Answer:
The two molecules of acetyl-CoA that are produced from a molecule of glucose goes through two turn in the citric acid cycle, one for each molecule of acetyl-CoA.
Explanation:
Glycolysis the process by which a molecule of glucose is broken down in a series of steps to yield two molecules of pyruvate. The overall equation for the reactions of glycolsis is given below:
Glucose + 2NAD+ ----> 2 Pyruvate + 2NADH + 2H⁺
Each of the two pyruvate molecules produced from glucose breakdown is further oxidized to two molecules of acetyl-CoA and CO₂ each.
2 Pyruvate ----> 2 AcetylCoA + 2CO₂
Each of the acetyl-CoA molecule then enters the citric acid cycle for its oxidation. In each turn of the cycle, one acetyl group enters as acetyl-CoA and two molecules of CO₂ leave.
No a molecule is 2 different atoms bond
For example, ionic compounds, which are very polar, are often soluble in the polar solvent water. Nonpolar substances are likely to dissolve in nonpolar solvents. For example, nonpolar molecular substances are likely to dissolve in hexane, a common nonpolar solvent.
Answer:
Four possible isomers (1–4) for the natural product essramycin. The structure of compound 1 was attributed to essramycin by 1H NMR, 13C NMR, HMBC, HRMS, and IR experiments.
Explanation:
Three synthetic routes were used to prepare all four compounds (Figure 2A). All three reactions utilize 2-(5-amino-4H-1,2,4-triazol-3-yl)-1-phenylethanone (5) as the precursor, whereas each uses different esters (6–8) to construct the pyrimidinone ring. Isomer 1 was prepared by reaction A, which used triazole 5 and ethyl acetoacetate (6) in acetic acid. This was the reaction used in syntheses of essramycin by the Cooper and Moody laboratories.3,4 Reaction B produced compound 2 (minor product) and compound 3 (major product), which were separated chromatographically. This reaction allowed reagent 5 to react with ethyl 3-ethoxy-2-butenoate (7) in the presence of sodium in methanol, under reflux for 24 h. Compound 4 was prepared by reaction C, which was obtained by reflux of 5 and methyl 2-butynoate (8) in n-butanol.