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.

the equation that correctly represent the reaction for formation of ammonia is

n2+ 3h2 → 2nh3 (answer d)

1 mole of nitrogen gas (n2) react with 3 moles of hydrogen gas (h2) to form 2 moles of ammonia ( nh3). this is in a process known as haber process were iron is used as a catalyst and reaction take place that a higher temperature and pressure. the process is exothermic hence energy is released.

answer is: naturally occurring solid, inorganic compound or element is mineral.

minerals usually have crystalline form, that means than crystal constituents (atoms, molecules or ions) are arranged in a highly ordered microscopic structure, forming a crystal lattice that extends in all directions.

for example magnetite is a mineral of iron oxide (fe₂o₃).

calcite is a carbonate mineral and the most stable polymorph of calcium carbonate (caco₃).

dolomite is an   carbonate mineral composed of calcium magnesium carbonate (camg(co₃)₂).