00:01
Hello students, here is the first question we have to find out the reagent and use it to convert the cyclo -hachnol into cyclo -hectomy.
00:09
Let us look.
00:10
When cyclo -hachnol is treated with tussar floreid, what will happen here? the tussal group will take up this position where such plus will leave.
00:26
Here it will be a plus state, here in mynest state.
00:28
And here we will get then intermediate states having like this.
00:34
That is, the social group will be here and there will be hydrogen.
00:39
And what happens here is that in the presence of periodine, this halidiv will be taken up by the periodine and here this hydrology will shift into here as a result of the torso group which is a bulky group will leave.
01:02
And as a result of that, here we will get our product having the structure like this, that is cyclohex3.
01:12
So here we can say that the reagent that used for the conversion of cycloachshkene into cyclohexene is option a, they are tussar, chloride and bdd.
01:29
This is the answer for the first question.
01:31
And the next question we have to write up, even alcohol in the increasing order of their reactivity to a dehydration.
01:38
The dehydration is taking place in the presence of halkyric acid.
01:41
In the case of the first molecule, the dehydration will be taken by strung here.
01:47
As a result, there will be formation of a double bond and the product will have the structure like this.
01:56
And the specialty of this product is that it is less substituted.
02:07
And when we consider our next alcohol, here also dehydration takes place...