If you were to monitor the reaction mechanism for the hydroboration by TLC (Thin Layer Chromatography), would you expect the starting material (1-octene) or the product (1-octanol) to have a lower Rf? Please explain your answer, being sure to mention important intermolecular forces. Why does the hydroboration part of the reaction have to be performed in anhydrous conditions?

If you were to monitor the reaction mechanism for the hydroboration by TLC (Thin Layer Chromatography), would you expect the starting material (1-octene) or the product (1-octanol) to have a lower Rf? Please explain your answer, being sure to mention important intermolecular forces. Why does the hydroboration part of the reaction have to be performed in anhydrous conditions?

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter20: Nucleophilic Substitution Reactions: Competing Nucleophiles

Section: Chapter Questions

Problem 9Q

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