Answer:it will be malfunction
Explanation:
Answer:
The final product of the reaction is (<em>2S,3S</em>)-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.
Answer:
A.
Explanation:
The paper clip allows elictricity to pass, unlike the eraser or paper
Roughness of the surface and weight of the object.
A) sodium fluoride
B) rubidium oxide
C) boron trichloride
D) dihydrogen selenide
E) tetraphosphate hexoxide
F) iodine trichloride