Answer:
electrical
Explanation:
With electrical energy, it's helpful to think of an on/off switch. When the switch is off, the electrical energy is stored as potential energy. When the switch is on, electrical energy is being used as kinetic energy.
5. Eubacteria
6. Plantae
7. Animalia
8. Protist (technically not a kingdom)
9. Archaebacteria
10. Fungi
Answer:
at the beginning:
pH = 0.745
Explanation:
HCl is a strong acid, so:
0.18 M 0.18 0.18.....equilibrium
before base is added:
∴ [ H3O+ ] ≅ <em>C </em>HCl = 0.18 M
⇒ pH = - Log [ H3O+ ] = - Log ( 0.18 )
⇒ pH = 0.745
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.