00:01
Hello students, in this question we have to tell the correct isomeric relationships between the given molecules.
00:07
Let's look at the first example.
00:10
In the first example we have two cyclohexane chair forms which contain the first chair form contains two methyl group at one two carbons.
00:21
However the second chair form contains methyl groups at one and three carbons.
00:29
So we can see that the atoms to which these different methyl groups are bonding are different.
00:36
So they will be referred as constitutional isomers.
00:45
Now let's look at second example.
00:49
Our second example contains this molecule given in the newman's form.
00:55
So let's first convert it into a wedge dash projection.
00:59
Consider that this molecule is rotated through an axis going through this front carbon like this.
01:07
Hence we will get a molecule which will contain hydroxyl group here.
01:12
Ch3 will go below the plane and this hydrogen will come above the plane and here we will have a ch2 group or we can simply draw it like this.
01:26
Now let's rotate this sigma bond to bring this methyl group on the left side.
01:35
Therefore this molecule will become oh group here.
01:39
This ch2et group will be on the left side and this methyl group will come above the plane and hydrogen will go behind the plane.
01:54
Similarly is the second molecule also contain a hydrogen atom behind the plane.
01:59
Now these are our two molecules.
02:02
We can see that they are mirror images of each other.
02:07
However they are not superimposable.
02:10
They will be our enantiomers.
02:17
Now let's look at the third example.
02:21
In the third example, we have given this cyclohexane and chair form of another molecule of cyclohexane.
02:28
So let's first convert this wedge dash projection into a chair form as well...