00:01
In this question, we have two compounds.
00:04
So that is three bromose, one butin.
00:08
So if you see, this is a butin.
00:11
So one butin, there is a bromine is present.
00:18
So this is three bromine, one butin.
00:25
And the second compound is the same.
00:29
One bromide 1 -2 butin they are given so here it is 1 -promote 2 -butin so on it is undergoing sn1 reaction nucleophilic substitution reaction isn't 1 reaction even though both are unshable carbocatins they are forming if it undergoes sn1 reaction, it produces secondary carbocation.
01:15
And if you see for this one, it will produce the carbocatian here.
01:24
Here it will produce, which is a primary carbocatian, which is not stable, carbocatian, which is unstable.
01:36
So what happens here? here, the rearrangement will take place.
01:41
So the bond is taking place this side...