00:01
Hello student, so the question is to draw the initial organic product of the bronsted acid base reaction.
00:08
So here let's first understand what is bronsted, bronsted acid.
00:16
So the bronsted acid is the one which donates, which donates h plus ions in the solution and the bronsted base is the one which accepts the h plus ions from the solution.
00:44
So here this cyclohexene is the bronsted base, so this is the base and here the h3o plus is the acid.
00:54
So here the h3o plus will donate h plus ions and the cyclohexene will accept the h plus ion which is donated by h3o plus.
01:07
Let's see the mechanism.
01:09
So here this is the base and now the base which will accept electron will be this pi bond, so here this pi bond will accept, attack this proton and this proton bond will shift towards the oxygen.
01:23
Now it will form, it will form this intermediate where the h plus is being, is being added, is being accepted by this cyclohexene base and here the carbocation ion is being formed.
01:40
Now again the water which is h2o which has the two lone pairs will attack this carbocationic center and will form, and will form this product...