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Kamila [148]
3 years ago
7

Need help answering the question at the bottom of the text

Chemistry
1 answer:
Rasek [7]3 years ago
7 0

Answer:

You Need to put in the picture

Explanation:

I cant see it

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NiS2(s) + O2(g) --> NiO(s) + SO2(g) When 11.2 g of NiS2 react with 5.43 g of O2, 4.86 g of NiO are obtained. The theoretical
makkiz [27]

Answer:

1. The theoretical yield of NiO is 5.09g.

2. O2 is the limiting reactant.

3. The percentage yield of NiO is 95.5%

Explanation:

Step 1:

The balanced equation for the reaction is given below:

2NiS2(s) + 5O2(g) —> 2NiO(s) + 4SO2(g)

Step 2:

Determination of the masses of NiS2 and O2 that reacted and the mass of NiO produced from the balanced equation. This is illustrated below below:

Molar mass of NiS2 = 59 + (32x2) = 123g/mol

Mass of NiS2 from the balanced equation = 2 x 123 = 246g

Molar mass of o3= 16x2 = 32g/mol

Mass of O2 from the balanced equation = 5 x 32 = 160g

Molar mass of NiO = 59 + 16 = 75g/mol

Mass of NiO from the balanced equation = 2 x 75 = 150g

Summary:

From the balanced equation above, 246g of NiS2 reacted with 160g of O2 to produce 150g of NiO

Step 3:

Determination of the limiting reactant. This can be obtain as follow:

From the balanced equation above, 246g of NiS2 reacted with 160g of O2.

Therefore, 11.2g of NiS2 will react with = (11.2 x 160)/246 = 7.28g of O2.

From the above calculation, we can see that it will take a higher mass of O2 i.e 7.28g than what was given i.e 5.43g to react completely with 11.2g of NiS2.

Therefore, O2 is the limiting reactant and NiS2 is the excess reactant.

1. Determination of the theoretical yield of NiO.

In this case, the limiting reactant will be used as all of it is consumed in the reaction. The limiting reactant is O2.

From the balanced equation above, 160g of O2 reacted to produce 150g of NiO.

Therefore, 5.43g of O2 will react to produce = (5.43 x 150)/160 = 5.09g of NiO.

Therefore, the theoretical yield of NiO is 5.09g.

2. The limiting reactant is O2. Please review step 3 above for explanation.

3. Determination of the percentage yield of NiO. This is illustrated below:

Actual yield of NiO = 4.86g

Theoretical yield of NiO = 5.09g

Percentage yield =..?

Percentage yield = Actual yield /Theoretical yield x 100

Percentage yield = 4.86/5.09 x 100

Percentage yield of NiO = 95.5%

3 0
3 years ago
What are the similarities between the adrenal hormone cortisone and the synthetic corticoid prednisone?
vaieri [72.5K]

Answer:

Options a,b, c and d are correct

Explanation:

From the diagram attached in the picture below, They both have steroid nucleus since they have functional groups (such as the methyl and the ketone groups) that are spatially attached. It can also be deduced that both structures have three (3) ketone groups (CO/C=O), two (2) methyl groups (CH₃) and two (2) hydroxyl groups (OH). Hence, options a, b,c and d are correct.

However, cortisone has one (1) double bond while prednisone has two (2) double bonds.

8 0
3 years ago
Helium and nickel are examples of ________. These
emmasim [6.3K]

Answer:

Elements, in turn, are pure substances—such as nickel, hydrogen, and helium—that make up all kinds of matter.

Hope This Helps!       Have A Nice Day!!

3 0
3 years ago
How are prefixes used to name compounds
Dennis_Churaev [7]

However, simple covalent compounds are generally named by using prefixes to indicate how many atoms of each element are shown in the formula. Also, the ending of the last (most negative) element is changed to -ide. The prefixes used are mono-, di-, tri-, tetra-, penta-, hexa-, and so forth.

4 0
3 years ago
Read 2 more answers
What is the angle between the phosphorus-fluorine bonds? (if there is more than one angle, pick the smallest.)
lorasvet [3.4K]

Between equatorial positions, the F-P-F angle is 120°, and between axial and equatorial positions, it is 90°.

<h3>What in chemical bonding is equatorial position?</h3>

Equatorial Organic Chemistry Illustrated Glossary. Equatorial: In cyclohexane, a bond that runs parallel to the ring's axis (i.e., it follows the chair's equator), or a group joined by such a bond. Positions A are axial, and positions E are equatorial.

<h3>Why do equatorial positions have greater stability?</h3>

As was said in the preceding section, the equilibrium favors the more stable conformer because the chair conformation, in which the methyl group is equatorial, lowers steric repulsion. All monosubstituted cyclohexanes share this property.

To know more about equatorial positions visit:

brainly.com/question/24168112

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5 0
2 years ago
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