Answer:
Complete ionic: .
Net ionic: .
Explanation:
Start by identifying species that exist as ions. In general, such species include:
- Soluble salts.
- Strong acids and strong bases.
All four species in this particular question are salts. However, only three of them are generally soluble in water: , , and . These three salts will exist as ions:
- Each formula unit will exist as one ion and one ion.
- Each formula unit will exist as one ion and two ions (note the subscript in the formula .)
- Each formula unit will exist as one and two ions.
On the other hand, is generally insoluble in water. This salt will not form ions.
Rewrite the original chemical equation to get the corresponding ionic equation. In this question, rewrite , , and (three soluble salts) as the corresponding ions.
Pay attention to the coefficient of each species. For example, indeed each formula unit will exist as only one ion and one ion. However, because the coefficient of in the original equation is two, alone should correspond to two ions and two ions.
Do not rewrite the salt because it is insoluble.
.
Eliminate ions that are present on both sides of this ionic equation. In this question, such ions include one unit of and two units of . Doing so will give:
.
Simplify the coefficients:
.
I’ve been having problems too honestly lol
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.
A local community needs to provide more electricity for its growing population. Currently, the community's electricity needs are met by coal-burning power plants several kilometres away. Citizens are concerned that burning more coal will produce too much air pollution.
Which of the following could be used as an alternative energy resource to help minimise air pollution in this community?
A. hydroelectric energy
B. solar energy
C. wind energy
<u>D. all of these
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