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Q.

The number of stereoisomers formed when (R)-2-methyl-3-chlorobutane is further monochlorinated is

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a

2

b

3

c

4

d

5

answer is C.

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Detailed Solution

The structure of (R)-2-methyl-3-chlorobutane is

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The monochlorination gives five products.

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The structure IV is achiral. The structure I is 2R, 3R. The structure II is 2S, 3R. The structure III is R. The structure Vis S.

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