@chemmunity: How would you solve this synthesis problem? Let us know in the comments since there are many different ways! #chemistry #organicchemistry #premed #study #ochem
1. Hg(OAC)2, H2O 2.NaBH4 3. PCC 4. PH3PCH(CH3)2 5. NaH
2026-05-30 19:08:20
0
Шронк :
My synthesis is the same, but the last stage should be McMurry reaction of acetone
2026-03-15 16:02:10
2
crabrangoon :
hydration, PCC, TICl4/Reducing agent
2026-05-02 22:09:52
0
The chemistry icon :
it does whatever the hell it wants anyways, so no 💜
2026-03-16 17:59:14
2
HFhGBG :
I would probably go with HBr, make that a Grignard reagent, attack acetone and use heat on the hydrolysis step so the yielded alcohol transforms into the most substituted alkene via E1 🤔🤔
2026-03-15 15:54:26
3
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