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(C) The reaction involves the electrophilic addition of $HBr$ to the alkene. The starting material contains a chiral center. Upon protonation of the d

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Diastereomers

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(C) The reaction involves the electrophilic addition of $HBr$ to the alkene. The starting material contains a chiral center. Upon protonation of the double bond,a carbocation is formed at the $C-2$ position. The subsequent attack of the bromide ion $(Br^-)$ can occur from either side of the planar carbocation,leading to the formation of two new chiral centers. Since the molecule already possesses one chiral center,the formation of a second chiral center results in the creation of two diastereomeric products. These products are not mirror images of each other and are therefore diastereomers.

What is the stereochemistry of the product formed in the following reaction?

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