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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- Refer to image, answer all parts and explain. Will rate!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.Refer to image, please answer clearly and explain. Will rate!
- 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.See image belowCurved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the missing reactants/intermediates in this SN1 mechanism. Include all lone pairs. Ignore byproducts. Ignore stereochemistry.
- provided starting structure, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Then draw the organic product of this reaction. Include all lone pairs in the structures. Ignore inorganic byproducts, counterions, and solvents. BroH COH: HH Select to Add Arrows H HBr H HH :Br: O ستمرة HH Select to Add Arrows HBr H Br: O HBr H' HH Drawing H HH HH Select to AddGive only typing answer with explanation and conclusionPlease answer correct
- please do the a new mechanism. which one is the nucleophile/electrophile. And what is Name the reaction. PLEASE Discuss the stereochemistry so why the dash bond go to wedged- is it due to inversion? Please explain.Why is PPh3 used for selectivity ? Please answer all of my questions.Mechanism pleasePredict the organic product for the reaction and complete the arrow pushing mechanism. Please use the steps that are given, this would be incredibly helpful.