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harkovskaia [24]
3 years ago
7

Zn(s) + 2HCl(aq) mc029-1.jpg H2(g) + ZnCl2(aq) Which product is a substance that is dissolved in solution?

Chemistry
1 answer:
nexus9112 [7]3 years ago
8 0
The product that is dissolved in the solution would be the salt zinc chloride. It is a substance that is soluble in water so it should be dissolved in the solution. Also, from the reaction, the sign (aq) is written. It means that this substance is in aqueous solution.
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Answer:

<h2>belajar jangan malas malas</h2>
5 0
3 years ago
Comment Both propane and benzene are hydrocarbons. As a rule,
kozerog [31]

The enthalpy change : -196.2 kJ/mol

<h3>Further explanation  </h3>

The change in enthalpy in the formation of 1 mole of the elements is called enthalpy of formation  

The enthalpy of formation measured in standard conditions (25 ° C, 1 atm) is called the standard enthalpy of formation (ΔHf °)  

(ΔH) can be positive (endothermic = requires heat) or negative (exothermic = releasing heat)  

The value of ° H ° can be calculated from the change in enthalpy of standard formation:  

∆H ° rxn = ∑n ∆Hf ° (product) - ∑n ∆Hf ° (reactants)  

Reaction

2 H₂O₂(l)-→ 2 H₂O(l) + O₂(g)

∆H ° rxn = 2. ∆Hf ° H₂O - 2. ∆Hf °H₂O₂

\tt \Delta H_{rxn}=2.(-285.8)-2.(-187.8)\\\\\Delta H_{rxn}=-571.6+375.4=-196.2~kJ/mol\rightarrow \Delta Hf~O_2=0

5 0
3 years ago
What will be the volume of a gas sample at 331 K if its volume at 371 K is 14.8 L?
lianna [129]

Answer:

13.20 litres

Explanation:

use pascal's law of volume and temperature

8 0
3 years ago
What are compounds that react with acids and bases to make certain colors?
finlep [7]
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4 0
3 years ago
The product of the nitration reaction will have a nitro group at which position with respect to the methyl group? Group of answe
zimovet [89]

Answer:

Mostly Para

Explanation:

First, let's assume that the molecule is the toluene (A benzene with a methyl group as radical).

Now the nitration reaction is a reaction in which the nitric acid in presence of sulfuric acid, react with the benzene molecule, to introduce the nitro group into the molecule. The nitro group is a relative strong deactiviting group and is metha director, so, further reactions that occur will be in the metha position.

Now, in this case, the methyl group is a weak activating group in the molecule of benzene, and is always ortho and para director for the simple fact that this molecule (The methyl group) is a donor of electrons instead of atracting group of electrons. Therefore for these two reasons, when the nitration occurs,it will go to the ortho or para position.

Now which position will prefer to go? it's true it can go either ortho or para, however, let's use the steric hindrance principle. Although the methyl group it's not a very voluminous and big molecule, it still exerts a little steric hindrance, and the nitro group would rather go to a position where no molecule is present so it can attach easily. It's like you have two doors that lead to the same place, but in one door you have a kid in the middle and the other door is free to go, you'll rather pass by the door which is free instead of the door with the kid in the middle even though you can pass for that door too. Same thing happens here. Therefore the correct option will be mostly para.

4 0
3 years ago
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