Depends on the type of isomer. Structural (constitutional isomers) can often be resolved, as can cis/trans isomers. Eantiomeric compounds (mirror image isomers) are resolved on chiral media, but not general TLC plates. Some diastereomers can be resolved too on TLC.
If they are structural isomers so they are different in chemical environment so you have to select specific mobile and stationary phase. Enantiomers show different behavior only in chiral environment. If you select a stationary phase of TLC as chiral it may be possible, Normally silica gel is achiral it can converted into achiral stationary phase by a reaction with a chiral molecule. For column chromatography this very popular for TLC you have to search. After this i also think is their any possibility of chiral mobile phase if not possible to find chiral SP for TLC.
Depends on the type of isomer. Structural (constitutional isomers) can often be resolved, as can cis/trans isomers. Eantiomeric compounds (mirror image isomers) are resolved on chiral media, but not general TLC plates. Some diastereomers can be resolved too on TLC.
Historically, enantiomers can't be separated by TLC.
But, I think if you make a mixture between proportions of cellulose (or one of its derivatives), chitin, or other chiral polymers with silica, and preparing the TLC plates by using these mixtures.
You might succeed to separate some enentiomers.
I didn't try it by my self, but I think it might work!!!!
if these two molecules are diastereoisomers then it could be separated in two spots by using TLC over the use of appropriate mobile phase . if molecules are enanatiomers then it is impossible to sepaerate on TLC ,you can go for chiral HPLC.
from you question I assume that you can separate them as you know you have 2 products but just want to make sure if they are isomers? If you have a LCMS available and it separates them, then isomers would have the same mass. Otherwise you need to separate by any of the suggested methods and characterise further with MS, NMR,..