Did the overall reaction shown here occur by an Sn2, SN1, E2, or E1 mechanism? How do you know? Draw the complete, detailed mechanism to account for the formation of both products. ОН + H,O
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- Consider the intramolecular nucleophilic substitution reaction shown here. Does the stereochemistry of the product suggest an Sn1 or SŅ2 mechanism? Draw the complete mechanism for this reaction, including curved Br OH NaOH CH3 H3C CH3 Br H3C H arrows.Draw a plausible mechanism for the reaction shown below. Et Ме OH ..Me 1) Excess EtMgBr 2) Hо Et "CIThe reaction shown here proceeds via a carbocation rearrangement. Draw a complete, detailed mechanism to account for the product. Explain why the carbocation rearrangement is favorable. CH;OH Br
- Draw the complete, detailed mechanism for the reaction shown here and predict the major products, including stereochemistry. Br SH HS ? DMSO BrPredict the major thermodynamic and major kinetic product from the following reaction. Label the major products accordingly. Draw the mechanism (arrow pushing) for each product (2 mechanisms total). Please explain stepsDraw a detailed mechanism for the following addition of HBr across a double bond and explain why the given product is the major product
- Can you please show me full detailed mechanism of this reaction? Please include formal charges, intermediates, and electron arrows.Complete all the reactions/show the products, and for each reaction clearly and thoroughly explain which mechanism (E1, E2, SN1, SN2) is predominant and how it effects the product formation.10. Draw the complete, detailed mechanism (curved arrows) for the following reaction, and predict the major product. CH3 ▪OH 1. DMSO (COCI)2 2. Et3N H
- The reaction shown here is called the pinacol rearrangement. A carbocation rearrangement is believed to be involved. Propose a reasonable mechanism for this reaction. HO онDraw a mechanism to account for the formation of the NaOH product in the reaction shown here. Hint: Under these A conditions, deprotonation of a propargylic (C=C-CH) carbon is reversible.Q5. Draw the all products and a detailed mechanism for the following reaction? -OCH2CH3 Br CH3CH2OH