(Consider the following silica gel TLC plate of compounds A, B, and C developed in hexanes...
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(Consider the following silica gel TLC plate of compounds A, B, and C developed in hexanes 04 ABC -solvent from ongis (ii) (a) Determine the Rf values of compounds A, B, and C. (The distance between the origin and the solvent front is 4 cm. Spot A moved 1.5 cm, Spot B moved 3.5 cm, Spot C moved 3 cm). (ii) (b) Which compound is the most polar? (iii) What would you expect to happen to the Rf values if you used ethyl acetate instead of hexanes as the eluting solvent? (Consider the following silica gel TLC plate of compounds A, B, and C developed in hexanes 04 ABC -solvent from ongis (ii) (a) Determine the Rf values of compounds A, B, and C. (The distance between the origin and the solvent front is 4 cm. Spot A moved 1.5 cm, Spot B moved 3.5 cm, Spot C moved 3 cm). (ii) (b) Which compound is the most polar? (iii) What would you expect to happen to the Rf values if you used ethyl acetate instead of hexanes as the eluting solvent?
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Related Book For
Organic Chemistry
ISBN: 978-1118133576
11th edition
Authors: Graham Solomons, Craig Fryhle, Scott Snyder
Posted Date:
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