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- Draw bith the higher molecular weight prlduct and the lowe weight productPlease help with both questionsA benzene ring alters the reactivity of a neighboring group in the so-called “benzylic” position, similarly to how a double bond alters the reactivity of groups in the “allylic” position. Benzylic cations, anions, and radicals are all more stable than simple alkyl intermediates. a) Use resonance structures to show the delocalization of the positive charge, negative charge, and unpaired electron of the benzyl cation, anion, and radical.
- 1. Consider the SN2 reaction between the two molecules shown: ( in picture) a) Find nucleophile in reaction.b) find leaving group in the reaction.c) Draw the curved arrows indicating the bonds broken and formed in the reaction to correctly show how this mechanism proceeds. d) Draw only the structures of the product(s), including all non-zero formal charges and relevantlone pairs.Curved 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. H ..:OH: Select to Add Arrows HCI H H H H H :CI: OH, Најан Select to Add Arrows !Please don't provide handwritten solution.....
- pls helpDraw a curved arrow mechanism for the substitution reaction that will occur with the alkyl halide and nucleophile below, adding steps as necessary. Be sure to include all nonbonding electrons and all nonzero formal charges, and show all species that react or are formed in this reaction. Cl H₂OConsider this nucleophilic substitution reaction. Part: 0/2 +:CEN: Part 1 of 2 Highlight the electrophilic carbon in red, and highlight the leaving group in blue. Highlight the atom in the nucleophile that will attack the electrophilic center in green. Only atoms need to be highlighted and not the lone pairs or formal charges. + :CEN: G
- 3) Use the reaction shown below and the associated reaction energy diagram to answer the following questions. E A Но- + Br HO. Br- reaction coordinate a) In the space above, use curved arrows to show the mechanism of the reaction. b) Classify the reaction as either addition, elimination or substitution. c) In this reaction is hydroxide (HO-) acting as a nucleophile or as a base? c) Based on the reaction energy diagram, is the reaction endergonic or exergonic? d) Based on the reaction energy diagram, and assuming the reaction is reversible, would the equilibrium lie to the left or to the right? e) Which position on the reaction energy diagram (A, B or C) corresponds to the transition state?ited Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. od m... • You do not have to consider stereochemistry. . Do not include anionic counter-ions, e.g., I', in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom Separate resonance structures using the → symbol from the drop-down menu. ● CH4 + ? HBr1. a) Show the reaction of 3,4,5-trihydroxybenzoate (gallic acetate) with an ORS (oxygen reactive species), in this case use the radical RO•. Draw at least one resonance structure of the radical formed from your compound. b) Draw the resonance hybrid of this stabilized radical.