Talk:Ether: Difference between revisions
Jump to navigation
Jump to search
→2-methoxybutane (Bretta McCall): new section |
|||
| (5 intermediate revisions by 5 users not shown) | |||
| Line 9: | Line 9: | ||
[[File:Ether.png]] | [[File:Ether.png]] | ||
== Alkene to Ether: Formation of 2-methoxy-2-methylbutane (Yuwei Pan) == | |||
[[File:2-methoxy-2-methylbutane.png|1000px]] | |||
== 1-methoxy-1-methylcyclohexane by oxymercuration (Kelsey Zhang) == | |||
[[File: Alcohol_by_Hg_ring.png|1100px]] | |||
The formation of 1-methoxy-1-methylcyclohexane first by oxymercuration, then the alcohol attack and break the three-membered ring on the more saturated C, and finally the borohydride substitute the mercury. | |||
== Synthesis of Chromenone from Chalcone(Nannan Ji) == | |||
[[File:Chromenone_synthesis.png]] | |||
== Diels-Alder (Xinming Li) == | |||
[[File:Diels-Alder.png|800px]] | |||
== Ether formation by epoxide (Siyuan Du) == | |||
[[File:Ester_from_epoxide.png|1100px]] | |||
Latest revision as of 02:30, 12 May 2018
Trityl ether (Grace Park)
2-methoxybutane (Bretta McCall)
Alkene to Ether: Formation of 2-methoxy-2-methylbutane (Yuwei Pan)
1-methoxy-1-methylcyclohexane by oxymercuration (Kelsey Zhang)
The formation of 1-methoxy-1-methylcyclohexane first by oxymercuration, then the alcohol attack and break the three-membered ring on the more saturated C, and finally the borohydride substitute the mercury.
Synthesis of Chromenone from Chalcone(Nannan Ji)
Diels-Alder (Xinming Li)
Ether formation by epoxide (Siyuan Du)
