What is the basis for the successful resolution of racemic C₆H₅CHOHCO₂H through use of the chiral amine,C₆H₅CH(NH₂)CH₃? A)One enantiomer is more soluble than the other. B)The racemic mixture is converted into a single isomer in the basic solvent. C)The diastereomeric salts formed have different solubilities. D)The diastereomeric salts have different boiling points. E)The diastereomeric salts have different melting points.

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The chiral amine, C₆H₅CH(NH₂)CH₃, forms diastereomeric salts with the racemic mixture of C₆H₅CHOHCO₂H, resulting in two different products with different solubilities. This allows for separation of the enantiomers through a process called diastereomer crystallization. The diastereomer with higher solubility can be easily removed, leaving behind the pure enantiomer.

What Is the Basis for the Successful Resolution of Racemic