00:01
Hi, in this question we are having two parts.
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In the first part of the question we are given with these four isomeric hydrocarbons and we are asked to arrange them in increasing order of their stability.
00:11
The first compound we are having is cis -1 ,4 -dimethylcyclohexane.
00:17
This is the chair form of the cis -1 ,4 -dimethylcyclohexane.
00:22
The second compound is 1 -cyclopropylpentane.
00:27
This is the structure.
00:28
The third compound is ethylcyclohexane and the fourth compound is cis -1 -ethyl -2 -propylcyclopropane.
00:37
Here we can say that the stability of the six -membered ring is greater than three -membered ring because in three -membered ring there is strain.
00:54
Now in six -membered ring when it present in chair form then we can say that there is presence of 1 ,3 -diaxial interaction.
01:04
That is this is the first carbon and this is third carbon.
01:08
Here we are having ch3 and this hydrogen of ch3 interacts with this hydrogen that is present at the third position and this will create the steric hindrance.
01:21
Here also we have hydrogen and here we have ch3.
01:25
Then due to 1 ,3 -diaxial interaction we can see there is steric hindrance hence we can say that the stability is decreases in this case.
01:44
Now if we see the third compound which is also in the chair form here we have ethylcyclohexane.
01:51
This ethyl group is present on the equatorial position hence we can say that there is no 1 ,3 -diaxial interaction.
02:02
Therefore we can say that the stability of this compound is greater than the first one.
02:09
Now we have to decide between second and third.
02:13
Here we are having a three -membered ring which is attached on the pentane chain and in the fourth compound we are having a three -membered ring on which two groups are present as a substituent in the cis position...