Tlc fluorene 9 fluorenol 9 fluorenone

A mixture of Fluorene 1 and Fluorenone 2 was separated by column chromatography. Fluorene 1 Fluorenone 2 Mp ? Column chromatography was invented by Tswett in so that his study of the chemistry of chlorophyll could be facilitated. Tswett made significant advances in the method and demonstrated its applicability to the separation of many different kinds of mixtures.

Tlc fluorene 9 fluorenol 9 fluorenone

How to Write a Summary of an Article? In table format, provide the Rf values you recorded for each of the 3 compounds in Part I.

List compound on one axis of your table and solvent system on the other.

Tlc fluorene 9 fluorenol 9 fluorenone

Also rank the 3 compounds in order of decreasing polarity this compound ranking can be based on structure as well as on these TLC results.

Explain each of your rankings.


Fluorene has the least amount of polarity based on structure and when it was mixed with non-polar and slightly polar solvents, its mobile phase moved the furthest. Based on the compounds and the Rf values, the compounds with larger Rf values means that the mobile phase traveled the furthest on the polar silica gel plate.

Also, the compounds with the larger Rf value indicates that it was a less polar structure, as it interacts less strongly with the polar absorbent on the TLC plate.

Based on structure, which of the 3 compounds can hydrogen bond to the silica gel? The 9—fluorenol is the only one out of the three compounds that can hydrogen bond to the silica gel plate. Based on Rf values shown in question one, it had a lower Rf value, generally meaning compounds that can hydrogen bond to the silica gel will have the lower Rf values.

If you attempted to separate a mixture of the 3 compounds using liquid chromatography see Ch. Briefly explain your answer.

Tlc fluorene 9 fluorenol 9 fluorenone

Based on TLC, is your dibromide pure and different from trans-stilbene? In your answer give Rf values for each compound make sure to give solvent system as well! Do your TLC results prove that your product is really trans-stilbene dibromide? Based on my results, my dibromide compound is different than trans-stilbene.

The trans-stilbene and the dibromide do not share identical Rf values, but we can assume since there is only a 0. Do the tablets seem to contain caffeine?

The mechanism to convert 9-fluorenol to 9-methoxy fluorene, Ask an Expert

Does TLC prove your answer? Since there was a difference of 0. Also, since the difference was so minimal between the two compounds it can be suggested that there were significant amounts of caffeine in the unknown tablet.

The mobile phase is an inert gas, generally He2 or N2 does not compete with the stationary phase like TLC or LC, where the mobile phase actively competes with the stationary phase. The mobile phase does not interact with the compounds during GC, while they do interact in liquid chromatography and TLC.

Later, we will cover mass spectrometry, and will likely also mention a combined analytical technique called GC-MS gas chromatography-mass spectrometry. GC-MS combines gas-liquid chromatography and mass spectrometry to identify different substances within a test sample.

Written by Kevin. Abstract: This experiment will observe the reduction of fluorenone to fluorenol (Fluorenone Reduction) through thin-layer chromatography. This reduction will be monitored at different time intervals and under different solvent concentrations to be compared with two reference solutions of fluorenone and fluorenol. Fluorenol Buy Fluorenol Fluorenol User Reviews Contact Fluorenol Buy Fluorenol Fluorenol User Reviews Contact Fluorenol Safety. Direct Fuorenol Source. Fluorenol Safety Date Sheet. Powered by Create your own unique website with customizable templates. Get Started. Since the alumina, diethyl ether, and the fluorenone are all polar, the fluorenone will travel faster through the alumina than would the fluorene, because there is no attraction between all these polar compounds which will allow it to move faster, rather than a nonpolar and polar chemical having an attration towards each other and thus moving.

It is used to perform specific tests that can positively identify the actual presence of a particular substance in a given sample. If the Rf values are identical, one can assume that the substance are the same and the GC-MS would be better to differentiate the Rf values for two separate substances in a given sample, giving a more accurate identification.Prior art keywords fluorene process according fluorenone reaction process Prior art date Legal status (The legal status is an assumption and is not a legal conclusion.

= Fluorenone, = Fluorene. Flask three was only supposed to have Fluorenone but this shows contamination of the other compound. For a mixture of fluorene, fluorenone and -fluorenol is examined by TLC and gives the following Rf values: , , | Identify .

Sign Up for Email Customer Service +1 [email protected] Get help on 【 Chromatographic Seperation of Fluorene and Fluorenone Essay 】 on Graduateway Huge assortment of FREE essays & assignments The best writers! It cannot affect the same degree of separation as TLC, but its advantage over TLC is the fact that large amounts of mixtures (over 5 g) can easily be treated by this method.

Electronic absorption, excitation and fluorescence spectra of fluorenone and 4-hydroxyfluorenone were recorded at room temperature in several aprotic solvent of varying polarities.

It is well known that fluorenone possesses a closely lying excited state of different character,. For the absorption spectra of 9Fl and 4HOFl, Eqs. Reduction of fluorenone to fluorenol by sodium borohydride Oxidation of Fluorene to Fluorenone Mechanism; Reduction of Fluorenone to Fluorenol Next Lesson.

Huisgen Cycloaddition: Mechanism.

Column Chromatography and TLC Lab Analysis