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- Consider the nucleophilic substitution reaction shown here. Based on the stereochemistry, does it proceed by an Sy1 or Sy2 mechanism? Explain. OH KOCH3 Enantiomer CH;OH `OCH3Show Transcribed Text H₂, Pd/C, EtOH MeMgBr (excès) puis H3O+ Me₂CuLi, Et₂O puis H₂O+ Please draw the mechanism step by step ? ? ?Considering stereochemistry, draw the resulting E2 elimination product when H, is removed. H₂ H All H Br |||| X AJ U: S G
- Given that an E2 reaction proceeds with anti periplanar stereochemistry, draw the products of each elimination. The alkyl halides in (a) and (b) are diastereomers of each other. How are the products of these two reactions related?Predict the substitution products of the following reaction and pay attention to stereochemistry. Draw the mechanism for this SN2 substitution reaction. Draw all pertinent molecular orbitals (i.e., bonding, anti-bonding, non-bonding) involved in this mechanism. Br OMe NaSPhQ10. Propose a plausible mechanism for the given transformation. Ignore stereochemistry. NaOMe I CHO
- Determine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OHClassify the following reaction as an Sn1, Sn2, E1, E1cB, E2 reaction. Can you show me the leaving group and explain how to find a leaving group? And how to identify the other reactions?3. Draw the expected product/products of the following elimination reaction schemes and state if they are undergoing E1/E2. ✩ Note TsCl, Et3N converts the -OH to -OTS with the same stereochemistry. a) b) Me Me OH OH Et Et H3O+ 1) TSCI, Et3N 2) NaH, DMF ? ?
- Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the product of this elementary step in an E1 mechanism. Include all lone pairs. Ignore stereochemistry. Ignore byproducts. :0 H dant H₂O H heat H Qtempt.php?attempt3D1101388&cmid%3D371560 Draw a detailed mechanism showing the formation of all products, be sure to draw all intermediate and show the movement of electros by arrows. F. -Br -OCH3 -OCH3 Heat A - BI aQ5. Draw the product and propose the mechanism of the following reaction. Me H OH pyridine + SOCI₂