Answer:
S = 21.92 %
F = 78.08 %
Explanation:
To find the percent composition of each element in SF6, we must find the molar mass of SF6 first.
Molar mass of SF6 = 32 + 19(6)
= 32 + 114
= 146g/mol
mass of Sulphur (S) in SF6 = 32g
mass of Fluorine (F) in SF6 = 114g
Percent composition = mass of element/molar mass of compound × 100
- % composition of S = 32/146 × 100 = 21.92%.
- % composition of F = 114/146 × 100 = 78.08%.
Answer:
Melting: the substance changes back from the solid to the liquid. Condensation: the substance changes from a gas to a liquid. Vaporization: the substance changes from a liquid to a gas. Sublimation: the substance changes directly from a solid to a gas without going through the liquid phase.
Explanation:
Answer:
5.004kg
Explanation:
Combustion of carbon
C+O2=CO2
from the relationship of molar ratio
mass of carbon/molar mass of carbon=volume of CO2 produced\molar vol(22.4 dm3)
mass of carbon =1000kg
atomic mass of carbon =12
volume of CO2 produced=1000×22.4/12
volume of CO2 produced =1866.6dm3
from the combustion reaction equation provided
CO2 (g) + 2NH3 (g) ⟶ CO (NH2 )2 (s) + H2 O(l)
applying the same relationship of molar ratio
no of mole of CO2=no of mole of urea
therefore
vol of CO2\22.4=mass of urea/molar mass of urea
molar mass of urea=60.06g/mol
from the first calculation
vol of CO2=1866.6dm3
mass of urea=1866.6×60.06/22.4
mass of urea=5004.82kg
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