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among the compound, choose the most stable alkene among the following, pent-2-ene, 2-methylbut-2-ene, pent-1-ene
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If we draw the structures we can better understand what's happening around each double-bond: |dw:1397655401122:dw|
The stability of an alkene is greater if there are more carbons attached to it--so a secondary alkene--one with two carbons attached--would be more stable than a primary alkene with just one carbon attached to it.
So whichever of the above three structures has the greatest number of carbons attached is the most stable. Since cis- and trans- orientations were not mentioned in the question, they don't have any effect on our answer.
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