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- Identify F in the following reaction sequence. F was converted in several steps to the antidepressant paroxetine (trade name Paxil; see also Problem 9.9).Please draw the mechanism (assuming an SN1pathway) for the reaction of cyclopentyl bromide with the cyanide anion (-CN) to yield cyclopentyl cyanide as the organic product Thank youDraw a stepwise mechanism for the attached reaction that illustrateshow two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reactionconditions, even though it is a 1 ° alkyl halide.
- Complete the reaction by drawing the reactions major organic product and propose a detailed mecanism for it's formationPlease Answer the following question with proper explanation and mechanism with Chemdraw!Draw the product of this reaction and states its IUPAC name, and states what type of mechanism is occuring (eg. SN1, SN2, E1, E2, etc)?
- . Complete the following reaction schemes using appropriate reagent(s) and predictproduct eGive the complete mechanism with arrows and the molecules below.The reaction of cyclohexene with iodobenzene under Heck conditions forms E, a coupling product with the new phenyl group on the allylic carbon, but none of the “expected” coupling product F with the phenyl group bonded directly to the carbon–carbon double bond. Draw a stepwise mechanism that illustrates how E is formed.
- Please draw the complete mechanism for the reaction below(A) Provide the major organic product for the reaction below (B) Would the product be optically active of optically in active?I need an explanation on the mechanism, linked bellow 1 paragraph explanation on the steps and mechanism. and what the final product is called