
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Transcribed Image Text:19. Complete the following reactions.
a. CH3CH=CHCH3 + H2
C.
+ Cl₂
FeC 13.
Pt
CH₂=CHCHCH=CH + 2C12
нансност
CH 3
b.
d.
CH3
CH3C=CH₂
CH3
+ 02
spark
Expert Solution

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Step 1
(a) Addition of hydrogen lead to formation of alkane.
(b) addition of Cl2 will occur on double bond.
(c) Addition of Cl2 on benzene will lead to the formation of electrophilic addition.
(d) Addition of O2 on alkene will lead to the formation of epoxide ring.
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- O Reagents Available a. CH₂=CHCH₂CI, AICI 3 CH3 b. CH₂Br₂, OH™ C. CH3CH₂COCI, AICI 3 d. H₂, Pt e. NBS, CCI4 f. K* tBuO™ g. CO, HCI, CUCI/AICI3 h. CH3CH₂CH₂COCI, AICI 3 i. BrCH₂CH₂Br, OH- j. CH3CH₂CI, AICI 3 k. RCO3H I. H3O+ Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol). Select reagents from the table in the order that you wish to use them, i.e. aced; do not include punctuation or spaces. If more than one route exists, choose the shorter one; in no case will a synthesis require more than 5 steps.arrow_forwardLl.60.arrow_forwardH Br. H₂CH₂C H H Br t-BuOK t-BuOH "Br CH3 H NaCN DMF CH₂CH3 (CH3)3COarrow_forward
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