In these processes where LTA is briefly violated the molecules will soon
find themselves elsewhere where LTE is again valid. In general, you
can't build something on the molecular scale at some point without
molecules farther away interfering with what is going on (unless you
have sophisticated machinery already present to exploit the process,
like in case of photosynthesis). So, a process that initially breaks
chiral symmetry in one way will soon undergo interactions with other
nearby molecules that will cause the process to go in the other
direction. On the long term such effects will then get averaged out.
The fundamental problem you then have is that with only simple molecules
you are subject to the Eigen limit. All you can do is to get to polymers
that can contain information that can copy themselves using template
copying. But the error rate per copied part then defines the maximum
amount of information that can be contained, for realistic systems this
is way too small to code for a sophisticated error correction system.
Without such systems the error rate will thus remain high and you can
never get to the biological world.
If instead you already have forged very large molecules in
micro-environments (that are themselves also made out of organics), you
can circumvent the Eigen limit due to the size of the molecules.
Information can also be present in the larger scale properties of
molecules that can be copied far more accurately. This possibility is
not directly available in conventional prebiotic models, because of the
small size of the molecules one starts out with. They have to resort to
very complex models involving such things as autocatalytic sets to evade
this problem but that brings in a whole host of other problems.
Saibal