Foundations of College Chemistry 15e Binder Ready Version + WileyPLUS Registration Card
15th Edition
ISBN: 9781119231318
Author: Morris Hein
Publisher: Wiley (WileyPLUS Products)
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Chapter 11, Problem 6PE
Interpretation Introduction
Interpretation:
The size of an atom changes when it forms anion, reason for this changes has to be explained.
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Consider this step in a radical reaction:
Y
What type of step is this? Check all that apply.
Draw the products of the step on the right-hand side of the drawing area
below. If more than one set of products is possible, draw any set.
Also, draw the mechanism arrows on the left-hand side of the drawing
area to show how this happens.
ionization
propagation
initialization
passivation
none of the above
22.16 The following groups are ortho-para directors.
(a)
-C=CH₂
H
(d)
-Br
(b)
-NH2
(c)
-OCHS
Draw a contributing structure for the resonance-stabilized cation formed during elec-
trophilic aromatic substitution that shows the role of each group in stabilizing the
intermediate by further delocalizing its positive charge.
22.17 Predict the major product or products from treatment of each compound with
Cl₁/FeCl₂-
OH
(b)
NO2
CHO
22.18 How do you account for the fact that phenyl acetate is less reactive toward electro-
philic aromatic substitution than anisole?
Phenyl acetate
Anisole
CH
(d)
Chapter 11 Solutions
Foundations of College Chemistry 15e Binder Ready Version + WileyPLUS Registration Card
Ch. 11.1 - Prob. 11.1PCh. 11.2 - Prob. 11.2PCh. 11.3 - Prob. 11.3PCh. 11.4 - Prob. 11.4PCh. 11.4 - Prob. 11.5PCh. 11.5 - Prob. 11.6PCh. 11.6 - Prob. 11.7PCh. 11.6 - Prob. 11.8PCh. 11.7 - Prob. 11.9PCh. 11.8 - Prob. 11.10P
Ch. 11.9 - Prob. 11.11PCh. 11.10 - Prob. 11.12PCh. 11 - Prob. 1RQCh. 11 - Prob. 2RQCh. 11 - Prob. 3RQCh. 11 - Prob. 4RQCh. 11 - Prob. 5RQCh. 11 - Prob. 6RQCh. 11 - Prob. 7RQCh. 11 - Prob. 8RQCh. 11 - Prob. 9RQCh. 11 - Prob. 10RQCh. 11 - Prob. 11RQCh. 11 - Prob. 12RQCh. 11 - Prob. 13RQCh. 11 - Prob. 14RQCh. 11 - Prob. 15RQCh. 11 - Prob. 16RQCh. 11 - Prob. 17RQCh. 11 - Prob. 18RQCh. 11 - Prob. 19RQCh. 11 - Prob. 20RQCh. 11 - Prob. 21RQCh. 11 - Prob. 22RQCh. 11 - Prob. 23RQCh. 11 - Prob. 24RQCh. 11 - Prob. 25RQCh. 11 - Prob. 26RQCh. 11 - Prob. 28RQCh. 11 - Prob. 30RQCh. 11 - Prob. 31RQCh. 11 - Prob. 33RQCh. 11 - Prob. 36RQCh. 11 - Prob. 1PECh. 11 - Prob. 2PECh. 11 - Prob. 3PECh. 11 - Prob. 4PECh. 11 - Prob. 5PECh. 11 - Prob. 6PECh. 11 - Prob. 7PECh. 11 - Prob. 8PECh. 11 - Prob. 9PECh. 11 - Prob. 10PECh. 11 - Prob. 11PECh. 11 - Prob. 12PECh. 11 - Prob. 13PECh. 11 - Prob. 14PECh. 11 - Prob. 15PECh. 11 - Prob. 16PECh. 11 - Prob. 17PECh. 11 - Prob. 18PECh. 11 - Prob. 19PECh. 11 - Prob. 20PECh. 11 - Prob. 21PECh. 11 - Prob. 22PECh. 11 - Prob. 23PECh. 11 - Prob. 24PECh. 11 - Prob. 25PECh. 11 - Prob. 26PECh. 11 - Prob. 27PECh. 11 - Prob. 28PECh. 11 - Prob. 29PECh. 11 - Prob. 30PECh. 11 - Prob. 31PECh. 11 - Prob. 32PECh. 11 - Prob. 33PECh. 11 - Prob. 34PECh. 11 - Prob. 35PECh. 11 - Prob. 36PECh. 11 - Prob. 37PECh. 11 - Prob. 38PECh. 11 - Prob. 39PECh. 11 - Prob. 40PECh. 11 - Prob. 47PECh. 11 - Prob. 48PECh. 11 - Prob. 49PECh. 11 - Prob. 50PECh. 11 - Prob. 51PECh. 11 - Prob. 52PECh. 11 - Prob. 55AECh. 11 - Prob. 56AECh. 11 - Prob. 57AECh. 11 - Prob. 58AECh. 11 - Prob. 59AECh. 11 - Prob. 63AECh. 11 - Prob. 64AECh. 11 - Prob. 65AECh. 11 - Prob. 66AECh. 11 - Prob. 67AECh. 11 - Prob. 68AECh. 11 - Prob. 76AECh. 11 - Prob. 77AECh. 11 - Prob. 78AECh. 11 - Prob. 81AECh. 11 - Prob. 82AECh. 11 - Prob. 83AECh. 11 - Prob. 84AECh. 11 - Prob. 85AECh. 11 - Prob. 86AECh. 11 - Prob. 87AECh. 11 - Prob. 88CECh. 11 - Prob. 89CECh. 11 - Prob. 90CECh. 11 - Prob. 92CECh. 11 - Prob. 93CECh. 11 - Prob. 94CECh. 11 - Prob. 95CE
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- Show how to convert ethyl benzene to (a) 2,5-dichlorobenzoic acid and (b) 2,4-dichlorobenzoic acid.arrow_forwardHelp me solve this problem. Thank you in advance.arrow_forward22.7 Predict the monoalkylated products of the following reactions with benzene. (a) AlCl3 Ya (b) AlCl3 (c) H3PO4 (d) 22.8 Think-Pair-Share AICI3 The reaction below is a common electrophilic aromatic substitution. SO3 H₂SO4 SO₂H (a) Draw the reaction mechanism for this reaction using HSO,+ as the electrophile. (b) Sketch the reaction coordinate diagram, where the product is lower in energy than the starting reactant. (c) Which step in the reaction mechanism is highest in energy? Explain. (d) Which of the following reaction conditions could be used in an electrophilic aro- matic substitution with benzene to provide substituted phenyl derivatives? (i) AICI3 HNO3 H₂SO4 K2Cr2O7 (iii) H₂SO4 (iv) H₂PO₁arrow_forward
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- V Consider this step in a radical reaction: Br: ? What type of step is this? Check all that apply. Draw the products of the step on the right-hand side of the drawing area below. If more than one set of products is possible, draw any set. Also, draw the mechanism arrows on the left-hand side of the drawing area to show how this happens. ⚫ionization termination initialization neutralization none of the abc Explanation Check 80 Ο F3 F1 F2 2 F4 01 % do5 $ 94 #3 X 5 C MacBook Air 25 F5 F6 66 ©2025 ˇ F7 29 & 7 8arrow_forwardShow how to convert ethyl benzene to (a) 2,5-dichlorobenzoic acid and (b) 2,4-dichlorobenzoic acid.arrow_forwardno aiarrow_forward
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