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co-spot of carbonyl & alcohol compounds A 0 Your alcohol product, B (obtained from the NaBH4 reduction reaction of the carbonyl starting material, A) is purified by column chromatography. You obtain the following TLC of the column chromatography fractions. 000 1 TLC Chromatography Fractions 2 0- NaBH4 MeOH H₂O 0 3₂ 0 0 0 1 4 5 B 6 0-1 q OH 7 1.8 cm 2.8 cm 3.2 cm

co-spot of carbonyl & alcohol compounds A 0 Your alcohol product, B (obtained from the NaBH4 reduction reaction of the carbonyl starting material, A) is purified by column chromatography. You obtain the following TLC of the column chromatography fractions. 000 1 TLC Chromatography Fractions 2 0- NaBH4 MeOH H₂O 0 3₂ 0 0 0 1 4 5 B 6 0-1 q OH 7 1.8 cm 2.8 cm 3.2 cm

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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What is the Rf of your alcohol product B? Which fractions would you combine to isolate pure alcohol product B?

 

 

 

co-spot of carbonyl & alcohol compounds A 0 Your alcohol product, B (obtained from the NaBH4 reduction reaction of the carbonyl starting material, A) is purified by column chromatography. You obtain the following TLC of the column chromatography fractions. 000 1 TLC Chromatography Fractions 2 0- NaBH4 MeOH H₂O 0 3 0 0 0 1 4 5 B 6 0-1 1 OH 7 1.8 cm 2.8 cm 3.2 cm
Transcribed Image Text:co-spot of carbonyl & alcohol compounds A 0 Your alcohol product, B (obtained from the NaBH4 reduction reaction of the carbonyl starting material, A) is purified by column chromatography. You obtain the following TLC of the column chromatography fractions. 000 1 TLC Chromatography Fractions 2 0- NaBH4 MeOH H₂O 0 3 0 0 0 1 4 5 B 6 0-1 1 OH 7 1.8 cm 2.8 cm 3.2 cm
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