Answer:
Percent by mass of water is 56%
Explanation:
First of all calculate the mass of hydrated compound as,
Mass of Sodium = Na × 2 = 22.99 × 1 = 45.98 g
Mass of Sulfur = S × 1 = 32.06 × 1 = 32.06 g
Mass of Oxygen = O × 14 = 16 × 14 = 224 g
Mass of Hydrogen = H × 20 = 1.01 × 20 = 20.2 g
Mass of Na₂S0₄.10H₂O = 322.24 g
Secondly, calculate mass of water present in hydrated compound. For this one should look for the coefficient present before H₂O in molecular formula of hydrated compound. In this case the coefficient is 10, so the mass of water is...
Mass of water = 10 × 18.02
Mass of water = 180.2 g
Now, we will apply following formula to find percent of water in hydrated compound,
%H₂O = Mass of H₂O / Mass of Hydrated Compound × 100
Putting values,
%H₂O = 180.2 g / 322.24 g × 100
%H₂O = 55.92 % ≈ 56%
Answer:
17
Explanation:
Don't mind the random letters
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Non polar covalent bond. The Cl's electronegativity is the same since it's the same atom. Therefore, they will be nonpolar
Its an element Im pretty sure
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.