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Anonymous Fri 18 Dec 19:15:55 2020 No.12480878 View Reply Original Report

Quoted By: >>12480901 >>12481002 >>12481044 >>12481092

Did I fucked up?

Anonymous

Anonymous Fri 18 Dec 2020 19:23:28 No.12480901 Report

Quoted By:

>>12480878
E2, base is small, 3 H-atoms at the terminal C and only one at the 2 position (sometimes the statistical stuff matters).
Not sure but I think it's probably the answer on the far right.

Anonymous

Anonymous Fri 18 Dec 2020 19:59:33 No.12481002 Report

Quoted By:

>>12480878
No if the primary carbon gets deprotonated the answer would be second from the right.
I think the zaitsev product would proceed though

Anonymous

Anonymous Fri 18 Dec 2020 20:08:29 No.12481044 Report

Quoted By: >>12481047

>>12480878
Pretty sure you're correct. Internal alkenes are more stable and the stereochemistry would prefer the Z product. Side note, fischer projections are fucking stupid and literally no one uses them besides sugar chemists

Anonymous

Anonymous Fri 18 Dec 2020 20:09:12 No.12481047 Report

Quoted By:

>>12481044
based and correct pilled

Anonymous

Anonymous Fri 18 Dec 2020 20:20:23 No.12481092 Report

Quoted By:

>>12480878
that's not a circle

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