10. Isolation of a pure sample of the third product, which has been determined to be an isomer of the major and minor products, gives the following 13C NMR data. Determine the structure of this product. 2 points

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.

metals are good conductor of electricity. it has free electrons on their surface. according to electron pool theory, each atom present in a metal crystal losses all of its valence electron and as a result a pool of free is form. these pool of electrons are free to move and   conduct electricity easily   while making metal as good conductor.

the correct answer is a. the ability of electrons to flow throughout the metal.

if it's not useful, feel free to report for mistake in answer.