Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the followingreactionонH2SO4 (trace)+CH3OHrefluxYou do not have to consider stereochemistry.Include all valence lone pairs in your answer.. Do not include counter-ions, eg, Na+, 1, in your answer.In cases where there is more than one answer, just draw one.

Question
Asked Mar 2, 2019

Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction.

  • You do not have to consider stereochemistry.
  • Include all valence lone pairs in your answer.
  • Do not include counter-ions, e.g., Na+, I-, in your answer.
  • In cases where there is more than one answer, just draw one. 
Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following
reaction
он
H2SO4 (trace)
+CH3OH
reflux
You do not have to consider stereochemistry.
Include all valence lone pairs in your answer.
. Do not include counter-ions, eg, Na+, 1, in your answer.
In cases where there is more than one answer, just draw one.
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Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction он H2SO4 (trace) +CH3OH reflux You do not have to consider stereochemistry. Include all valence lone pairs in your answer. . Do not include counter-ions, eg, Na+, 1, in your answer. In cases where there is more than one answer, just draw one.

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In carbonyl compounds, The Carbon of -C=O attains a partial positive charge due to electronegativ...

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