OH CH3OH HⓇ OCH 3 In the space provided below please show a detailed, stepwise mechanism for the transformation shown above. You must show all intermediates (including proton transfer
OH CH3OH HⓇ OCH 3 In the space provided below please show a detailed, stepwise mechanism for the transformation shown above. You must show all intermediates (including proton transfer
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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Transcribed Image Text:OH
CH3OH
HⓇ
OCH 3
In the space provided below please show a detailed, stepwise mechanism for the
transformation shown above. You must show all intermediates (including proton transfer
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I can see that it's correct to have a hydride shift from a secondary carbocation to another secondary carbocation in this case. I guess what I'm saying is, doesn't hydride shifts only occur when it only produces a more stable carbocation? For instance, secondary carbocation does a hydride shift to a tertiary carbocation. Is it correct to do a hydride shift from a secondary carbocation to another secondary carbocation in this case because the pi bond shifts to produce a tertiary carbocation? And this shift (from a secondary carbocation to another secondary carbocation) only plausible if the pi bond shifts afterwards to create the tertiary carbocation?
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