No, you're right Kate, I'm not interested. I've only spent the vast majority of my life embedded in a cult that has reinforced a dogmatic view of the world, discouraged knowledge and education and now that I have mentally freed myself from these shackles all I am interested in doing is remaining comfortable in my ignorance.
You are infuriating sometimes-K99
Lol I am sorry for making wrong assumptions. You are genuine. I see that xx.
If I understand what you have written correctly then in nature only the L/H molecule is produced by autocatalysis. How does the R/H molecule get formed then? What's the catalyst? - K99
Your question is very good, and clearly highlights how bad I am at explaining things at a layman's level, but it's good I can improve my skills.`
Enantiomers are stereo isomers that exist as molecules in chemicals and in nature. All matter is made up of chemical elements and molecules. All living things in nature have only the left handed molecule, all inanimate things have a racemic mixture. So the right handed molecule exists as part of the object just as much as the left handed molecule. But in the formation of amino acids only the left handed molecule is formed.
Normally to speed up or guide a reaction a chemical is used to do this that does not get used up in the chemical reaction, but in the case of autocatalysis the conditions produce the formation of only left handed molecules.There is no chemical that acts as a catalyst.
So what is your conclusion?