if your serious about this question then it is 5
Answer:
83.20 g of Na3PO4
Explanation:
1 mole of Na3PO4 contains 3 moles of Na+.
Mole of Na ion to be prepared = Molarity x volume
= 0.700 x 725/1000
= 0.5075 mole
If 1 mole of Na3PO4 contains 3 moles of Na ion, then 0.5075 Na ion will be contained in:
0.5075/3 x 1 = 0.1692 mole of Na3PO4
mole of Na3PO4 = mass/molar mass = 0.1692
Hence, mass of Na3PO4 = 0.1692 x molar mass
= 0.1692 x 163.94
= 83.20 g.
83.20 g of Na3PO4 will be needed.
<u>Answer:</u> The molality of magnesium chloride is 1.58 m
<u>Explanation:</u>
To calculate the molality of solution, we use the equation:

Where,
= Given mass of solute (magnesium chloride) = 75.0
= Molar mass of solute (magnesium chloride) = 95.21 g/mol
= Mass of solvent = 500.0 g
Putting values in above equation, we get:

Hence, the molality of magnesium chloride is 1.58 m
Answer:
Propane
Explanation:
From the question given, we were told that 0.1240 kg of propane reacted with excess oxygen to produce 0.3110kg of carbon dioxide.
Since the reaction took place in the presence of excess oxygen, therefore, propane is the limiting reactant as all of it is used up in the presence of excess oxygen.
Answer:
See explanation and picture below
Explanation:
First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.
In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.
In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.