1cm^3 = 1L would be the correct answer. One cubic centimeter equals .001 liter, so this equality above is not correct.
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What are you asking???? If the formula had no atoms of oxygen then......
Answer:
HCl
Explanation:
<em>Choices:</em>
<em>CO: 28.01g/mol</em>
<em>NO₂: 46g/mol</em>
<em>CH₄: 16.04g/mol</em>
<em>HCl: 36.4g/mol</em>
<em>CO₂: 44.01g/mol</em>
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It is possible to identify a substance finding its molar mass (That is, the ratio between its mass in grams and its moles). It is possible to find the moles of the gas using general ideal gas law:
PV = nRT
<em>Where P is pressure of gas 0.764atm; V its volume, 0.279L; n moles; R gas constant: 0.082atmL/molK and T its absolute temperature, 295.85K (22.7°C + 273.15).</em>
Replacing:
PV = nRT
PV / RT = n
0.764atm*0.279L / 0.082atmL/molKₓ295.85K = n
<em>8.786x10⁻³ = moles of the gas</em>
<em />
As the mass of the gas is 0.320g; its molar mass is:
0.320g / 8.786x10⁻³moles = 36.4 g/mol
Based in the group of answer choices, the identity of the gas is:
<h3>HCl</h3>
<em />
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.