00:02
What alkenes are produced from the following alkohalides by an e1 reaction for a, our alkyohalide is a substituted chlorine, which if we draw it out, would be this molecule here, this be our alpha carbon, beta 1, beta 2, upon a elimination reaction, we will produce two substituted alkenes.
00:44
We will produce two substituted alkenes.
00:46
Will produce h3c, h2c, c, c, c, c, hh, ch, ch33.
01:06
So we get a tri -substituted alkene.
01:15
And we also produce a die -substituted alkyne plus hb.
01:59
So according to zydezav's rule, hp positive, the more substituted alkene is more stable and is the major product.
02:14
So according to zydezav's rule, the tri -substituted alken would be the major product, which would be this molecule here.
02:29
For our second molecule, we have click ring, substituted iodine.
02:44
And propyl group here...