J jd399 Full Member 10+ Year Member Joined Jun 14, 2009 Messages 156 Reaction score 0 Jul 5, 2009 #1 Members do not see this ad. why does the double bond go to the end and not the middle
Kneecoal Full Member 10+ Year Member Joined Mar 2, 2009 Messages 870 Reaction score 0 Jul 5, 2009 #2 i believe it's because you're using such a big base that you're going to get the less substituted alkene. can someone back me up on this? Upvote 0 Downvote
i believe it's because you're using such a big base that you're going to get the less substituted alkene. can someone back me up on this?
1 192LT192 Full Member 10+ Year Member Joined May 3, 2009 Messages 100 Reaction score 0 Jul 5, 2009 #3 Kneecoal said: i believe it's because you're using such a big base that you're going to get the less substituted alkene. can someone back me up on this? Click to expand... i dont know what the question is but you could get the less substituted alkene in the hofman elimination. you also get the less substituted one when doing E2 with a bulky base, namely (CH3)3CONa or LDA. so yeah youre right. Upvote 0 Downvote
Kneecoal said: i believe it's because you're using such a big base that you're going to get the less substituted alkene. can someone back me up on this? Click to expand... i dont know what the question is but you could get the less substituted alkene in the hofman elimination. you also get the less substituted one when doing E2 with a bulky base, namely (CH3)3CONa or LDA. so yeah youre right.