Certain gases in the atmosphere trap heat on Earth.
1 answer:
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Answer:
a) The relationship at equivalence is that 1 mole of phosphoric acid will need three moles of sodium hydroxide.
b) 0.0035 mole
c) 0.166 M
Explanation:
Phosphoric acid is tripotic because it has 3 acidic hydrogen atom surrounding it.
The equation of the reaction is expressed as:
1 mole 3 mole
The relationship at equivalence is that 1 mole of phosphoric acid will need three moles of sodium hydroxide.
b) if 10.00 mL of a phosphoric acid solution required the addition of 17.50 mL of a 0.200 M NaOH(aq) to reach the endpoint; Then the molarity of the solution is calculated as follows
10 ml 17.50 ml
(x) M 0.200 M
Molarity =
= 0.0035 mole
c) What was the molar concentration of phosphoric acid in the original stock solution?
By stoichiometry, converting moles of NaOH to H₃PO₄; we have
=
= 0.00166 mole of H₃PO₄
Using the molarity equation to determine the molar concentration of phosphoric acid in the original stock solution; we have:
Molar Concentration =
Molar Concentration =
Molar Concentration = 0.166 M
∴ the molar concentration of phosphoric acid in the original stock solution = 0.166 M
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.
