1. Q3. Convert these names to structures: 1. 3-methyl-2-pentene 2. 4-cyclopropyl-2-hexene 3. (cis)-3-methyl-2-pentene 4. (trans)-1,2-dimethylcyclobutane 5. (E)-2-chloro-3-fluoro-2-pentene 6. (E)-2-chloro-3-fluoro-2-pentene Q4. Identify the most stable alkene in the following molecules: A B C D E Q5. Use arrow-pushing mechanism for the following rearrangements: 2. 6 d
1. Q3. Convert these names to structures: 1. 3-methyl-2-pentene 2. 4-cyclopropyl-2-hexene 3. (cis)-3-methyl-2-pentene 4. (trans)-1,2-dimethylcyclobutane 5. (E)-2-chloro-3-fluoro-2-pentene 6. (E)-2-chloro-3-fluoro-2-pentene Q4. Identify the most stable alkene in the following molecules: A B C D E Q5. Use arrow-pushing mechanism for the following rearrangements: 2. 6 d
World of Chemistry, 3rd edition
3rd Edition
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Chapter20: Organic Chemistry
Section: Chapter Questions
Problem 4STP
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Q3. Convert these names to structures:
1. 3-methyl-2-pentene
2. 4-cyclopropyl-2-hexene
3. (cis)-3-methyl-2-pentene
4. (trans)-1,2-dimethylcyclobutane
5. (E)-2-chloro-3-fluoro-2-pentene
6. (E)-2-chloro-3-fluoro-2-pentene
Q4. Identify the most stable alkene in the following molecules:
A
B
C
D
E
Q5. Use arrow-pushing mechanism for the following rearrangements:
2.
6
d"
Transcribed Image Text:1.
Q3. Convert these names to structures:
1. 3-methyl-2-pentene
2. 4-cyclopropyl-2-hexene
3. (cis)-3-methyl-2-pentene
4. (trans)-1,2-dimethylcyclobutane
5. (E)-2-chloro-3-fluoro-2-pentene
6. (E)-2-chloro-3-fluoro-2-pentene
Q4. Identify the most stable alkene in the following molecules:
A
B
C
D
E
Q5. Use arrow-pushing mechanism for the following rearrangements:
2.
6
d
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