What is the synthetic scheme that can be used to produce the target molecule. Pay attention to stero - or regiochemistry. Will require more than two seperate synthetic steps. Clearly explain ? ค ა
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- H₂C H H₁C Br NBS CH, CH₂ CC, hv **You may assume that Br-Br is formed by a side reaction that occurs (which we discussed in class). This is useful for one of the steps of the mechanism.Given the target molecule and it's synthons, propose it's synthetic equivalents and a forward synthesis.Can you draw this multistep synthesis out?
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the intermediate and product in this reaction or mechanistic step(s). Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore inorganic byproducts.Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C. ... NH2 HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one. + 4 n [ ?please draw detailed mechanism. mention which one is the nucleophile, electrophile,base/ acid. Also talk about stereochemistry/ regioselectivity. In terms of stereochemistry why are we getting trans alkene. Why is the trans alkene Produced is it due choosing PPh2 as regeant? Also This reaction is the Horner wadsworth emmond wittig.
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the intermediate and major product of this condensation reaction. Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore inorganic byproducts. :0: Select to Draw Select to DrawAcyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C HCI / H2O `NH2 reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na", I, in your answer. • In cases where there is more than one answer, just draw one. opy aste Previous NextWhat is the complete mechanism for this F!she rxn?