Above reaction is an example of 
AEsterification
BSaponification
CHydrolysis
DTrans Esterification
Answer & Solution
Correct answer: D. Trans Esterification
The reaction shows an ester reacting with an alcohol in the presence of $\mathrm{HCl}$, and the alkoxy group of the ester changes from $\mathrm{OMe}$ to the propyl group while $\mathrm{MeOH}$ is formed as a by-product. This is exchange of the ester alkoxy group by another alcohol, which is called $\text{transesterification}$. Therefore the correct option is $\mathrm{D}$.
Related questions
Order of boiling points of the given compound is:
(1) pentan-1-ol
(2) butan-1-ol
(3) butaIn the following aromatic compound, bromination in presence of $Fe$ occurs preferentially Given the diazonium salt shown, which product is formed on treatment with $NaNO_2$, Cu andNitrobenzene gives hydroxylamine by-
![](https://qallery.app/diagrams/v2_46c8b1655a73/imgThe correct IUPAC name of the compound,
![](https://qallery.app/diagrams/v2_248e9aa17a93/Which of the following resonating structures of 1-methoxy-1, 3-butadiene is least stable$$\mathrm{CH_3-CH=CH-CH=CH-C_2H_5}$$ isBenzene on treatment with a mixture of conc. $$\mathrm{HNO_3}$$ and conc. $$\mathrm{H_2SO_