Please correct answer and don't use hand raiting The substrate below issubstitution reaction.andlose a leaving group to generate a carbocation intermediate during aOTSO primary: willO primary: will notsecondary: willO secondary: will notO tertiary: willO tertiary: will not

Here given substrate isHere the leaving group is OTs (tosylate group). The carbon attached to the…

Answered: The substrate below is substitution…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 28E

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Shown below is a two-step mechanism beginning with nucleophilic attack of water, and subsequent deprotonation with a base. Draw the arrows for the mechanism for both step 1 and step 2 and draw the intermediate product of in the box. + H-O OH + H₂O
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Q.11
The following elimination reaction results in a mixture of products. Explain why the major products obtained in larger quantities than the minor products. Use chemical structures as necessary to justify your answer.
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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. H3C HCI / H2O `NH2 reflux • 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. opy aste Previous Next
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The substrate below is substitution reaction. and lose a leaving group to generate a carbocation intermediate during a OTS O primary: will O primary: will not secondary: will O secondary: will not O tertiary: will O tertiary: will not