Answer:200/3 M which is approximately equal to 66.6667 M
Explanation:Molarity is defined as the number of moles of solute per liter of solution.
It can be calculated as follows:
We are given that:
number of moles of solute = 8 moles
volume of solution = 120 ml = 0.12 liters
Substitute with the givens in the above equation to get the molarity as follows:
molarity =
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The 4 main one are Iron, oxygen, silicon, and magnesium<span />
The enthalpy of combustion of 1 mole of benzene is 3169 kJ/mol .
The first step in answering this question is to obtain the balanced thermochemical equation of the reaction. The thermochemical equation shows the amount of heat lost or gained.
The thermochemical equation for the combustion of benzene is;
2 C6H6(l) + 15 O2(g) → 12 CO2(g) + 6 H2O(g) ΔrH° = -3169 kJ/mol
We can see that 1 mole of benzene releases about 3169 kJ/mol of heat.
Learn more: brainly.com/question/13164491
To determine the number of moles of carbon dioxide that is produced, we need to know the reaction of the process. For the reaction of HCl and sodium carbonate, the balanced chemical equation would be expressed as:
2HCl + Na2CO3 = 2NaCl + H2O + CO2
From the initial amount given of sodium carbonate and the relation of the substances from the balanced reaction, we calculate the moles of carbon dioxide as follows:
0.2 moles Na2Co3 ( 1 mol CO2 / 1 mol Na2Co3 ) = 0.2 moles CO2
Therefore, the amount in moles of carbon dioxide that is produced from 0.2 moles sodium carbonate would be 0.2 moles as well.
Answer:
The structure with the ring flipped is the most stable
Explanation:
We have the trans 1,2 - dimethylcyclohexane. With the wedge/dash structure we could not figure is this form is stable (If we do a comparison with the cis structure). But when we do a chair structure and ring flipped structure, this is easier to look.
The picture attached shows the structures, they are labeled as 1, 2 and 3, according to this problem.
In the chair structure, according to the picture below, you can see that both methyls are heading in the axial positions of the ring (One facing upward and the other downward). This is pretty stable, however, when the methyls are in those positions, the methyl position 1, can undergoes an 1,3 diaxial interactions with the hydrogens atoms (They are not drawn, but still are there), so this interaction makes this structure a little less stable that it can be.
On the other side, the ring flipped structure, we can see that both methyls are in the equatorials positions of the ring, and in these positions, it can avoid the 1,4 diaxial interactions with the hydrogens atoms, making this structure the most stable structure.
Hope this helps
