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Solved in 3 steps with 1 images
- Please explain the synthesis. Identify SN1, SN2, E1, E2, nucleophiles and ekectrophiles.#16f. Provide the missing reactants, reagents, or products for the following reaction sequences below.Compound A reacts with the reagents shown in the image. Write the mechanism, step by step, for the formation of product B. Note that B has the molecular formula C14 H18 O.
- 4. Provide a mechanism for Boc-deprotection IN N. TFA H₂N OH Дон OH R RDraw a structural formula for the major organic product of each reaction and specify the most likely mechanism by which each is formed. (g) CH3CH2ONa++CH2=CHCH2ClethanolBromo compound N can undergo substitution with nucleophiles X to give mixtures of products O and P as shown below. Explain how this is possible, and suggest an explanation for the observation that the proportion of product P increases with increasing solvent polarity. F N Br X- O X ...X F P
- Suggest a mechanism for the following reaction. Explain why NaB(CN)H3 is preferable to NABH4 as reagent for this reaction. H,N Ono NH NaB(CN)H3Complete 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 OCH33. Propose a reasonable reaction mechanism for the following transformation. محرم H3O+ H₂O OH