So, three questions:
1. I know double bond adjacency to a carbocation is stabilizing. Are carbanions also stabilized by an adjacent double bond?
2. Why is the E2 favored product of CH3(CH2)15CH2CH2Br +(CH3)3CO-K+ lead to CH3(CH2)15CH=CH2?
Finally, when adding a bromo tert butate to ethanol, what is the point of including Et-O-Na+ ?
I'm a new poster, so please let me know if there's some place these questions have already been answered or if I forgot something important in the post.