Explanation:
-Filter help — delete some big unreacted, undesirable species (norit is probably from what you are sorting through, its only carbon which cleans up things)
— extract with DCM because you are probably in an aqueous phase, and some butanoate is in it
- Anhydrous sodium absorbs excess of water (dries the material)
-evaporation in the hood to clear the DCM and crystallize the product.
Question
<em>Given the noble gas configuration of an element: [Ar] 4s2, 3d5, what is the element?
</em>
Answer:
<em>B.) Argon</em>
Hope this helps!
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: There are 20 protons neutrons in the atom
