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- Draw the major product of this reaction. Ignore inorganic byproducts. Explain please.(Don't use hand raiting please) and please explanation addCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, 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. Probler Drawing Arrows THF Na :Cl:O 'N. NaO C:O Drag To
- Question) Draw the structure of a possible side product from this reaction!Question: Draw the mechanism of the reaction you will complete in lab. Use the proper arrow drawingconvention to show all bond making and bond breaking steps in the reaction. Background info: A substitution reaction takes place when a nucleophile (Nu:) forms a bond with a carbonatom, displacing a leaving group (L).SN2 reactionLeaving groups are typically weak Bronsted bases that are stable as anions (often halide anions).The precise timing of when the leaving group leaves depends on the structure of the substrate –the molecule bearing the leaving group. Methyl and primary alkyl halides tend to undergo SN2type reactions. In this type of reaction, the nucleophile attacks the carbon from the side oppositethe leaving group and the nucleophile-carbon bond is made simultaneous with the carbon-leavinggroup bond breaking. SN2 reactions are one-step and there is an inversion of stereochemistry atthe carbon bonded to the nucleophile.SN1 reactionIf the carbon undergoing substitution is…only answer part D. thank you
- Draw the major organic product or products for the reaction. Multiple products may be drawn in one box, in any order. Include charges as needed. .F HNO3, H2SO4 F.Give detailed Solution with explanation needed..give correct answer if you not then don't give answer..I will give you upvote..draw out all of the substitution and elimination reactionswith the corresponding reaction step. Drag and drop options on the right-hand side to swap positions and match with items on the left. Reordering may cause items on the right- hand side to swap positions. A) B) C) D) Loss of leaving group Proton transfer (acid/ base) Nucleophilic attack Rearrangement OH H. A) OH Br Pr Br Et NaBr/H2SO4 Me + HSO4 Na Pri or Me Et Me Et Br Pr © D) Br Η ΘΗ Н B) c) H -H +0==0 OH H + H₂O III III III III