Answer:
The correct appropriate will be Option 1 (Acid anhydrides are less stable than esters so the equilibrium favors the ester product.)
Explanation:
- Acid anhydride, instead of just a carboxyl group, is typically favored for esterification. The predominant theory would be that Anhydride acid is somewhat more volatile than acid. This is favored equilibrium changes more toward the right of the whole ester structure.
- Extremely responsive than carboxylic acid become acid anhydride as well as acyl chloride. Thus, for esterification, individuals were most favored.
The other options offered are not relevant to something like the scenario presented. So, the solution here is just the right one.
Temperature
surface area
reactant concentration
Answer:
ethyl acetate layer
Explanation:
This question tests your knowledge of the principle of solvent extraction.
In solvent extraction, there is always an organic layer and an aqueous layer. The ethyl acetate is the organic layer while the sodium bicarbonate is the aqueous layer.
A brominated aromatic compound will be extracted into the organic layer (ethyl acetate layer).
Answer:
2
Explanation:
It is going through the air and is moving so that means that it has kinetic energy. But it is also going to go the down, which gives it potential energy.
