(R)-2-bromooctane undergoes alkaline hydrolysis to yield (S)-2-octanol – InterviewSolution

1.	(R)-2-bromooctane undergoes alkaline hydrolysis to yield (S)-2-octanol. Predict the stereochemistry (inversion or retention) of the reaction.
Answer» Solution :`##CHY_CHE_ORG_XII_P2_U10_E01_073_S01.png" width="80%"> Inversion of CONFIGURATION occurs.

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