Problem 1. Triphenylmethane can be prepared by reaction of benzene and chloroform in the presence of AIC13. Propose a mechanism for the reaction. H. + CHCI3 AICI3 -C- 2016 Cengage Leaning Problem 2. The conversion of 3° alcohols into 3° alkyl halides under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows. (a) OH CI HCI (b) OH Br HBr (c) OH CI HCI e20 Cen ng
Problem 1. Triphenylmethane can be prepared by reaction of benzene and chloroform in the presence of AIC13. Propose a mechanism for the reaction. H. + CHCI3 AICI3 -C- 2016 Cengage Leaning Problem 2. The conversion of 3° alcohols into 3° alkyl halides under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows. (a) OH CI HCI (b) OH Br HBr (c) OH CI HCI e20 Cen ng
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![Problem 1.
Triphenylmethane can be prepared by reaction of benzene and chloroform in the presence of
AIC13. Propose a mechanism for the reaction.
H
AICI3
+
CHCI3
2016 Cengage Learning
Problem 2.
The conversion of 3° alcohols into 3° alkyl halides under acidic conditions involves two
cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.
(a)
OH
CI
HCI
(b)
ОН
Br
HBr
(c)
OH
CI
HCI
e201 Cengageleang](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa2161b10-ea5e-4583-9829-d7d2757b209e%2Fa3e344db-94df-491c-8f94-a27d374033ca%2F67cm8tn_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Problem 1.
Triphenylmethane can be prepared by reaction of benzene and chloroform in the presence of
AIC13. Propose a mechanism for the reaction.
H
AICI3
+
CHCI3
2016 Cengage Learning
Problem 2.
The conversion of 3° alcohols into 3° alkyl halides under acidic conditions involves two
cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.
(a)
OH
CI
HCI
(b)
ОН
Br
HBr
(c)
OH
CI
HCI
e201 Cengageleang
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