Hexane has stronger IMF's than cyclohexane since it has more hydrogen atoms to hydrogen bond with. Hexane has stronger IMF's than cyclohexane due to its higher molar mass. Cyclohexane has stronger IMF's than hexane due to its shape. The IMF's are the same strength since they both have weak dispersion forces.

Hexane has stronger IMF's than cyclohexane since it has more hydrogen atoms to hydrogen bond with. Hexane has stronger IMF's than cyclohexane due to its higher molar mass. Cyclohexane has stronger IMF's than hexane due to its shape. The IMF's are the same strength since they both have weak dispersion forces.

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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Alkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.