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- Please 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.2. A 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. R .R allylic position benzylic 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.
- What type of alkene is Compound X? (Use all reaction information to solve for Compound X's structure.)Draw 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.1. 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.
- Draw a curved arrow mechanism for the reaction. Add steps as necessary and be sure to add lone pairs and charges where relevant. :Br: میں شیدBe sure to answer all parts. Write a second resonance structure for the following carbocation. ✪ draw structure Is the charge shared equally by both allylic carbons? If not, which one bears more of the charge? (select)a) Write out the 3-step arrow pushing mechanism showing how 1-pentene is hydrated to make 2-pentanol. b) Draw the other 2 alkenes(don’t forget cis/trans isomers!) that could also be hydrated to make 2-pentanol. Briefly explain why1-pentene is the best choice.
- Draw the following molecule after it undergoes a chair flip.Draw Resonance Structure of the following cation. Draw curved arrows to indicate the movement of electrhs. A InstructionsUse the curved-arrow formalism to show how the electrons flow in the resonance form on the left to give the one on the right. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Arrow-pushing Instructions Submit Answer m H Try Another Version 2 item attempts remaining a Use curved arrows to show how the alkene below will react with HCI. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Arrow-pushing Instructions NA ↔XT H H