Answer:
Esterification reaction
Explanation:
When we have to go from an acid to an ester we can use the <u>esterification reaction</u>. On this reaction, an alcohol reacts with a carboxylic acid on acid medium to produce an ester and water. (See figure).
In this case, we need the <u>methyl ester</u>, therefore we have to choose the <u>appropriate alcohol</u>, so we have to use the <u>methanol</u> as reactive if we have to produce the methyl ester.
"The reaction will absorb energy" is the best conclusion according to the energy diagram of the chemical reaction.
<u>Option: B</u>
<u>Explanation:</u>
The chemical bonds in the reactions are broken and formed as per process and contributed by three major steps: reactants, transition phase and product formation. Here transition phase is in equilibrium stage drived by activation energy, where bond is partially formed and partially broken, located at higher energy level then the starters.
The reactant's energy level is less relative to the products as seen in the endothermic reactions' energy diagram, which depicts that the products are less balanced than reactants. Here when the reaction is forced to the forward direction, then it direct towards the more unbalance entities. As energy is absorbed in the endothermic reaction from surrounding, thus the enthalpy change (ΔH) for the reaction is positive.
