
How many cyclopentane structures (excluding stereoisomers) are possible for${{C}_{7}}{{H}_{14}}$ .
Answer
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Hint:Cyclopentane is an organic chemical containing five carbon atoms present in a cyclic ring. Generally cyclic organic compounds up to five membered rings are less stable in nature when compared to aliphatic hydrocarbons of the same length.
Complete step-by-step answer:- In the question it is asked to draw the structures of cyclopentane that are possible with the molecular formula of ${{C}_{7}}{{H}_{14}}$ by excluding the stereoisomers.
- In the given molecular formula there are seven carbon atoms and fourteen hydrogen atoms are present.
- The basic structure of cyclopentane is as follows.
- Five carbon atoms are going to attached end to end each other.
- Stereoisomers are the isomers that have the same molecular formula and same sequence of bonds but they differ in three dimensional orientations.
- The possible cyclopentane structures with the molecular formula are as follows.
- There are only four possible cyclopentane structures by excluding the stereoisomers with the molecular formula of ${{C}_{7}}{{H}_{14}}$.
- Structure D and B can form two stereoisomers.
- Structure C and A can form one more stereoisomer with the same molecular formula ${{C}_{7}}{{H}_{14}}$.
- But we need the possible isomers by excluding stereoisomers.
- Therefore the possible cyclopentane structures are four only with molecular formula ${{C}_{7}}{{H}_{14}}$ by excluding stereoisomers.
Note: Stereoisomers are also called as spatial isomers; they have the same molecular formula but different three dimensional arrangements of atoms. Stereoisomers are mirror images and are optically active in nature.
Complete step-by-step answer:- In the question it is asked to draw the structures of cyclopentane that are possible with the molecular formula of ${{C}_{7}}{{H}_{14}}$ by excluding the stereoisomers.
- In the given molecular formula there are seven carbon atoms and fourteen hydrogen atoms are present.
- The basic structure of cyclopentane is as follows.
- Five carbon atoms are going to attached end to end each other.
- Stereoisomers are the isomers that have the same molecular formula and same sequence of bonds but they differ in three dimensional orientations.
- The possible cyclopentane structures with the molecular formula are as follows.
- There are only four possible cyclopentane structures by excluding the stereoisomers with the molecular formula of ${{C}_{7}}{{H}_{14}}$.
- Structure D and B can form two stereoisomers.
- Structure C and A can form one more stereoisomer with the same molecular formula ${{C}_{7}}{{H}_{14}}$.
- But we need the possible isomers by excluding stereoisomers.
- Therefore the possible cyclopentane structures are four only with molecular formula ${{C}_{7}}{{H}_{14}}$ by excluding stereoisomers.
Note: Stereoisomers are also called as spatial isomers; they have the same molecular formula but different three dimensional arrangements of atoms. Stereoisomers are mirror images and are optically active in nature.
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