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OLEGan [10]
3 years ago
7

Urea (CH4N2O) is a common fertilizer that can be synthesized by the reaction of ammonia (NH3) with carbon dioxide as follows: 2N

H3(aq) + CO2(aq) --> CH4N2O(aq) + H2O(l) In an industrial synthesis of urea, a chemist combines 122.5kg of ammonia with 211.4kg of carbon dioxide and obtains 170.3kg of urea. Determine the limiting reactant. (express your answer as a chemical formula) Determine the theoretical yield of urea. (express using four significant figures) m=___________kg Determine the percent yield for the reaction. (express your answer using three significant figures)
Chemistry
1 answer:
Gnesinka [82]3 years ago
3 0

Answer:

NH3 is the limiting reactant

The theoretical yield is 216.0 kg urea

The % for this reaction is 78.8 %

Explanation:

<u>Step 1:</u> Data given

Mass of ammonia = 122.5 kg

Mass of carbon dioxide = 211.4 kg

Mass of urea produced = 170.3 kg

Molar mass of ammnoia = 17.031 g/mol

Molar mass of carbon dioxide = 44.01 g/mol

Moalr mass of urea = 60.06 g/mol

<u>Step 2:</u> The balanced equation

2NH3(aq) + CO2(aq) --> CH4N2O(aq) + H2O(l)

<u>Step 3:</u> Calculate moles of NH3

Number of moles = mass / Molar mass

Moles NH3 = 122500 grams / 17.031 g/mol

Moles NH3 = 7192.77 moles

<u>Step 4:</u> Calculate moles of CO2

Moles CO2 = 211400 / 44.01 g/mol

Moles CO2 = 4803.45 moles

<u>Step 5</u>: Calculate limiting reactant

For 2 moles NH3 consumed, we need 1 moles of CO2 to produce 1 mole urea and 1 mole H2O

NH3 is the limiting reactant. It will completely be consumed (7192.77 moles).

CO2 is in excess. There will be consumed 7192.77/2 = 3596.4 moles

There will remain 4803.45 - 3596.4 = 1207.05 moles of CO2

<u>Step 6:</u> Calculate moles of urea produced:

For 2 moles NH3 consumed, we need 1 moles of CO2 to produce 1 mole urea and 1 mole H2O

For 7192.77 moles of NH3, we have 3596.4 moles of urea produced

<u>Step 7: </u>Calculate mass of urea

Mass urea = moles urea * molar mass urea

Mass urea = 3596.4 moles * 60.06 g/mol

Mass urea = 216000 grams = 216 kg = theoretical yield

<u>Step 8</u>: Calculate % yield

% yield = (actual yield / theoretical yield)*100%

% yield = (170.3 / 216) *100% = 78.8%

The % for this reaction is 78.8 %

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What is the standard electrode potential for a galvanic cell constructed in the appropriate way from these two half-cells?
____ [38]

E

θ

Cell

=

+

2.115

l

V

Cathode

Mg

2

+

/

Mg

Anode

Ni

2

+

/

Ni

Explanation:

Look up the reduction potential for each cell in question on a table of standard electrode potential like this one from Chemistry LibreTexts. [1]

Mg

2

+

(

a

q

)

+

2

l

e

−

→

Mg

(

s

)

−

E

θ

=

−

2.372

l

V

Ni

2

+

(

a

q

)

+

2

l

e

−

→

Ni

(

s

)

−

E

θ

=

−

0.257

l

V

The standard reduction potential

E

θ

resembles the electrode's strength as an oxidizing agent and equivalently its tendency to get reduced. The reduction potential of a Platinum-Hydrogen Electrode under standard conditions (

298

l

K

,

1.00

l

kPa

) is defined as

0

l

V

for reference. [2]

A cell with a high reduction potential indicates a strong oxidizing agent- vice versa for a cell with low reduction potentials.

Two half cells connected with an external circuit and a salt bridge make a galvanic cell; the half-cell with the higher

E

θ

and thus higher likelihood to be reduced will experience reduction and act as the cathode, whereas the half-cell with a lower

E

θ

will experience oxidation and act the anode.

E

θ

(

Ni

2

+

/

Ni

)

>

E

θ

(

Mg

2

+

/

Mg

)

Therefore in this galvanic cell, the

Ni

2

+

/

Ni

half-cell will experience reduction and act as the cathode and the

Mg

2

+

/

Mg

the anode.

The standard cell potential of a galvanic cell equals the standard reduction potential of the cathode minus that of the anode. That is:

E

θ

cell

=

E

θ

(

Cathode

)

−

E

θ

(

Anode

)

E

θ

cell

=

−

0.257

−

(

−

2.372

)

E

θ

cell

=

+

2.115

Indicating that connecting the two cells will generate a potential difference of

+

2.115

l

V

across the two cells.

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