Does 2-Methyl-2-Pentene Have Stereoisomers?

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The discussion centers on the stereoisomerism of 2-methyl-2-pentene, specifically whether it has E and Z forms. Participants express confusion regarding the question's wording and the definition of isomers, particularly distinguishing between structural and geometric isomers. Initial answers eliminate options based on the assumption of multiple structural isomers existing, leading to debates about the correct classification. The consensus leans toward the idea that the question pertains specifically to 2-methyl-2-pentene rather than all C6H12 compounds. Ultimately, clarity on the definition of isomers is essential for determining the correct answer.
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Homework Statement



The compound 2-methyl-2-pentene:

Select one:
a. has no structural or geometric isomers
b. has 2 structural alkene isomers, each of which has an E isomer and a Z isomer form.
c. has 5 structural isomers
d. has 3 structural isomers
e. exists as E and Z isomers

The Attempt at a Solution



So the wording of this question confuses me a bit, I took that when it said the compound 2-methyl-2-pentene it was just talking about c6h12 - if this is not the case and I've understood it horribly wrong please inform me :)

So straight away I cross out A just because it's obvious that at least 1 structural isomer exists. I then eliminate C and D because there are more than 5 structural isomers. I then cross out B because there are more than 2 alkene isomers 1/2/3-hexene eg. So I guess I would go with E as my answer. I know it's an easy question but I always overthink them and end up getting them wrong so this is more to help me understand the question and clear up any misconceptions I may have. Thanks
 
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E is definitely not a correct answer, draw the molecule - does it have E, Z isomers?
 
Borek said:
E is definitely not a correct answer, draw the molecule - does it have E, Z isomers?

Damn you're 100% right! I had that originally but then I started to think of the question as talking about all C6H12 molecules. I'm a but confused as what constitutes an isomer in relation to this question - I assume it's not talking about all C6H12 isomers so does that mean it's only taking about the location of the double bond and methyl group? Is it C then? It seems to have a large number of structural isomers to me.
 
TBH, I am not sure what the correct answer is - I don't have time to investigate, and just intuition is not enough. To me it looks like it talks about all C6H12 molecules.
 
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