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

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterNW2: Nomenclature Worksheet 2: Intro To Naming Functional Groups

Section: Chapter Questions

Problem 1CTQ: A student names the second structure above 2,3-dimethylcyclohex-1-ene. What rule does thisviolate?

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