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Fittoniya [83]
3 years ago
14

I need help with chemical formulas​

Chemistry
1 answer:
pochemuha3 years ago
7 0

Answer:

Which one?

Explanation:

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Actual value= -273 Experimental value= -274
Maurinko [17]

Answer:

<h2><u><em>When measuring data, the result often varies from the true value. Error can arise due to many different reasons that are often related to human error, but can also be due to estimations and limitations of devices used in measurement. Regardless, in cases such as these, it can be valuable to calculate the percentage error. The computation of percentage error involves the use of the absolute error, which is simply the difference between the observed and the true value.</em></u></h2>

Explanation:

4 0
3 years ago
2NO + 3MnO2 + 4H â 2NO3- + 3Mn2 + 2H2O For the above redox reaction, assign oxidation numbers and use them to identify the eleme
mixer [17]

Answer:

Manganese decreases from 4+ to 2+ (reduced and oxidizing agent) and nitrogen increases from 2+ to 5+ (oxidized and reducing agent).

Explanation:

Hello there!

In this case, according to the given redox reaction, we rewrite it as a convenient first step:

2NO + 3MnO_2 + 4H^+ \rightarrow 2NO_3^- + 3Mn^{2+} + 2H_2O

Next, we assign the oxidation numbers as follows:

2N^{2+}O^{2-} + 3Mn^{4+}O^{-2}_2 + 4H^+ \rightarrow 2(N^{5+}O^{2-}_3)^- + 3Mn^{2+} + 2H^+_2O^{2-}

Thus, we can see that both manganese and nitrogen undergo a change in their oxidation number, the former decreases from 4+ to 2+ (reduced and oxidizing agent) and the latter increases from 2+ to 5+ (oxidized and reducing agent).

Regards!

4 0
3 years ago
The aldol reaction is catalyzed by acid as well as base. What is the reactive nucleophile in the acid-catalyzed aldol reaction
svp [43]

Answer:

The reactive nucleophile is Ketone.

Explanation:

In organic chemistry, The process of acid - catalyzed aldol condensation starts from when ketone (or any aldehyde) is converted to an -enol, after which it attacks another ketone/aldehyde that has already been activated by parbonyl oxygen protonation.

The process of this is that first of all the ketone undergoes tautomerization to form -enol. Thereafter, the other carbonyl will undergo protonation which makes the carbon activated towards attack. Now, the nucleophilic enol will be added to the carbonyl in a [1,2]-addition reaction and we will now use deprotonation to obtain the neutral Aldol product.

Now, since only the ketone can produce an -enol, thus it is the nucleophile as aldehydes are better electrophiles

4 0
3 years ago
Help please fast will mark as Brainliest
wlad13 [49]

Answer:

The answer is 2i on right hand side.

Explanation:

We should star by checking the equation from right.

First we check how many Zn r there in left hand side. Which is 1. Let us check how many Znr there in right hand side, there is 1.So Zn is balanced, and don't worry about Znplus2 on right hand side it is just the ions not how many zinc r there.

Now let us check how many I are there left hand side. Which is 2. Now how many I are there in right hand side? Only 1.

So we put 2 behind I.

Now there r 2 I on both sides.

Its simple actually.

3 0
3 years ago
Read 2 more answers
Choose the best answer please .
STALIN [3.7K]

Answer:

B

Explanation:

3 0
3 years ago
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