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- Question 5 1). Draw all resonance structures for the carbocation intermediate formed by para attack; circle the resonance structure that is particularly unstable. N- N Cl₂ AICI 3 H 2). Draw all resonance structures for the carbocation intermediate formed by ortho attack; circle the extra resonance structure that is particularly stable. H a Aer ANSAS C HNO3 H₂SO4The given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"Draw the missing reactant for the following reaction
- Draw the strcutres of the missing reactants, intermediates, or products in the following mechanisms. Include all lone pairs.Step 4a: Classify step. The target product is present, but the reaction is not over. The ethoxide ion has been regenerated. :0: :0: What is the key process in the next step of the mechanism? proton transfer formation of a o bond between nucleophile and electrophile loss of a leaving group carbocation rearrangement (e.g., methyl or hydride shift)Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions below. You may omit NBS in your mechanism, and use Br and Br2.
- Determine the mechanism of nucleophilic substitution of attached reactionand draw the products, including stereochemistry.24. Which product is formed by the reaction ? A) | B) || C) ||| D) IV Br ОН NaH Br ... هستم IVThis question refers to the following reaction: (SEE IMAGE attached FOR REACTION) Using curly arrows show the mechanism for the reaction to give F.