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When pure (S)-lactic acid is esterified by racemic

Chapter 14, Problem 38SP

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QUESTION:

When pure (S)-lactic acid is esterified by racemic butan-2-ol, the product is 2-butyl lactate, with the following structure:

(a) Draw three-dimensional structures of the two stereoisomers formed, specifying the configuration at each asymmetric carbon atom. (Using your models may be helpful.)

(b) Determine the relationship between the two stereoisomers you have drawn.

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QUESTION:

When pure (S)-lactic acid is esterified by racemic butan-2-ol, the product is 2-butyl lactate, with the following structure:

(a) Draw three-dimensional structures of the two stereoisomers formed, specifying the configuration at each asymmetric carbon atom. (Using your models may be helpful.)

(b) Determine the relationship between the two stereoisomers you have drawn.

ANSWER:

Solution:

Step 1

(a)Here we have to draw three-dimensional structures of the two stereoisomers of lactic acid and  butan-2-ol formed  the product is 2-butyl lactate

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