Organic Chemistry Tutor Ben Wilson Shares With Us His Secret - Make Diastereomers From Organic Acids

Organic Chemistry Tutor Ben Wilson Shares With Us His Secret - Make Diastereomers From Organic AcidsOrganic chemistry tutor Ben Wilson shares with us how to make a very profitable dia ­teromer. You could have never dreamed that you could develop something like this.Ben Wilson is an organic chemistry tutor who has developed a liquid carbon dioxide dia ­teromer which he believes can be the next great material for liquid CO2 conversion. He believes that the liquid carbon dioxide is the starting point of carbon dioxide conversion, and he believes that dia ­teromers made from CO2 are likely to be more efficient than CO2 monomers. And he is correct.The idea of diastereomers was first conceived by Ben Wilson when he was a graduate student in organic chemistry, and he wrote this article with organic chemistry tutor, Timothy Wood for his article on diastereomers. The ideas were given to him by others, but the details are his own.Diastereomer is the chemical name for a monomer that is bonded t o both a carboxylate group and an alcohol group, or an ester group and a hydroxyl group. Normally, if you apply heat to these two compounds, then the monomer bonds to each one at a different place, resulting in a diastereomeric compound. This is a simple example, but it does illustrate the concept. By using diastereomers, each molecule can form two bonds, instead of just one.Ben Wilson believes that carbon dioxide is the starting point of liquid CO2 conversion, and he believes that diastereomers made from CO2 are likely to be more efficient than CO2 monomers. And he is correct.In organic chemistry, ben Wilson has made diastereomers from carbon dioxide and alcohols in the same method ashe has made other simple diastereomers. There are some things to consider here. His diastereomeric materials for liquid CO2 conversion are not as efficient as he would like them to be.Ben Wilson has used a pressure-chemical process for developing his diastereomers. But there are other ways to make dias tereomers, which will produce better results. The key is to make a diastereomer from a simple monomer, while still keeping the two atoms close together. Ben Wilson believes that this can be done easily.As the solvent molecules in the reaction are mostly O molecules, they will be tightly bound together. And because the molecules are highly electronegative, they will interact more strongly with the solvent, making a close bond between the alcohol and carboxylate. The idea of diastereomers has been well known for over twenty years, but the question of whether to make diastereomers from organic acids has been unanswered for sometime.