I have a homework question for which the correct answer is given. However, I don't understand why there isn't a 1,2-hydride shift during the carbocation phase of the reaction to make the carbocation more stable. Draw the products formed when the following alkyne is treated with each set of reagents. Be sure toanswer all parts.[1] H₂O, H₂SO4, HgSO4SH-HSO4edit structure ...why doesn't this happen?HHHSOчOHH

Step 1:First alkyne act as a nucleophile and attack the mercuric sulphate to form mercurinium ion So…

Draw the products formed when the following alkyne is treated with each set of reagents. Be sure to answer all parts. [1] H₂O, H₂SO4, HgSO4 SH-HSO4 edit structure ... why doesn't this happen? H H HSOч OH H

Draw the products formed when the following alkyne is treated with each set of reagents. Be sure to answer all parts. [1] H₂O, H₂SO4, HgSO4 SH-HSO4 edit structure ... why doesn't this happen? H H HSOч OH H

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.2: Other Aromatic Substitutions

Problem 4P: When benzene is treated with D2SÅª4. deuterium slowly replaces all six hydro gens in the aromatic...

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I have a homework question for which the correct answer is given. However, I don't understand why there isn't a 1,2-hydride shift during the carbocation phase of the reaction to make the carbocation more stable.

Draw the products formed when the following alkyne is treated with each set of reagents. Be sure to
answer all parts.
[1] H₂O, H₂SO4, HgSO4
SH-HSO4
edit structure ...
why doesn't this happen?
H
H
HSOч
OH
H

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