Most Stable Isomer: Ortho, Meta, or Para Benzene?

[skull]

Which of the following is most stable. Ortho, meta, or para benzene? Also, why is this the case.
Thank you in advance

 

[DDS]

your question makes no sense seing as benzen has no substituants to compare stability. And no hydrogens don't count as substituants

 

[DDS]

you may want to check the question just incase you may have miss-spelt the compound.

For example ortho-di-chlorobenzene can be compared to meta or para dichlorobenze in terms of stabilites

 

[skull]

OMG sorry about that! I forgot to include the branch names. Assume the branches are bromine

 

[DDS]

well then that makes things a lot more clearer...know assuming you know how the orth meta and para positions look like on a molecule and the trend for increasing ionic radius you can further deduce that bromine is a fairly large molecule thus it wants its space otherwise if forced to close to another large molecule it would make it unstable.

From this i think you can figure out which orientation is the most stable