Talk:Todd:Chem3x11 ToddL9

From OpenWetWare
Revision as of 06:47, 15 June 2013 by Matthew Todd (talk | contribs) (1st answer)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigationJump to search

Student question 2013: "When doing an epoxide opening on a trans-decalin derivative, can the trans-diequatorial product form at all, or is it impossible (since ring-flipping a trans-decalin is impossible)?" Answer: The decalin system is locked, as for when you have one ring and a tert-butyl. So yes, no ring flipping of the products. So you will get very significant selectivity for trans-diaxial, which stays trans-diaxial.