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.
Are able to travel inside to conduct electricity
Answer:
D
We don't have a way to contain the radioactive waste produced.
Explanation
Nuclear waste is non disposable and takes millions of years to biodegrade and lose it radio activeness
Answer:
0.228 mol FeO
Explanation:
2FeS2 + 5 O2----> 2FeO + 4SO2
from reaction 5 mol 2 mol
given 0.57 mol x
x = 0.57*2/5 = 0.228 mol FeO
Here we have to draw the mechanism of the reduction reaction between benzaldehyde and sodium borodeuteride to form the corresponding alcohol.
The reducing agent sodium borodeuteride can reduce the aldehydes to its corresponding alcohol. The reaction mechanism is shown in the attached image.
The reaction mechanism can be explained as-
The sodium borodeuteride is highly ionic in nature thus it remains as Na⁺ and BD₄⁻ The deuterium atom of BD₄⁻ attack the carbonyl carbon atom and substitute one of its deuterium as shown in the figure.
One molecule of sodium borodeuteride can reduce four molecules of benzaldehyde. The polar solvent like alcohol donates the proton as shown in the mechanism.
The converted alcohol contains the deuterium atom at the -C center. Thus benzaldehyde is converted to deuteroted benzyl alcohol.
