Now suppose, instead, that 5.678 g of a volatile solute is dissolved in 150.0 g of water. This solute also does not react with water nor dissociate in solution. The pure solute displays, at 20°C, a vapour pressure of 1.754 torr. Again, assume an ideal solution. If, at 20°C the vapour pressure of this solution is also 17.344 torr. Calculate the molar mass of this volatile solute.

59.9 g/mol is the molar mass for the solute

Explanation:

Lowering vapor pressure → ΔP = P° . Xm

P° → Vapor pressure of pure solvent

ΔP = P° - Vapor pressure of solution

Xm = Mole fraction of solute

17.54 Torr  - 17.344 Torr = 17.54 Torr . Xm

0.196 Torr / 17.54 Torr = Xm → 0.0112

These are the moles of solute / Total moles

Total moles = Moles of solute + Moles of solvent

We determine the moles of solvent → 150 g . 1mol/ 18 g = 8.33 moles

Now we can make this equation:

0.0112 = Moles of solute / Moles of solute + 8.33 mol

0.0112 Moles of solute + 0.0933 = Moles of solute

0.0933 = Moles of solute - 0.0112 Moles of solute

0.0933 = 0.9888 moles of solute → 0.0933 / 0.9888 = 0.0947 moles

Finally we can determine the molar mass (mol/g)

5.678 g / 0.0947 mol = 59.9 g/mol

explanation:

the largest database of organic compounds lists about 10 million substances, which include compounds originating from living organisms and those synthesized by chemists. the number of potential organic compounds has been estimated at 1060—an astronomically high number. the existence of so many organic molecules is a consequence of the ability of carbon atoms to form up to four strong bonds to other carbon atoms, resulting in chains and rings of many different sizes, shapes, and complexities. the simplest organic compounds contain only the elements carbon and hydrogen, and are called hydrocarbons. even though they are composed of only two types of atoms, there is a wide variety of hydrocarbons because they may consist of varying lengths of chains, branched chains, and rings of carbon atoms, or combinations of these structures. in addition, hydrocarbons may differ in the types of carbon-carbon bonds present in their molecules. many hydrocarbons are found in plants, animals, and their fossils; other hydrocarbons have been prepared in the laboratory. we use hydrocarbons every day, mainly as fuels, such as natural gas, acetylene, propane, butane, and the principal components of gasoline, diesel fuel, and heating oil. the familiar plastics polyethylene, polypropylene, and polystyrene are also hydrocarbons. we can distinguish several types of hydrocarbons by differences in the bonding between carbon atoms. this leads to differences in geometries and in the hybridization of the carbon orbitals.

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