A Stepwise Approach for the Synthesis of Folic Acid in the organic chemistry lab
A Stepwise Approach for the Synthesis of Folic Acid in the organic chemistry lab
combinatorial chemistry; ester synthesis Fundamentals of Organic Chemistry Lab Post-Lab Questions 1. If you were doing these experiments on a larger scale, describe two ways that you could improve the yield of the target ester What is the point of adding sulfuric acid to the reaction? How about the heat? 2. Pick your favorite of the esters you made, and write the mechanism for its formation. 3.
CREATINE SYNTHESIS ORGANIC CHEMISTRY LAB REPORT ***introduction questions**** 4: Give balanced equations for the synthesis of creatine from cyanamide and sarcosine
CREATINE SYNTHESIS ORGANIC CHEMISTRY LAB REPORT ***introduction questions**** 1: Give a brief introduction to what creatine is, its biological function, and the lab synthesis.
CREATINE SYNTHESIS ORGANIC CHEMISTRY LAB REPORT ***introduction questions**** 5: Give a detailed mechanism (show electron flow) for the synthesis of creatine from cyanamide and sarcosine.
Chem. 9: Organic Chemistry Lab Lab 10: Synthesis of Soap 4. Use the three components provided below to draw how soap works to remove greasy dirt. soopolar WWWWW grease molecule polar head nonpolar tail OW soap molecule 00- H water molecule
2. Folic acid is a molecule needed in the synthesis of nucleotides. Many bacteria have an enzyme that can bind the molecule, PABA, and catalyze its conversion into folic acid. Bacteria that cannot make folic acid will die. Sulfanilamide is an antibiotic used to treat certain bacterial infections by killing the bacterial cells. Examine the molecular structures below and propose a likely mechanism for the function of sulfanilamide. (4pts) HO, O O=S=0 NH2 NH2 NH2 Sulfanilamide DARA cataluzer
All of the following methods of actions are bacteriostatic except: competitive inhibition with folic acid synthesis inhibition of protein synthesis inhibition of cell wall synthesis competitive inhibition with DNA gyrase
Organic Chemistry 3) Propose a stepwise mechanism for the following transformations- NaOEt 0 EtOH H OET + CI Et 4) Propose a stepwise mechanism for the following transformations H2O+ HO.O. OH shi Ho Hogan
Organic Chemistry Synthesis. Using any necessary reagents. Propose a synthesis for this compound compound.
Organic Chemistry Post Lab Questions for the Synthesis of Luminol synthesis of Luminol from 3-nitrophthalic acid and hydrazide 1. A. Draw a well-labeled diagram which shows the singlet state, singlet excited state and the triplet state in a energy level diagram. Show the spin of electrons in each of these states. B. Show transitions in your diagram and label the radiative processes as either phosphorescence or fluorescence C. Discuss which of these are "allowed "transitions and which are "forbidden" transitions....