Please explain the different reaction b/w these two...
I think these two reaction are E2. Why do they have different product?
Does the reaction follow the Zaltsev's rule?
The reason the top one takes the hydrogen off of the top carbon is because it's such a big base (it's going to go for the least sterically hindered carbon)
The bottom one is a small base so it can eliminate according to Zaitsev's rule
The reason the top one takes the hydrogen off of the top carbon is because it's such a big base (it's going to go for the least sterically hindered carbon)
The bottom one is a small base so it can eliminate according to Zaitsev's rule
Yes, so top 1 (the base) is branched which means it won't be able to get in that close to the secondary carbon.
Remember when the H comes off, the Br won't be there (first step is Br leaves) so the methyl (primary) will be an easy reach. I doubt you need to know that this occurs, but you should understand why it occurs.
GOOD LUCK