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Nataly_w [17]
2 years ago
13

How many grams of carbon would be present in carbon monoxide that contains 2.6 grams of oxygen?

Chemistry
1 answer:
Andreas93 [3]2 years ago
6 0

Answer:

1.95g

Explanation:

Find mass in CO

Find C mass

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How does thermal energy flow?
mart [117]
My answer is....A

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6 0
3 years ago
If all other variables remain unchanged, what happens to the output force when the area of the input piston is doubled?
mars1129 [50]

Answer:

1250N

Explanation:

This question is based on pascal's Law.

So By Pascal's Law

 =  

therefore  =force on input piston =25N

                  = Force or weight on output person.

therefore after putting the values we get,

= (25x 1500)/30

    =1250N

3 0
3 years ago
How many grams of solid nickel will be plated if an aqueous nickel(II) sulfate solution is electroplated over 10.5 min with a co
Anna71 [15]

Answer:

613 mg

Explanation:

$Ni^{2+} + 2e \rightarrow Ni(s)$

Number of fargday's  $=\frac{It}{96500}$

Here, I = 9.20 A

        t = 10.5 min

          = 10.5 x 60 seconds

So, $\frac{It}{96500}$

  $=\frac{3.20 \times 10.5 \times 60}{96500}$

 = 0.0208 F

Here, 2e, 2F

2F = 1 mol of Ni

$0.0208 \ F = \frac{0.0208}{2} = 0.0104 \ mol \ Ni$

1 mol = 59 gm of Ni

0.0104 mol = 59 x0.0104 gm Ni

                    = 0.613 gm Ni

                    = (0.613 x 1000 ) mg of Ni

                    = 613 mg of Ni

3 0
3 years ago
How many cm is 0.375 ft.​
ivann1987 [24]

Answer:

11.43 cm

Explanation:

8 0
2 years ago
Read 2 more answers
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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