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- What will be the major product of the following reaction and what is the likely mechanism for its formation? (CH;);COK Br racemic OCCCH3)3 OCCH3)3 ÓCCCH3)3 A B C D EWhich of the following molecules will NOT lead to a successful synthesis of a Grignard reagent upon reaction with magnesium? CI https://ibb.co/54Jw34p 2 Me. OMe https://ibb.co/6655LTH Br но https://ibb.co/2nfzPmX O Me `Br https://ibb.co/wo93ymS 2 Br MeO https://ibb.co/Hq2s6ck 2The SN2 reaction ur 1-chloro-3-methylbutane with hydroxide OH is relatively slow, but it can » be accelerated by the addition of a small amount of Nal. How can this catalysis be explained? (In other words. how is iodide acting as a catalyst?) CONCISELY explain. nd favor and
- Short Anver Question 11. Povide ONLY the MAJOR NO MECHANISMS for the following reactions-you include the regiochemistry and stochemistry when necessary HEY ROOR ✓ 1)0, 2) DMS 1) H₂0Ac), HO 2) Na 1) R₂BH 2) NaOH, H₂O₂What is(are) the major final product(s) formed during the following sequence of reactions? 01 11 V 1.0₂ 2. (CH₂)₂S C₂H₂O 2 identical molecules ||| =PPhy < IV орна35) What is the correct order of reagents to achieve the following synthesis? A) i) NH2NH2, H3O* (aq); ii) NaOH (aq) & A Reactant structure: Target molecule: B) i) LIAIH«, THF; ii) H2O & A C) i) NABH4, EtOH; ii) H2O & A CH3 CH3 D) i) DIBAL-H ii) H3O* (aq) & A
- 5. Provide a base to prepare the following major products for each of the following E2 reactions. Explain. Chemistr S Br b) @ OT “Chérsistry SE Chemistry Skipsowing reactions proceeds via an SN1 or SN2 of the reaction: (b) S2 pro85 39 Br tort atubong auonsV HMPAnoitutitadua14C labelled OTS RCO H 16. →product; Product of this reaction is : no label ОCOR OCOR (a) (b) (c) both (a) and (b) (d) None of these
- (b) + Suggest a plausible-mechanism-for the synthesis of the compound-shown-below H30Keller (c) HOW ОН provide the mechanism: Bonus ICA H₂SO4 НО III.. ...OH(d) With reference to the following reaction scheme: Me tBu 13 Reagent(s)? Me!!!. OH E noitesu cheq lo 19van A tBu 146 jqmolts nA (6) lobis boaaono gniau bauogmos prins bns to ouxims ni besteni batles M bon Jelsistum woler (1) Draw cyclohexanone 13 in the lowest energy chair conformation. (ii) Suggest an appropriate reagent to achieve this stereoselective reduction of cyclohexanone 13 to cyclohexanol 14 and explain your choice of reagent (curved arrow mechanisms are not required).