
Physical Chemistry
2nd Edition
ISBN: 9781285969770
Author: Ball
Publisher: Cengage
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Chapter 10, Problem 10.58E
Interpretation Introduction
Interpretation:
The validation of the given statement is to be stated.
Concept introduction:
In
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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 10 Solutions
Physical Chemistry
Ch. 10 - State the postulates of quantum mechanics...Ch. 10 - Prob. 10.2ECh. 10 - State whether the following functions are...Ch. 10 - State whether the following functions are...Ch. 10 - Prob. 10.5ECh. 10 - Prob. 10.6ECh. 10 - Evaluate the operations in parts a, b, and f in...Ch. 10 - The following operators and functions are defined:...Ch. 10 - Prob. 10.9ECh. 10 - Indicate which of these expressions yield...
Ch. 10 - Indicate which of these expressions yield an...Ch. 10 - Why is multiplying a function by a constant...Ch. 10 - Prob. 10.13ECh. 10 - Using the original definition of the momentum...Ch. 10 - Under what conditions would the operator described...Ch. 10 - A particle on a ring has a wavefunction =12eim...Ch. 10 - Calculate the uncertainty in position, x, of a...Ch. 10 - For an atom of mercury, an electron in the 1s...Ch. 10 - Classically, a hydrogen atom behaves as if it were...Ch. 10 - The largest known atom, francium, has an atomic...Ch. 10 - How is the Bohr theory of the hydrogen atom...Ch. 10 - Though not strictly equivalent, there is a similar...Ch. 10 - The uncertainty principle is related to the order...Ch. 10 - Prob. 10.24ECh. 10 - Prob. 10.25ECh. 10 - For a particle in a state having the wavefunction...Ch. 10 - Prob. 10.27ECh. 10 - A particle on a ring has a wavefunction =eim,...Ch. 10 - Prob. 10.29ECh. 10 - Prob. 10.30ECh. 10 - Prob. 10.31ECh. 10 - Normalize the following wavefunctions over the...Ch. 10 - Prob. 10.33ECh. 10 - Prob. 10.34ECh. 10 - For an unbound or free particle having mass m in...Ch. 10 - Prob. 10.36ECh. 10 - Prob. 10.37ECh. 10 - Prob. 10.38ECh. 10 - Evaluate the expression for the total energies for...Ch. 10 - Prob. 10.40ECh. 10 - Verify that the following wavefunctions are indeed...Ch. 10 - In exercise 10.41a, the wavefunction is not...Ch. 10 - Prob. 10.43ECh. 10 - Prob. 10.44ECh. 10 - Explain why n=0 is not allowed for a...Ch. 10 - Prob. 10.46ECh. 10 - Prob. 10.47ECh. 10 - Prob. 10.48ECh. 10 - Carotenes are molecules with alternating CC and...Ch. 10 - The electronic spectrum of the molecule butadiene,...Ch. 10 - Prob. 10.51ECh. 10 - Prob. 10.52ECh. 10 - Show that the normalization constants for the...Ch. 10 - Prob. 10.54ECh. 10 - Prob. 10.55ECh. 10 - An official baseball has a mass of 145g. a...Ch. 10 - Is the uncertainty principle consistent with our...Ch. 10 - Prob. 10.58ECh. 10 - Prob. 10.59ECh. 10 - Instead of x=0 to a, assume that the limits on the...Ch. 10 - In a plot of ||2, the maximum maxima in the plot...Ch. 10 - Prob. 10.62ECh. 10 - Prob. 10.63ECh. 10 - The average value of radius in a circular system,...Ch. 10 - Prob. 10.65ECh. 10 - Prob. 10.66ECh. 10 - Prob. 10.67ECh. 10 - Prob. 10.68ECh. 10 - Prob. 10.69ECh. 10 - Assume that for a particle on a ring the operator...Ch. 10 - Mathematically, the uncertainty A in some...Ch. 10 - Prob. 10.72ECh. 10 - Prob. 10.73ECh. 10 - Verify that the wavefunctions in equation 10.20...Ch. 10 - An electron is confined to a box of dimensions...Ch. 10 - a What is the ratio of energy levels having the...Ch. 10 - Consider a one-dimensional particle-in-a-box and a...Ch. 10 - Prob. 10.78ECh. 10 - Prob. 10.79ECh. 10 - Prob. 10.80ECh. 10 - Prob. 10.81ECh. 10 - What are x,y, and z for 111 of a 3-D...Ch. 10 - Prob. 10.83ECh. 10 - Prob. 10.84ECh. 10 - Prob. 10.85ECh. 10 - Prob. 10.86ECh. 10 - Prob. 10.87ECh. 10 - Prob. 10.88ECh. 10 - Substitute (x,t)=eiEt/(x) into the time-dependent...Ch. 10 - Write (x,t)=eiEt/(x) in terms of sine and cosine,...Ch. 10 - Prob. 10.91ECh. 10 - Prob. 10.92ECh. 10 - Prob. 10.93ECh. 10 - Prob. 10.95E
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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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