We can store the copper sulphate solution in alumiun container, if cover on alumiun is present.
<h3>Can you store cuso4 in an aluminum container?</h3>
Aluminium is more reactive than copper so the Aluminium will displace copper sulphate from its solution by reacting with it but if there is cover on the aluminium then the alumium can't react with copper.
So we can store the copper sulphate solution in alumiun container.
Learn more about container here: brainly.com/question/11459708
I dont know what subject is this
It means that the fit and well adjusted ones thrive and "make it", and the weak ones that can't adapt die.
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Answer:</h3>
B) 4H₂(g) + O₂(g) ⟶ 2H₂O(l)
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Explanation:</h3>
- Chemical reactions occur when compounds or elements combine to form new compounds or other elements.
- Chemical reactions may be classified into various types which include synthesis reactions, replacement reaction, decomposition reactions, and precipitation reactions among others.
- In our case, we were supposed to identify a synthesis reaction.
- Thus, we need to know what is a synthesis reaction.
- A synthesis reaction is a reaction that occurs when two elements or small compounds combine to generate a large compound.
- In this case, B is the choice that shows a synthesis reaction where hydrogen gas combines with oxygen gas to yield water.
Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.
Discussion:
1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.
2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.
3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.
4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.
Learn more about carbonyl here:
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