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Draw the major organic substitution product(s) for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile....

Draw the major organic substitution product(s) for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile. Indicate the stereochemistry, including H's, at each stereogenic center. Omit any byproducts.

Draw the major organic substitution product(s) for


Draw the major organic substitution product(s) for(2R, 3S)-2-bromo-3-methylepentane reacting with the given nucleophile. Indicate the stereochemistry, including H's, at each stereogenic center. Omit any byproducts.

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\((2 R, 3 S)-2\) -Bromo- 3 -methylpentane has two chiral centers. Ethoxide ion reacts with substrate by \(\mathrm{S}_{\mathrm{N}} 2\) mecahnism to form \((2 S, 3 S)-2\) -ethoxy- 3 -methylpentane. In the product, the configuration of chiral center at \(2^{\text {nd }}\) carbon is changed.

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