Answer:4)Wind energy can harm migrating birds.
Explanation:
Because the valence shell of gases wants to become full
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.
Answer:
Explanation:
H2SO4 let S be x
2(1) + x + 4(-2) = 0
2 + x - 8 = 0
x - 6 = 0
x = 6
For H2S7O8 let S be x
2(1) + 7(x) + 8(-2) = 0
2 + 7x - 16 = 0
7x - 14 = 0
7x = 14
x = 14/7
x = 2
:- H2SO4 as the larger percentage