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.

(2R,3S)-2-ethoxy-3-methylpentane

and

(2S,3S)-2-ethoxy-3-methylpentane

Explanation:

For this case, we will have   as nucleophile. Also, this compound is also in excess. So, we will have as solvent a protic solvent. Therefore the Sn1 reaction would be favored.

The first step would be the carbocation formation followed by the attack of the nucleophile. In this case both isomers would be produced: R and S (see figure).

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answer:

the reaction is type of combination reaction.

explanation:

on the product side, there are 2 molecules of bonded to fe   which means one atom of fe are combined two molecules of . so, balanced chemical equation becomes :

this reaction follows the reaction type of combination reaction. a combination reaction is defined as chemical reaction in which reactants combines together to form a single product.