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3 years ago

About how long does it take for the reaction to reach equilibrium in this concentration versus time graph?

Chemistry

1 answer:

densk [106]3 years ago

5 0

Answer:

D- 4.5 Seconds

Explanation:

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Which of the following is a double replacement reaction? Ca(OH)2 + H2SO4 → CaSO4 + 2H2O CH4 + 2O2 → CO2 + 2H2O 8Fe + S8 → 8FeS Z

abruzzese [7]

That would be the first option Ca(OH)2 + H2SO4 → CaSO4 + 2H2O.

The Ca replaces the H2 in H2SO4, and the H2 replaces the Ca is Ca(OH)2.

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3 years ago

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1. The molar mass of BeF2

oksano4ka [1.4K]

Answer:

47.01 g/mol is molar mass

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3 years ago

How many grams of material is lost in the aqueous phase if two extractions are carried out on 100 mL of a 5% (m/v) aqueous solut

san4es73 [151]

Answer:

4.94g of material

Explanation:

Partition coefficient (Kp) of a substance is defined as the ratio between concentration of organic solution and aqueous solution, that is:

Kp = 8 = Concentration in Ethyl acetate / Concentration in water

100mL of a 5% solution contains 5g of material in 100mL of water. Thus:

8 = X / 100mL / (5g-X) / 100mL

Where X is the amount of material in grams that comes to the organic phase.

8 = X / 100mL / (5g-X) / 100mL

8 = 100X / (500-100X)

4000 - 800X = 100X

4000 = 900X

4.44g = X

Thus, in the first extraction you will lost 4.44g of material from the aqueous phase.

And will remain 5g-4.44g = 0.56g.

In the second extraction:

8 = X / 100mL / (0.56g-X) / 100mL

8 = 100X / (56-100X)

448 - 800X = 100X

448 = 900X

0.50g = X

In the second extraction, you will extract 0.50g of material

Thus, after the two extraction you will lost:

4.44g + 0.50g = 4.94g of material

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3 years ago

Soaps feel slippery on our hands because they dissolve the oil on our skin, decreasing friction.This is because soap contains

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The best answer to this question is D.a base

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3 years ago

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A variation of the acetamidomalonate synthesis can be used to synthesize serine. The process involves the following steps: Ethox

Alex73 [517]

Answer:

See detailed mechanism in the image attached

Explanation:

The mechanism shown in detail below is the synthesis of serine in steps.

The first step is the attack of the ethoxide ion base on the diethyl acetamidomalonate substrate giving the enolate and formaldehyde.

The second step is the protonation of the oxyanion from (1) above to form an alcohol as shown.

Acid hydrolysis of the alcohol formed in (3) above yields a tetrahedral intermediate, a dicarboxyamino alcohol.

Decarboxylation of this dicarboxyamino alcohol yields serine, the final product as shown in the image attached.

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3 years ago