Consider the diagram below
1 answer:
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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.
The concentration of diluted solution is 0.16 M
<u>Explanation:</u>
As, the number of moles of diluted solution and concentrated solution will be same.
So, the equation used to calculate concentration will be:
where,
are the molarity and volume of the concentrated HCl solution
are the molarity and volume of diluted HCl solution
We are given:
Putting values in above equation, we get:
Hence, the concentration of diluted solution is 0.16 M
Answer:
B. The carbons on either side of the double bond are Pointed in opposite directions
