Step 1: Understand acetylation.
During acetylation, each hydroxyl group $(-OH)$ is converted into acetate group $(-OCOCH_3)$.
Net increase in mass for one hydroxyl group is:
$$
CH_3CO - H = 43 - 1 = 42u
$$
So, each $-OH$ group increases molecular mass by $42u$.
Step 2: Total increase given.
Total increase in mass after complete acetylation:
$$
84u
$$
Step 3: Find number of hydroxyl groups.
$$
\text{Number of } -OH \text{ groups}=\frac{84}{42}=2
$$
Step 4: Identify carbohydrate with two hydroxyl groups.
Aldotriose structure:
$$
CHO-CHOH-CH_2OH
$$
It contains exactly two hydroxyl groups.
Step 5: Conclusion.
Hence the carbohydrate must be aldotriose.
$$
\therefore \text{Correct option is (A) Aldotriose.}
$$