Asked by Madeline Armes on Sep 25, 2024
Verified
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.
Verified Answer
VG
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.
Learning Objectives
- Project the consequences of alkene synthesis reactions, detailing the array of conceivable outcomes and their stereochemistry.
Related questions
Draw a Chair Conformation of the Starting Substituted Cyclohexane Molecule ...
A Reaction of an Unknown Alkene with MCPBA in Dichloromethane ...
Give the Structure of the Alkene Which Would Yield the ...
How Many Moles of Carbon Dioxide Are Generated When One ...
What Synthetic Goal Is Achieved by Subjecting an Alkene to ...