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Fantom [35]
3 years ago
5

What is the percent yield of either if 1.11L(d=0.7134 g/mL) is isolated from the reaction of 1.500L of C2H5OH

Chemistry
1 answer:
serg [7]3 years ago
6 0

Answer:

Percent yield of ether = 83.18%

Explanation:

Equation of the synthesis reaction of ether from ethanol is given as follows :

2 C₂H₅OH -----> C₂H₅OC₂H₅ + H₂0

Density = mass / volume

Therefore mass = density × volume

Density of ether = 0.7134 g/mL; volume of ether produced = 1.11 L = 1110 mL; Molar mass of ether = 74 g/mol

Mass of ether produced = 0.7134 g/mL × 1110 mL = 791.874 g

Density of ethanol = 0.789 g/mL; volume of ethanol = 1.50 L = 1500 mL; molar mass of ethanol = 46 g/mol

Mass of ethanol reacted = 0.789 g/mL × 1500 mL = 1183.5 g

From the equation of reaction, 2 mole of ethanol produces 1 mole of ether

Mass of 2 moles of ethanol = 2 × 46 = 92 g

Therefore, 92 g of ethanol produces 74 g of ether

1183.5 g of ethanol will produce 1183.5 × 74/92 grams of ether = 951.945 g of ether

Percent yield of ether = actual yield/theoretical yield × 100%

Actual yield of ether = 791.874 g; theoretical yield of ether = 951.945 g

Percent yield of ether = (791.874 g × 951.945 g) × 100 %

Percent yield of ether = 83.18%

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mixas84 [53]

Answer:

N, B, Be, C

Explanation:

N (Nitrogen) has 14.0067 B (Boron) has 10.81 Be (Beryllium) has 9 and C (Carbon) has 12

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2 years ago
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MissTica

Answer:

Carbon 12 and carbon 13

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Explanation:

8 0
3 years ago
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Molodets [167]
1. A
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8 0
3 years ago
Which concepts can be used to explain the difference in acidicty between ethanol and 2-fluoroethanol?
Margarita [4]

Answer:

The answer is Inductive effect

Explanation:

To determine the acidity or alkalinity of an organic compound. We have to keep in mind that the whole analysis is based on the comparison between the compounds, and we must work with the conjugated base of the molecule. Keeping in mind, the more unstable the base, the less acidic the molecule is. Thus, to determine instability, the Inductive Effect of the molecule can be used.

This type of effect occurs when atoms of different electronegativities are linked or very close in the compound. The most electronegative atom has a tendency to bring electrons close to it, thus creating a dipole. This dipole can have a stabilizing effect on the molecule, as it “relieves” the excessive charge on some occasions, better accommodating the charges.

However, in some cases, instead of chains with chlorine radicals, we may have chains with methyl radicals. This has a major impact on the inductive effect, keeping in mind that alkyl groups are electron donors.

5 0
3 years ago
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cricket20 [7]

Answer:

1=4

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Explanation:

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