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Question: What is the relationship between 1-butene and cis-2-butene. A) Enantiomers B) Diastereomers C)...

What is the relationship between 1-butene and cis-2-butene.
A) Enantiomers
B) Diastereomers
C) Identical
D) Constitutional isomers

Explanation

Solution

The given two molecules have the same molecular formula, but have different structures. The properties are also different. An enantiomer is a stereoisomer that's a non-superimposable mirror image of each other, and a diastereomer is a stereoisomer with two or more stereocenters, and the isomers are not mirrored images of each other.

Complete answer:
Enantiomers and Diastereomers are both types of stereoisomers. The structure of the given compound can be shown as:

From the structure it can be seen that the two molecules have the same molecular formula of C4H8{C_4}{H_8}. But differ in the position of the double bond. In 1butene1 - butene the double bond is between C1&C2{C_1}\& {C_2} and in cis2butenecis - 2 - butene the double bond is between C2&C3{C_2}\& {C_3}. The compounds that have the same molecular formula but differ in their connectivity are known as ‘Constitutional Isomers’.
Hence the correct answer is Option D.
Option A is incorrect because enantiomers are compounds that are mirror images of each other and are nonsuperimposable. Hence option A is wrong.
Option B is also incorrect because diastereomers are those compounds that are neither mirror images nor non-superimposable. But have almost the same structures that differ in their spatial arrangements.
Option C is incorrect because they are not identical.

Note:
Isomers are the compounds that have the same molecular formula but different arrangements of atoms in space (special arrangements). This difference can be brought about by the difference in bonding arrangements, constraint of rotation about a bond or difference in the direction in which the plane polarised light is rotated. The more the number of carbon atoms, in a molecule, the more isomers. Due to the change in arrangement their physical and chemical properties may change.