Hello!
1.00 L of a gas at STP is compressed to 473 mL. What is the new pressure of gas?
- <u><em>We have the following data:</em></u>
Vo (initial volume) = 1.00 L
V (final volume) = 473 mL → 0.473 L
Po (initial pressure) = 1 atm (pressure exerted by the atmosphere - in STP)
P (final pressure) = ? (in atm)
- <u><em>We have an isothermal transformation, that is, its temperature remains constant, if the volume of the gas in the container decreases, so its pressure increases. Applying the data to the equation Boyle-Mariotte, we have:</em></u>
<u><em>Answer: </em></u>
<u><em>The new pressure of the gas is 2.11 atm </em></u>
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Answer:
6.34917360^25g
Explanation:
It's been a while since I've done this type of problem so I'm not making any promises that its right hahaha, but I hope it helps anyway. Please let me know whether I'm right or not!
Moles of Zn: 26 / 65 = 0.4
Moles of S: 12.8 / 32 = 0.4
Molar ratio of Zn : S = 1 : 1
Empircal formula: ZnS
The answer is C
Answer:
The answer is Relative plenitude alludes to the amount of a specific isotope is available in a given measure of test.
Explanation:
The 'relative plenitude' of an isotope implies the level of that specific isotope that happens in nature. Most components are comprised of a blend of isotopes. The total of the rates of the particular isotopes must indicate 100%. The relative nuclear mass is the weighted normal of the isotopic masses. The percent plenitude of every sort of sweets reveals to you what number of every sort of Aufbau there are in each 100 CANDIES. Percent wealth is additionally relative plenitude. This is only a method for giving us a photo on which kind exists all the more every now and again.
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.
