Each of the given molecules contains a chirality center. Determine the relationship between the molecules. three images of 1-phenyl-1-propanol are given as compound A, B and C. Compound A has a dashed bond to the alcohol group, with the phenyl group on the left side and the remaining carbon chain on the right. Compound B has a dashed bond to the alcohol group, with the phenyl group on the right side and the remaining carbon chain on the left. Compound C has a wedge bond to the alcohol group, with the phenyl group on the right side and the remaining carbon chain on the left. Compound D is 1-phenyl-2-propanol with a dashed bond to the alcohol group and the phenyl on the left side and the remaining single carbon on the right side. What is the relationship between A and B

They are enantiomers

Explanation:

So, according and based on the question, you want to know he relation only between A and B. I'll show you in the following drawing. If you want to know the relation with the others, post them on another question thread.

According to what you are stating here, we have a phenyl group on one side, then, the alcohol on one carbon, dashed (a side chain in the phenyl) and the rest of the chain on the same side. This will be compound A.

Compound B is the same as before, but the phenyl group on the other side. Like if you put Compound A in front of a mirror.

The key to know the relationship, is to see the chiral center. If the chiral center has the same configuration (R or S) as the other compound, then, both compounds could be the same molecule. If the configuration is different, then, we might facing enantiomers.

Let'´s see the original 1-phenyl-1-propanol, and formed compound A and B. (See picture below).

According to the picture, we can see that both compound has a different  configuration in the chiral center (R and then S), and the only different between them is the fact that the phenyl group is on the other side. This is just like a mirror, so we can conclude that A and B are enantiomers.

Hope this helps

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