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Akimi4 [234]
3 years ago
6

What is the mass of 1 mole in ZnCl2

Chemistry
1 answer:
DENIUS [597]3 years ago
4 0

Answer:

136.286 g/mol

Explanation:

good luck

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What would you need to lower to change a gas to a liquid
IrinaVladis [17]

The temperature or the average kinetic energy of the molecules

5 0
3 years ago
2c4H10 +13O2 —>8CO2+10H2O to find how many moles of oxygen would react with 4.3 mol C4H10
Elena-2011 [213]

Answer:

\large\boxed{\text{28 mol of O$_{2}$}}

Explanation:

             2C₄H₁₀ + 13O₂ ⟶ 8CO₂ + 10H₂O

n/mol:      4.3  

13 mol of O₂ react with 2 mol of 2C₄H₁₀

\text{Moles of O}_{2} = \text{4.3 mol C$_{4}$H$_{10}$} \times \dfrac{\text{13 mol O}_{2}}{\text{2 mol C$_{4}$H$_{10}$}} = \textbf{28 mol O}_{2}\\\\\text{The reaction requires $\large\boxed{\textbf{28 mol of O$_{2}$}}$}

5 0
3 years ago
Which statements describe how heat flows in foil? Check all that apply. Heat flows in all directions. Heat flows from left to ri
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Answer:

A D F

Explanation:

Its right but its not in order But its A D and F

3 0
2 years ago
In comparison to an atom of F-19 in the ground state, an atom of C-12 in the ground state has(1) three fewer neutrons
mel-nik [20]
(2) three fewer valence electrons is your answer.
6 0
3 years ago
10. Isolation of a pure sample of the third product, which has been determined to be an isomer of the major and minor products,
Ymorist [56]

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.

7 0
3 years ago
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