Water

4. How many grams of ammonium carbonate are needed to decompose in order to produce

Thepotemich [5.8K]

Answer:

14.23g of (NH4)2CO3

Explanation:

We'll begin by writing the balanced equation for the reaction.

(NH4)2CO3 –> (NH4)2O + CO2

Next,, we shall determine the mass of (NH4)2CO3 that decomposed and the mass of CO2 produced from the balanced equation. This is illustrated below:

Molar mass of (NH4)2CO3 = 2[14+(4x1)] + 12 + (16x3)

= 2[14 +4] + 12 + 48

= 2[18] + 60 = 96g/mol

Mass of (NH4)2CO3 from the balanced equation = 1 x 96 = 96g

Molar mass of CO2 = 12 + (2x16) = 44g/mol

Mass of CO2 from the balanced equation = 1 x 44 = 44g.

Summary:

From the balanced equation above,

96g of (NH4)2CO3 decomposed to produce 44g of CO2.

Finally, we can determine the mass of (NH4)2CO3 that decomposed to produce 6.52g of CO2 as follow:

From the balanced equation above,

96g of (NH4)2CO3 decomposed to produce 44g of CO2.

Therefore, Xg of (NH4)2CO3 will decompose to produce 6.52g of CO2 i.e

Xg of (NH4)2CO3 = (96 x 6.52)/44

Xg of (NH4)2CO3 = 14.23g

Therefore, 14.23g of (NH4)2CO3 is needed to produce 6.52g of CO2.

4 0

3 years ago

Which term best describes the rate at which global erosion takes place

dlinn [17]

The correct answer is slow

5 0

3 years ago

What is the main purpose of the second paragraph?

Svetlanka [38]

To explain your first paragraph which includes your thesis. The second paragrph supports your first pragraph

5 0

3 years ago

Name a possible product of this reaction in the presence of ether and AlCl3: methylbenzene + 1-chlorodecane.a. 1-methyl-2-decylb

Vikki [24]

Answer:

None of these

Explanation:

Friedel–Craft reaction is a reaction involves the attachment of substituents to the benzene ring.

Mechanism of the reaction of methylbenzene with 1-chlorodecane in the presence of ether and aluminum chloride :

Step -1 : Generation of stable carbocation.

Aluminium chloride acts as Lewis acid which removes the chloride ion from the alkyl halide forming carbocation. The primary carbocation thus formed gets rearranged to secondary primary carbocation which is more stable due to hyperconjugation.

Step-2: Attack of the ring to the carbocation

The pi electrons of the ring behave as a nucleophile and attacks the carbocation. Since, the group attached on the benzene is methyl (+R effect) , the attack is from the ortho and the para positions. Para product is more stable due to less steric hinderance.

The product formed is shown in mechanism does not mention in any of the options.

So, None of these is the answer