Question

Why are some molecules more soluble in the aqueous layer and some in the organic layer?...

Why are some molecules more soluble in the aqueous layer and some in the organic layer?
How do you decide which compounds are more soluble in water?

Homework Answers

Answer #1

we have a principal for solubility

Like dissolve like.   

it means polar compound dissolve in polar solvents only , non-polar compounds dissolve in non polar solvents only.

suppose take NaCl   which is polar   it dissolve in polar solvent   only like water.

take kirosine will not mix with water can mix with benzene , because both are non-polar.

more the polarity of compound more will be the solubility in water.

one more fact is that if compound is able to form hydrogen bonding it also can dissolve in water.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
You perform an extraction to remove a compound dissolved in an aqueous layer into an organic...
You perform an extraction to remove a compound dissolved in an aqueous layer into an organic layer. 80% of the compound is removed after one extraction. You perform the extraction two more times with equivalent amounts of the organic layer. You should expect to extract approximately how much of the compound from the water? 99.2% What is the equation to do this?
Suppose you have discovered a new organic molecule and it is somewhat soluble in water even...
Suppose you have discovered a new organic molecule and it is somewhat soluble in water even though it is more soluble in dichloromethane or ether solvents. If you do a single extraction, you get only 60% of your material to transfer from the water to the organic layer. How many washes would it take to extract over 90% of your organic material from the water layer. Explain.
How do you dry the organic dichloromethane layer? (To dry an organic solvent means to get...
How do you dry the organic dichloromethane layer? (To dry an organic solvent means to get rid of any water molecules that might be in the organic layer.) How do you prevent uneven boiling or even bumping while heating the organic layer to remove dichloromethane? Why do you have to work under the hood while removing dichloromethane on a hot plate? (2 points)
Compare and Contrast two organic macromolecules. Which organic molecules are always, sometimes, never water soluble?
Compare and Contrast two organic macromolecules. Which organic molecules are always, sometimes, never water soluble?
Draw mechanisms for reaction of catechin and Na2CO3 (Aqueous Layer) Caffeine and dichloromethane (Organic layer) Na2SO4...
Draw mechanisms for reaction of catechin and Na2CO3 (Aqueous Layer) Caffeine and dichloromethane (Organic layer) Na2SO4 (drying agent) + Organic layer (process of eliminating any residual water).
An extraction system consisting of hexanes as the organic layer and water ias the aqueous layer...
An extraction system consisting of hexanes as the organic layer and water ias the aqueous layer s excellent for separating a carboxylic acid from benzaldehyde.
Why are organic carboxylates far more soluble in water than carboxylic acids ?
Why are organic carboxylates far more soluble in water than carboxylic acids ?
Your experiment consists of three stages: Separation, Recovery, and Purification. In the Separation stage, you are...
Your experiment consists of three stages: Separation, Recovery, and Purification. In the Separation stage, you are physically separating three compounds, a carboxylic acid, a phenol, and a neutral compound. In the procedure, which compound is separated first? Question 6 options: neutral carboxylic acid phenol 1. The purpose of RECOVERY is to change the chemical form of the extracted components back to its original molecular form. What reagent is added to recover the carboxylic acid and phenol from the aqueous layer?...
A dilute aqueous solution of an organic compound soluble in water is formed by dissolving 2.53...
A dilute aqueous solution of an organic compound soluble in water is formed by dissolving 2.53 g of the compound in water to form 0.250 L of solution. The resulting solution has an osmotic pressure of 0.673 atm at 25°C. Assuming that the organic compound is a nonelectrolyte, what is its molar mass?
Suppose you isolated the two compounds above but failed to label which came from the aqueous...
Suppose you isolated the two compounds above but failed to label which came from the aqueous layer and which came from the organic layer. How could IR help you decide which was which? (E.g., the benzyl would show a peak around _____ representing _____, but the 3- nitroaniline would not.) Provide 3 differences expected