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Gnoma [55]
2 years ago
5

NEED HELP ASAP! Write a statement explaining your claim about whether or not the equation is correctly balanced.

Chemistry
2 answers:
cupoosta [38]2 years ago
8 0

Answer:

I think that it it correctly balanced that is my opinion and, because  the way it is set up, that the answer will tell you weather or not it is correctly balanced or not.

Kisachek [45]2 years ago
4 0

Evaluating the number of atoms of each element on the product and reactant side, we can conclude that the student's equation isn't balanced.

<u>Given the chemical reaction</u> :

Al_{4}C_{3} + 6H_{2}O ---> 3CH_{4} + 4Al(OH)_{3}

For a balanced equation, the number of atoms of each element in the product side must be equal to that on the reactant side.

<u>Number of hydrogen</u> :

Reactant side = (6 × 2) = 12

Product side = (6 × 2) + (6 × 2) = 12 + 24 = 24

<em>Product side ≠ reactant side</em> ; Hence, the equation isn't balanced

<u>The balanced equation for the reaction goes thus</u> :

Al_{4}C_{3} + 12H_{2}O ---> 3CH_{4} + 4Al(OH)_{3}

<u>Reactant side</u> :

Al = 4

H = (12 × 2) = 24

O = 12

C = 3

<u>Product side</u> :

H = (6 × 2) + (6 × 2) = 12 + 24 = 24

Al = 4

O = 4 × 3 = 12

C = 3

Therefore, the student's equation isn't balanced, the balanced version of the equation has been given .

Learn more :brainly.com/question/2720947

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Answer:

See details below

Explanation:

The balanced reaction equation is given below:

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8 0
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Let's say that you were given the following
mezya [45]

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Explanation:

We're going to use Boyles law to answer the question.

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Hope it helps:)

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Neopentyl alcohol, (ch3)3cch2oh, cannot be dehydrated to an alkene without rearrangement. what is the chief product of dehydrati
emmainna [20.7K]

Dehydration is removal of water.

In alcohols dehydration is α-β elimination or 1,2 elimination, it means the hydroxyl group will be removed from α-carbon while the hydrogen will be removed from near by carbon.

In case of neopentyl alcohol there is no β hydrogen present on the β carbon [as shown in figure].

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