Answer:
Volume = 72.7272
Explanation:
if only pressure and volume change, then we can do some simple math to find the answer.
2 x 10 ^ 6 times 1 x 10 ^-5 = 20
pressure and volume must equal 20
20 = 0.275 x volume
20 / 0.275 = new volume
I don't remember significant digits but your volume is 72.72727272 just repeated
One separation technique to be used is the paper chromatography. This works by separating the components of the mixture through the difference of their concentrations. There is a stationary phase and the mobile phase, which flows through the stationary phase. The components travel at different rates and is usually signified by the colors. If more than one color would appear, that means that the dye is a mixture.
Answer:
144g of H₂O
Explanation:
3NH₄ClO₄(s) + 3Al → Al₂O₃(s) + AlCl₃(s) + 3NO(g) + 6H₂O(g)
From the equation:
3 moles of NH₄ClO₄ produced 6 moles of H₂O
4 moles of NH₄ClO₄ produced ? moles of H₂O
(4 ₓ 6)/3 =
= 8 moles of H₂O
1 mole of H₂O = (1 × 2) + 16 = 18g (The Relative Molecular mass of H₂O)
8 moles of H₂O = ?
Therefore 8 × 18 = 144g
=144g of H₂O
Answer:
The molecular equation for the reaction betweensodium carbonate and sulfuric acid is: 1. Na2CO3(aq)+H2SO4(aq)→Na2SO4(aq)+CO2(g)+H2O(l) N a 2 C O 3 ( a q ) + H 2 S O 4 ( a q ) → N a 2 S O 4 ( a q ) + C O 2 ( g ) + H 2 O ( l ) .
Explanation:
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.