It sure is. First thing I would do is calculate the molarity of the NaOH solution. From there, figuring out the rest is fairly simple, especially since NaOH and H2SO4 are strong bases/acids.
I was assuming that the distillation was of hydrocarbons mixed in water, since you wouldn't perform fractional distillation of mere salt water with nothing else in it.
Alkenes can be cracked as well. An example would be cracking butene to yield propene and ethene.
As for distillation, when you combine two immiscible liquids (such as water and alkanes/alkenes), the total vapor pressure of the mixture is the sum of the vapor pressures of the different liquids...
1. Since we know sulfur is in a -2 oxidation state, that means arsenic is +3. So you could call it either arsenic trisulfide or arsenic (III) trisulfide.
2. Aluminum is always +3, and dichromate is always -2, so the name is aluminum dichromate.
Yes. That way you have an empty 5s subshell and a full 4d subshell, which is energetically favorable compared to a half-full 5s and a partially-full 4d.
I really have no idea where to start with this.
I have a=\frac{2.071\cdot10^{11}A}{mx^{2}} m/s2, where A and m are constants. Since the acceleration is dependent on position, and the position is obviously dependent on acceleration, I don't know how to separate the two in order to do any...