Your hands are mirror images
Hold your hands palm to palm: they match. Now lay one on top of the other, both palms down: the thumbs point opposite ways. No turn makes them fit. Many molecules are like that. Below is one, alanine (a building block of proteins), and its mirror image. Drag to turn them.
- one hand (solid)
- mirror hand (hatched)
Structures: PubChem (NCBI), compounds , public domain. Letters on the balls: C carbon, N nitrogen, O oxygen; small balls are hydrogen.
A catalyst that is 75% one hand and 25% the mirror hand: how big is the product's lead of one hand?
A catalyst speeds up a reaction without being used up. A handed catalyst makes more of one hand of the product. Chemists measure the lead of one hand as the excess (ee, enantiomeric excess): 75 to 25 is an excess of 50% (75 minus 25). A catalyst that is all one hand gives a product with some best excess; call that 100% here.
Pick one first.
Start with a head start of five parts in ten million. After three runs, how much of one hand?
In 1995 Kenso Soai's group showed a reaction whose product is the catalyst for making more of itself, copies its own hand, and pulls further ahead each time (his first self-copying reaction, in 1990, lost its lead instead). In 2003 they started it with an almost even mix: an excess of one hand of only 0.00005%, prepared on purpose. That is five parts in ten million. Each run's product was the start of the next run.
Pick one first.
Start perfectly balanced. Run it 1,000 times. What do you get?
Now take a toy reaction that starts with no handed molecules at all. Plain molecules slowly turn into one hand or the mirror hand at the same rate. Each handed molecule copies its own hand. And when a molecule meets its mirror image, the two lock into an idle mixed pair (chemists call this mutual antagonism). Nothing favours either hand.
Pick one first.
Medicines, and a very old question
Many medicines come in two mirror forms. The Nobel Committee's popular explanation says one form can have the
effect you want, while the mirror form can cause unnecessary and sometimes harmful side effects
. So chemists
need reactions that make one hand on purpose, and Kagan's non-linear effects help them understand and tune those
reactions.
Life itself is one-handed: your proteins use one hand of each amino acid. How that began is still open.
Soai's reaction shows that a flask can pick a hand by chance and keep it, but the Committee is clear that this kind of
model is not an answer to the origin of biological homochirality
.