LL ORG CHEM
6th Edition
ISBN: 9781264840083
Author: SMITH
Publisher: MCG
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Textbook Question
Chapter 13, Problem 54P
Consider the following bromination:
a. Calculate
b. Draw out a stepwise mechanism for the reaction, including the initiation, propagation, and termination steps.
c. Calculate
d. Draw an energy diagram for the propagation steps.
e. Draw the structure of the transition state of each propagation step.
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3. Why did breaking the P-C single bond lead to the formation of 2 species containing a
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4. Do you think the photoinitiator 2-hydroxy-2-methylpropiophenone would require a
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CH3
Figure 5: Structure of 2-hydroxy-2-
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that will be broken by light). (Taken from
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3417/3/2/490/htm)
ČH3
5. Why is the PEGDA monomer soluble in water, but the polymer is not? In other
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6. Thinking about the octet rule, why do you think many free radicals are very…
#9
Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction.
•
•
You do not have to consider stereochemistry.
•
Include all valence lone pairs in your answer.
Br2
Br
In cases where there is more than one answer, just draw one.
+
√n [
?
N
ZI
Chapter 13 Solutions
LL ORG CHEM
Ch. 13.1 - Prob. 1PCh. 13.1 - Prob. 2PCh. 13.2 - Prob. 3PCh. 13.3 - Prob. 4PCh. 13.3 - Prob. 5PCh. 13.4 - Prob. 7PCh. 13.5 - Problem 15.8 Which bond in the each compound is...Ch. 13.6 - Prob. 9PCh. 13.6 - Prob. 10PCh. 13.7 - Prob. 11P
Ch. 13.7 - Prob. 12PCh. 13.8 - Prob. 13PCh. 13.8 - Prob. 14PCh. 13 - Prob. 27PCh. 13 - Prob. 28PCh. 13 - Prob. 34PCh. 13 - 15.37 What alkane is needed to make each alkyl...Ch. 13 - 15.38 Which alkyl halides can be prepared in good...Ch. 13 - Prob. 37PCh. 13 - 15.40 Explain why radical bromination of p-xylene...Ch. 13 - a. What product(s) (excluding stereoisomers) are...Ch. 13 - Prob. 40PCh. 13 - 15.43 Draw the products formed when each alkene is...Ch. 13 - 15.44 Draw all constitutional isomers formed when...Ch. 13 - 15.45 Draw the organic products formed in each...Ch. 13 - Prob. 45PCh. 13 - 15.47 Treatment of a hydrocarbon A (molecular...Ch. 13 - 15.48 Draw the products formed in each reaction...Ch. 13 - 15.53 Consider the following bromination: .
a....Ch. 13 - 15.54 Draw a stepwise mechanism for the following...Ch. 13 - Prob. 57PCh. 13 - 15.57 Devise a synthesis of each compound from...Ch. 13 - Prob. 59PCh. 13 - Prob. 60PCh. 13 - 15.60 Devise a synthesis of each compound using ...Ch. 13 - Prob. 62PCh. 13 - Prob. 63PCh. 13 - 15.63 As described in Section 9.16, the...Ch. 13 - 15.64 Ethers are oxidized with to form...
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