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.

The final product of the reaction is (2S,3S)-2-ethoxy-3-methylpentane.

Explanation:

The given reaction undergoes  mechanism in which the nucleophile attacks the backside and it is substituted by the elimination of bromine.

Due to the backside attack of nucleophile , the inverse in stereo-chemistry is observed.

After the substitution of ethoxy group, the configuration is assigned according to the priority it shows clock wise direction(R) - configuration.

When hydrogen faces the front side , it results shows inverse configuration i.e, S- configuration.

The chemical reaction is as follows.

why is cellular respiration important for homeostasis?

it changes food into energy that the organism can use.

which of the following is most likely to happen if a cell is not able to divide?

the cell will not be replaced when it is damaged.

explanation:

all eukaryotic cell have mitochondria : )