1) 2) Please give a detailed stepwise mechanism for the following reactions. All arrows, charges, and intermediates must be shown. NaOH, H2O, heat i CHÍNH, + N CH3OH H
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- Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. 1) CH3CH2M9B CH3OH H+ (ехcess) но 2) H30*, H2O B A OCH3Please give a detailed stepwise mechanism for the following reactions. All arrows, charges, and intermediates must be shown. 1) CN H*, H₂O, heat Яон OHProvide reaction mechanisms for the following transformations
- Give the major organic product of the following reaction. 1) ВН3/THF 2) NaOH, H2O2 HO OH HO- OH There is no reaction under these conditions or the correct product is not listed here.Write the appropriate reagents, conditions and products for the following transformations, in a single step. OH II HNO, ? (1) H,SO,i) ii) 1. Propose a mechanism for the following reactions. H (CH3)2NH H* NaOH EtOH
- 2) reaction sequences to carry out those transformations. Draw the expected product of each step proposed. Substantial partial credit can be obtained for incomplete or incorrect answers. You may present your solutions on the following blank page if you need the the following reaction transformations, and propose room. H3C CH, H3C CH3 of HN- -NH HO,C Co,H но H,C CH3 CEN OCH3 OCH3Provide the mechanism for the following reaction (1) PhMgBr (2 equiv) (2) H3O+ workup OH5) Provide the expected mechanism for the following reaction. Please show all intermediates and use arrows to show the movement of electrons (you do not have to show transition states). (1 pt) ii CI NaOH (2 equiv)
- Provide detailed step-wise mechanism for the following reaction. Be sure to show all intermediates, formal charges, and show the movement of electrons with curved arrows. a 4+H₂Q 044 OHPropose a mechanism for the following reaction. Draw out the each step of the reaction including ALL intermediates. CI A CO₂ Et + inte NaO6t EtOH CTS Eta₂c,a) Using your knowledge of organic reaction mechanisms, explain the formation of EACH product (A,B) in the following reaction. This will require you to write out MULTIPLE mechanisms (i.e. each product comes from a different reaction pathway). Hint: all reaction pathways start from the same intermediate: NaH is a strong base but cannot deprotonate an sp3 C-H bond! OH он 1) NaH (0.5 equiv) Br + 2) H20 A B b) Briefly explain why there is no epoxide (formed via an intramolecular substitution reaction) in the product mixture of the above reaction?