Question

Predict the behavior of your unknown if it were subjected to TLC in propanol (draw a...

Predict the behavior of your unknown if it were subjected to TLC in propanol (draw a sketch of the TLC plate). Could propanol be used to separate the two compounds in your unknown by column chromatography? Explain.

Answer the same questions but using hexanes as the solvent.

Unknown contains Ferrocene and Acetylferrocene.

Homework Answers

Answer #1

Propanol is more polar solvent.

If we run the TLC in polar solvent such as propanol, then all the unknown compounds will run together to the maximum Rf value and there is no proper seperation can be observed.

So, Propanol alone is not a good solvent for TLC sepreration. The both unknown compounds will show same Rf.

If we run the column with the same solvent system, then both unknown compounds will elute together

In the same way. If we run the TLC in Hexane (Hexane is non-polar solvent). The unknown compounds wer wont move in TLCand they cannt be seperated in Hexane.

TLC profile in Hexane

If we use Hexane for elution in column chromotography, the both unknowns cann't run in column.

So Hexane is not a good solvent for separation.

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
Ethyl acetate is another common organic solvent used in the type of TLC experiment you performed:...
Ethyl acetate is another common organic solvent used in the type of TLC experiment you performed: it has a higher molecular weight and boiling point than either petroleum ether or diethyl ether, and is more polar than them as well. If ethyl acetate had been used as the mobile phase for a TLC analysis of F and AF, how would their Rf values compare to those found using the 1:1 solvent mixture you used? That is, predict how the behavior...
You run a reaction with column chromatography and you find that you have multiple products (cyclohexene...
You run a reaction with column chromatography and you find that you have multiple products (cyclohexene from cyclohexanol). You predictyou have the alcohol functionality you were trying to make and the alkene from the eliminated product (some of the alochol must have elimited to form the alkene). You run a few TLCs to find a good solvent to run a column in order to separate two products. You decide on a 10% ethyl acetate in hexanes because it allows one...
Pre -Laboratory Assignment 1. Briefly describe or define each of the following terms as they pertain...
Pre -Laboratory Assignment 1. Briefly describe or define each of the following terms as they pertain to this experiment. a) Spotting a plate b) Developing a plate c) Visualizing d) Rf e) eluent f) stationary phase 2. List the following solvents in order of increasing polarity: dichloromethane, acetone, toluene and cyclohexane. 3. Your unknown sample moved a distance of 25 millimeter from its origin while the distance traveled by the eluent from the origin was 55 millimeters. What is the...