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- 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 OHWhen treated with NaOH, the bromide below gives an alkene by the E2 mechanism, by eliminationof the circled atoms: (a) Draw the Newman projection from which elimination takes place. (b) Draw the mechanism. (c) Draw the product with the proper stereochemistry. (d) Assign the proper stereochemical descriptor to the product. (Z, E? Trans,CiS?) (e)What would happen to the stereochemistry of the product if the enantiomer of the starting material were used inthe reaction?Provide a mechanism with products for the reaction above. CH3 2Na/Liq.NH₂
- 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 HWhen treated with NaOH, the bromide below gives an alkene by the E2 mechanism, by elimination of the H atom indicated by the arrow: (a) Draw the Newman projection from which elimination takes place. (b) Draw the mechanism. (c) Draw the product with the proper stereochemistry. (d) Assign the proper stereochemical descriptor to the product. (e) Give the rate equationCompound A on ozonolysis yields the two products shown. What is the structure of compound A? Compound A 1.03 2. (CH3)2S ||| ol H H || IV H H
- Alkyl diazonium salts are unstable even at low temperature. They decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products. NANO2 он + HCI, H2O NH2 онPropose a stepwise mechanism for the following transformation. Show curved arrows for each step of the mechanism. Me 1) excess EtMgBr он ||Me 2) H3O*Provide a mechanism for the following reaction. Label every pericyclic process. KF SiMe3 heat OTf
