Your Question About Easy Weight Loss

Michael asks…

Help with determining concentration of diethyl ether?

2.5 L of diethyl ether was spilt on the floor of a lab with the volume of 486m3. The STEL (short term exposure limit), which is the maximum permissable concentration in air allowed of a substance in a workplace is 1520 mg/m3. The density of diethyl ether is 255. Assuming all of the ether will evaporate rapidly into the air. Will the concentration of diethyl ether in the air exceed the STEL?

weight loss cardiff answers:

The density of diethyl ether at 20 deg C is 0.7135 g/mL. (Your value of 255 – unknown units – is wrong).
2.5 L x 1000 mL/L x 0.7135 g/mL x 1000 mg/g = 1,784,000 mg
1,784,000 mg / 486 m^3 = 3670 mg/m^3
3670 mg/m^3 exceeds 1520 mg/m^3

John asks…

what is the force between hexane and diethyl ether?

Is it dipole-induced dipole because diethyl ether is polar? Hexane isn’t polar right?

weight loss cardiff answers:

There are only london dispersion forces between the two chemicals, because hexane is nonpolar, and cannot have any other intermolecular attractions

Richard asks…

How do you extract Diethyl ether from starter fluid?

I heard that it can simply be done with water but petroleum distillates do not dissolve in water and the distillates stay mixed with the ether but I dont know.

weight loss cardiff answers:

In short, not really. The only way to effectively separate petroleum distillates from diethyl ether in starter fluid is by fractional distillation. This requires appropriate equipment and training in relevant lab procedures, can be EXTREMELY dangerous, and is outside of the skillset of most people.

Some websites and experience reports mention a “water extraction” procedure that involves shaking a mixture of distilled water and starter fluid.

The so-called “water extraction” method is simplistic and ineffective, since petroleum distillates and water are not miscible (petroleum distillates do not dissolve in water), and the distillates stay mixed with the ether, because of their common chemical nature. In fact, if the components in the water-insoluble fraction were to separate, which is highly unlikely, the density of ether would put it at the bottom, closest to the water, at the water:non-polar interface, making it very difficult to isolate. Because ether is slightly soluble in distilled water, the volume of the ether in the water-insoluble fraction may actually be reduced by repeated shaking and separating.

Ether is slightly soluble in distilled water and heptane is insoluble. Hence, if one were to try to clean up starting fluid via repeatedly shaking with distilled H2O and then separating the layers, you not only don’t end up with very good ET2O, but you are actually reducing the amount of ether that you have.

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