPCh. 2 - Prob. 2.52QPCh. 2 - Prob. 2.53QPCh. 2 - Prob. 2.54QPCh. 2 - Prob. 2.55QPCh. 2 - Prob. 2.56QPCh. 2 - Prob. 2.57QPCh. 2 - Prob. 2.58QPCh. 2 - Prob. 2.59QPCh. 2 - Prob. 2.60QPCh. 2 - Prob. 2.61QPCh. 2 - Prob. 2.62QPCh. 2 - Prob. 2.63QPCh. 2 - Prob. 2.64QPCh. 2 - Prob. 2.65QPCh. 2 - Prob. 2.66QPCh. 2 - Prob. 2.67QPCh. 2 - Prob. 2.68QPCh. 2 - Prob. 2.69QPCh. 2 - Prob. 2.70QPCh. 2 - Prob. 2.71QPCh. 2 - Prob. 2.72QPCh. 2 - Prob. 2.73QPCh. 2 - Prob. 2.74QPCh. 2 - Prob. 2.75QPCh. 2 - Prob. 2.76QPCh. 2 - Prob. 2.77QPCh. 2 - Prob. 2.78QPCh. 2 - Prob. 2.79QPCh. 2 - Prob. 2.80QPCh. 2 - Prob. 2.81QPCh. 2 - Prob. 2.82QPCh. 2 - Prob. 2.83QPCh. 2 - Prob. 2.84QPCh. 2 - Prob. 2.85QPCh. 2 - Prob. 2.86QPCh. 2 - Prob. 2.87QPCh. 2 - Prob. 2.88QPCh. 2 - Prob. 2.89QPCh. 2 - Prob. 2.90QPCh. 2 - Prob. 2.91QPCh. 2 - Prob. 2.92QPCh. 2 - Prob. 2.93QPCh. 2 - Prob. 2.94QPCh. 2 - Prob. 2.95QPCh. 2 - Prob. 2.96QPCh. 2 - Prob. 2.97QPCh. 2 - Prob. 2.98QPCh. 2 - Prob. 2.99QPCh. 2 - Prob. 2.100QPCh. 2 - Prob. 2.101QPCh. 2 - Prob. 2.102QPCh. 2 - Prob. 2.103QPCh. 2 - Prob. 2.104QPCh. 2 - Prob. 2.105QPCh. 2 - Prob. 2.106QPCh. 2 - Prob. 2.107APCh. 2 - Prob. 2.108APCh. 2 - Prob. 2.109APCh. 2 - Prob. 2.110APCh. 2 - Prob. 2.111APCh. 2 - Prob. 2.112APCh. 2 - Prob. 2.113APCh. 2 - Prob. 2.114APCh. 2 - Prob. 2.115APCh. 2 - Prob. 2.116APCh. 2 - Prob. 2.117APCh. 2 - Prob. 2.118APCh. 2 - Prob. 2.119APCh. 2 - Prob. 2.120APCh. 2 - Prob. 2.121APCh. 2 - Prob. 2.122APCh. 2 - Prob. 2.123APCh. 2 - Prob. 2.124APCh. 2 - Prob. 2.125APCh. 2 - Prob. 2.126APCh. 2 - Prob. 2.127APCh. 2 - Prob. 2.128AP
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- Rank 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_forwardAssign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Brarrow_forwarddescrive the energy levels of an atom and howan electron moces between themarrow_forward
- Tarrow_forwardPredict the major organic product(s) of the following reactions. Indicate which of the following mechanisms is in operation: SN1, SN2, E1, or E2.arrow_forward(c) (4pts) Mechanism: heat (E1) CH3OH + 1.5pts each _E1 _ (1pt) Br CH3OH (d) (4pts) Mechanism: SN1 (1pt) (e) (3pts) 1111 I H 10 Ill!! H LDA THF (solvent) Mechanism: E2 (1pt) NC (f) Bri!!!!! CH3 NaCN (3pts) acetone Mechanism: SN2 (1pt) (SN1) -OCH3 OCH3 1.5pts each 2pts for either product 1pt if incorrect stereochemistry H Br (g) “,、 (3pts) H CH3OH +21 Mechanism: SN2 (1pt) H CH3 2pts 1pt if incorrect stereochemistry H 2pts 1pt if incorrect stereochemistryarrow_forward
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