Draw the structures of the $20$ common L$-$amino acids on a separate sheet of paper. Include the name, three$-$letter code, and single$-$letter code under each amino acid structure.

Create Fisher diagram representations for D$-$aldose triose, tetrose, pentose, and hexose sugars on another sheet of paper. Draw fifteen structures in total and provide the names.

On a different sheet of paper, sketch Haworth projections for D$-$Glucose and D$-$Galactose as pyranoses in their $\backslash$alpha $-$anomeric forms, and for D$-$Ribose and D$-$Fructose as furanoses in their $\backslash$beta $-$anomeric forms.

Illustrate the structures of lauric acid, myristic acid, palmitic acid, and stearic acid on a separate sheet.

Draw the structure of glycerol on its own sheet and highlight the differences from glyceraldehyde. Explain the type of chemical reaction $($oxidation or reduction$)$ that converts glyceraldehyde to glycerol.

On a separate sheet, draw the structures of oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, and pimelic acid. Additionally, devise a mnemonic device to aid in remembering the names of these dicarboxylic acid compounds in order.