Asked by Madeline Armes on Sep 25, 2024

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How many distinct alkene products results when 1-bromo-1-ethylcyclopentane is treated with NaOCH3?

A) 1
B) 2
C) 3
D) 4

Alkene Products

Compounds resulting from reactions involving alkenes, typically characterized by the presence of double bonds in their structure.

Cyclopentane

A cyclic hydrocarbon with the formula C5H10, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms.

  • Project the consequences of alkene synthesis reactions, detailing the array of conceivable outcomes and their stereochemistry.
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victoria garcia4 days ago
Final Answer :
B
Explanation :
Treatment of 1-bromo-1-ethylcyclopentane with NaOCH3 would result in elimination of HBr to form one or more alkene products. Since there are two β-carbons available for elimination, two different alkene products can be formed: 1-ethylcyclopentene and 3-ethylcyclopentene. However, these two alkene products are constitutional isomers and not stereoisomers, so they are considered distinct from one another. Therefore, the answer is B) 2.