Ether and hexane are considered to non-polar solvents, in all honesty, ether is only slightly, slightly, slightly more polar than hexane. If a TLC experiment was completed with 9:1, hexane:ether, would you expect the 2- methylcyclohexanol to have a MUCH MUCH MUCH lower Rf, or, a MUCH MUCH MUCH higher Rf value than the alkene isomer products? (a) i just don't know (b) higher (c) lower

Ether and hexane are considered to non-polar solvents, in all honesty, ether is only slightly, slightly, slightly more polar than hexane. If a TLC experiment was completed with 9:1, hexane:ether, would you expect the 2- methylcyclohexanol to have a MUCH MUCH MUCH lower Rf, or, a MUCH MUCH MUCH higher Rf value than the alkene isomer products? (a) i just don't know (b) higher (c) lower

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy

Section12.SE: Something Extra

Problem 16AP: Camphor, a saturated monoketone from the Asian camphor tree, is used among other things as a moth...

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Cyclohex-2-enone has two protons on its carbon–carbon double bond (labeled Ha and Hb) and two protons on the carbon adjacent to the double bond (labeled Hc). (a) If Jab = 11 Hz and Jbc = 4 Hz, sketch the splitting pattern observed for each proton on the sp2 hybridized carbons. (b) Despite the fact that Ha is located adjacent to an electron-withdrawing C = O, its absorption occurs upfield from the signal due to Hb (6.0 vs. 7.0 ppm). Offer an explanation.
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