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0 votes
0 answers
68 views

Which substrates will undergo an E2 reaction to give a (Z) alkene?

What I do know: E2 reactions are concerted and have an anti-coplanar transition state, where the leaving group and the hydrogen being abstracted have a dihedral angle of 180 degrees. What I don't ...
Dylan's user avatar
  • 7
3 votes
0 answers
277 views

Chugaev and Selenoxide Elimination giving different products

In class we are going over intramolecular elimination. In this question I will provide two similar reactants that provide a different mixture of products. The chugaev elimination gives a 50/50 ...
Brian M.'s user avatar
6 votes
1 answer
16k views

Why does d/l-2,3-dibromobutane on reaction with NaI/acetone give cis-2-butene?

This is what I have read/know about the dehalogenation of vicinal dihalides by NaI/acetone: The two halides which are leaving must be on opposite sides (from the mechanism). In case they are present ...
user600016's user avatar
  • 1,027
4 votes
1 answer
835 views

Elimination mechanism in alkenes

Do E2 elimination reactions occur in alkenes? If not, what mechanism is used? If they do, are they limited by any stereochemical rules as alkanes do (antiperiplanar)? My question is pernitent to the ...
Diracc's user avatar
  • 343