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mestny [16]
4 years ago
13

Which of the following is not a result when a change to an equilibrium system is applied? (2 points)

Chemistry
2 answers:
Ray Of Light [21]4 years ago
8 0
It should be increasing the rate of the forward reaction will cause a shift to the left because the external stress, which is the increase in rate, will cause the reaction to be unbalanced, and to reach equilibrium it needs to shift to the right.
Ksju [112]4 years ago
6 0

Answer: Option (2) is the correct answer.

Explanation:

According to LeChatelier principle, any change in the equilibrium of a chemical reaction will result in shifting of equilibrium which is opposing the change.

Therefore, when we increase the rate of the reverse reaction that is, we move towards left side then this will actually cause a shift to the right hand side which is opposing the change.

Thus, we can conclude that increasing the rate of the reverse reaction will cause a shift to the left is not a result when a change to an equilibrium system is applied.

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Help me plsss
Yuki888 [10]

Answer:

8.34

Explanation:

1) how much moles of NH₃ are in the reaction;

2) how much moles of H₂ are in the reaction;

3)  the required mass of the H₂.

all the details are in the attachment; the answer is marked with red colour.

Note1: M(NH₃) - molar mass of the NH₃, constant; M(H₂) - the molar mass of the H₂, constant; ν(NH₃) - quantity of NH₃; ν(H₂) - quantity of H₂.

Note2: the suggested solution is not the shortest one.

8 0
3 years ago
The SN1 reaction yields Entry field with incorrect answer two (number) products. This is because ______________________. Entry f
vagabundo [1.1K]

Answer:

Four substitution products are obtained. The carbocation that forms can react with either nucleophile (H2O or CH3OH) from either the top or bottom side of the molecule

Explanation:

An SN1 reaction usually involves the formation of a carbocation in the slow rate determining step. This carbocation is now attacked by a nucleophile in a subsequent fast step to give the desired product.

However, the product is obtained as a racemic mixture because the nucleophile may attack from the top or bottom of the carbocation hence both attacks are equally probable.

The attacking nucleophile in this case may be water or CH3OH

4 0
4 years ago
How can you get unconscious
sesenic [268]
When sudden changes occurs in the body. lack of blood flow in the brain
6 0
3 years ago
W
natali 33 [55]

Answer:

I would say is B but I do t really know

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2 methylhaxanal structure
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Answer:

Look at the photo.

Hope this helps!

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