



To identify which of the given pairs of compounds are enantiomers, we need to understand what enantiomers are in the context of organic chemistry. Enantiomers are a type of stereoisomer: molecules that are mirror images of each other but cannot be superimposed onto each other, much like left and right hands. These typically occur when a molecule has a chiral center — a carbon atom bonded to four different groups.
Let's analyze the provided options to determine which pair forms enantiomers:
The above displayed pair of compounds are mirror images of each other. To confirm they are enantiomers, check if they have a chiral center that makes them non-superimposable mirror images. This requires ensuring that the orientation around the chiral center in each compound is different in terms of stereochemistry (R/S configuration).
Through this analysis, it's been confirmed that the first pair forms enantiomers as they meet the criterion of being non-superimposable mirror images, while the other pairs either do not form mirror images, or are superimposable.
Therefore, the correct answer is:
In conclusion, understanding the concept of chirality and mirror image relationships helps identify enantiomers, which are pivotal in stereochemistry and many biological interactions.
What is the IUPAC name of the given haloarene? 