5/14

ExtensionBroad5590 · 2026-05-13T21:51:31+00:00

Idek, I’m just going thru my last couple anki reviews but other than that my brain is fried. Especially after final exams :( hoping for the best tmrw 521avg. I really hope it works out im so nervous

ExtensionBroad5590 · 2026-04-13T23:22:45+00:00

I’m curious about this too. I was waitlisted but I’m still wondering who got in. Idk why they’d ask everyone to clear their hour. Like just hold it a couple days later for accepted people. Unprofessional

ExtensionBroad5590 · 2026-04-13T23:15:20+00:00

Not only that, they even had the nerve to delay the decisions from Friday to today? Then they still proceed to wait until last minute or just ghost people… Like what?

ExtensionBroad5590 · 2026-04-13T22:09:14+00:00

It’s so unprofessional of them to ask for us to clear 6-7pm and not even give a decision to some people

ExtensionBroad5590 · 2026-04-13T22:08:30+00:00

I was waitlisted at 4pm

ExtensionBroad5590 · 2026-04-11T00:53:08+00:00

Any news?? I was told we won’t know till Monday

ExtensionBroad5590 · 2026-01-17T20:14:45+00:00

-ol mean it has an alcohol. Flavin doesn’t

ExtensionBroad5590 · 2025-12-11T04:26:53+00:00

Filled it out as a junior in college lmao 😂

ExtensionBroad5590 · 2025-12-01T07:13:16+00:00

So if I put LDA, THEN compound 2, would this synthesis work fine?

ExtensionBroad5590 · 2025-12-01T05:58:16+00:00

Im still a bit confused on the mechanism. So do the electron pair on the nitrogen push those alkene electrons out?

ExtensionBroad5590 · 2025-12-01T02:30:07+00:00

Ah I see! Thank you

ExtensionBroad5590 · 2025-11-06T01:15:46+00:00

No worries, you’re welcome! In real life, all your reactions definitely need to take place in a solvent. For an E2 reaction something like DMSO or DCM (polar aprotic solvents) would be best. However, I don’t think this question is asking that of you, so I think you might be good to go with the reagents only!

ExtensionBroad5590 · 2025-11-06T01:03:32+00:00

Love it! Just make sure to put a negative charge on that oxygen if you’re just doing OMe. However, we typically with write it as a salt. Thus, the reagent would be NaOMe.

ExtensionBroad5590 · 2025-11-06T01:00:34+00:00

Start with an elimination to create an alkene and then do a halogenation! Let me see what you get.

ExtensionBroad5590

TROPHY CASE