
Interpretation:
The reason for the level of elution solvent to not drop below the top of the adsorbent should be determined.
Concept introduction:
Liquid chromatography is used for purification of high boiling compounds. It is known as column chromatography. In liquid chromatography, column is packed by stationary phase. Usually, a solid adsorbent with a liquid coated on it is used as stationary phase. Often a pure liquid or solution of liquids composes the mobile phase. It is also called the elution solvent.
The elution solvent comes down the column under the influence of gravity. Selective interactions are responsible for separation of the sample among stationary and mobile phases. The sequence of elution of compounds from sample depends on the polarity of mobile and stationary phases.

Explanation of Solution
The packing of a column is an important factor for the success of the chromatographic separation in addition to the choice of adsorbent and elution solvents.
If cracks or channels are present in the column or if the top surface is not flat, then separation in the chromatographic column will be poor.
If the adsorbent becomes dry, it may drift away from the walls of the column and form channels. Once a chromatographic separation begins, it is essential to finish it without interruption.
Want to see more full solutions like this?
Chapter 19 Solutions
Laboratory Techniques in Organic Chemistry
- Nucleophilic Aromatic Substitution: What is the product of the reaction? *see imagearrow_forwardShow the correct sequence to connect the reagent to product. * see imagearrow_forwardThe answer here says that F and K have a singlet and a doublet. The singlet and doublet are referring to the H's 1 carbon away from the carbon attached to the OH. Why don't the H's two carbons away, the ones on the cyclohexane ring, cause more peaks on the signal?arrow_forward
- Draw the Birch Reduction for this aromatic compound and include electron withdrawing groups and electron donating groups. *See attachedarrow_forwardShow the correct sequence to connect the reagent to product. * see imagearrow_forwardBlocking Group are use to put 2 large sterically repulsive group ortho. Show the correct sequence toconnect the reagent to product with the highest yield possible. * see imagearrow_forward
- Elimination-Addition: What molecule was determined to be an intermediate based on a “trapping experiment”? *please solve and see imagearrow_forwardShow the correct sequence to connect the reagent to product. * see imagearrow_forwardPredict the final product. If 2 products are made, list which should be “major” and “minor”. **see attachedarrow_forward
- Principles of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage LearningEBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT
- Macroscale and Microscale Organic ExperimentsChemistryISBN:9781305577190Author:Kenneth L. Williamson, Katherine M. MastersPublisher:Brooks Cole


