No, they should always have chiral centers
Recall that First, we must identify the CHIRAL center(s). This is done via --> chiral center rule:
it must be bonded to 4 different types of "branches" that is, they should NOT repeat each other, such as CH3, CH3.. It should have all 4 substituents completely different.
if they repeat, they are not CHIRAL centers, therefore, they become achiral... in which they CANT be stereoisomerism on meso/entantiomers
Note that there is a point in which the molecule can be non-chiral, but the centers must be chiral
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