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 CHEMIS
- PQ-10. What is the major product of this reaction? (A) (C) 930 Me HO O=S=O O-8-CF, C 어 Me H+ OH 270 O 0-5-0 O=S=O O-S-CF CF3 2arrow_forwardPredict the major organic product(s) of the following reactions. Include stereochemistry when necessary. Write NR if no reaction, try to explain.arrow_forwardQ2: Explain why epoxides that react in an SN1 manner will not show any stereochemical inversion in the product. Q3: Rationalize why Alcohol B will react under the indicated reaction conditions, but Alcohol A will not. A ☑ OH B OH PBr3 R-Brarrow_forward
- Q1: Predict the major organic product(s) of the following reactions. Include stereochemistry when necessary. Write NR if no reaction, try to explain. 1.) LDA, THF 2.) СОН CI OH H2SO4, heat OH m...... OH 1.) PCC, CH2Cl2 2.) CH3CH2MgBr, THF 3.) H3O+ 4.) TsCl, pyr 5.) tBuOK, tBuOH 1.) SOCI 2, CHCI 3 2.) CH3CH2ONA, DMF OH 1.) HBr 2.) Mg, THF 3.) H₂CO, THE 4.) H3O+ OH NaH, THFarrow_forwardWhat is the stepwise mechanism for this reaction?arrow_forwardDraw the major product of this reactionarrow_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


