7.13 A proton (H*) from trifluoromethanesulfonic acid, CF3SO2OH, can add to the alkyne shown here to yield two different carbocation products. (a) Draw the mechanism for each of these steps, along with the corresponding products. (b) Which carbocation is more stable? H3C H₂ C-C=CH + H-OSO₂CF3 H₂ ?

7.13 A proton (H*) from trifluoromethanesulfonic acid, CF3SO2OH, can add to the alkyne shown here to yield two different carbocation products. (a) Draw the mechanism for each of these steps, along with the corresponding products. (b) Which carbocation is more stable? H3C H₂ C-C=CH + H-OSO₂CF3 H₂ ?

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 31E

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