e.g.
If I draw a fischer projection of a compound with two chiral centers like this (vertically):
_CH3
I+OH
I+Cl
_COOH
("_" is meaningless, just for creating a space)
There is no problem to find the priorities of the substituents in the first (upper) chiral carbon.
However, the upper vertical branch of the second chiral carbon is out of screen (paper), and how about the carboxylic carbon? Out of screen?
We still follow the rules of fischer projection? So that, the structure bends into the screen just like forming a ring?