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Interpretation:
A suitable solvent to analyze the mixture of alcohol and
Concept introduction:
Thin-layer chromatography is an analytical technique used to identify whether two compounds are identical or not and also to find the number of compounds in a mixture.
Metal, glass or plates made of plastics are utilized in TLC that are coated by a thin layer of adsorbent and it acts as a stationary phase. The stationary phase usually used is polar silica gel. A mixture of solvents or single pure solvent is the mobile. It is also known as a developing agent. Mostly nonvolatile solid organic samples are analyzed by thin-layer chromatography.However, TLC cannot be used for volatile liquid compounds because it leads to loss of the sample by evaporation from the TLC plate.
In TLC analysis, mixture in a low quantity is taken for separation and dissolved in the suitable solvent and applied on the TLC plate. Then TLC plate is kept in the closed chamber immersed in mobile phase known as developing solvent. Through capillary action the solvent rises on the stationary phase. As the solvent rises on the plate, the sample is distributed between the mobile phase and the stationary phase on the basis of their retention values. The more the compound interacts with the stationary phase, the more slowly it moves on the TLC plate. When silica gel that is polar in nature behaves as the stationary phase then mobile solvent rises with the nonpolar substances up on the plate most rapidly. In the chromatogram the polar substances rise up plate with lowest rate.
The ratio of distances covered by the compound to the distance covered by developing solvent or mobile front is known as retention factor
The
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Chapter 18 Solutions
Laboratory Techniques in Organic Chemistry
- Basic strength of organic bases.arrow_forwardNucleophilic Aromatic Substitution: What is the product of the reaction? What is the name of the intermediate complex? *See imagearrow_forwardPredict the final product. If 2 products are made, list which should be “major” and “minor” *see attachedarrow_forward
- 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
- EBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT
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