Where is there the highest build-up of partial positive charge in the following alkyl halide? Br O At the bromine O At the carbons with the pi bond At the carbon attached to the bromine All the carbons have the same partial positive charge
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- Tautomerization is a process in which an enol yields a ketone Give one examplefor a keto to enol tautomerization. Which form is more stable. Also, which ismore stable the E isomer or the Z isomer of 2-Chloro, 2-ButeneSubject the resulting alkyne (attached picture) to the following reactions (show also the steps and the reagents needed in the steps): Hydration with borane Halogenation with bromine (2 molecules of bromine are given)When a carboxylic acid is dissolved in isotopically labeled water, the label rapidly becomes incorporated into both oxygen atoms of the carboxylic acid. Explain.
- Please Complete the following reaction with Major Compund with explaination in handwritten....r Plase don't provide handwritten solution Write carbonyl compound & phosphonium ylide that yield below alkene upon reactionSubject the resulting alkyne above to the following reactions (show also the steps and the reagents needed in the steps): Hydrohalogenation with HCl (only one HCl is given) Hydration with borane
- Compounds A, B, and C have the same molecular formula C4H8. They all react wotu H2/PtO2 to give the same compound. The reaction of A or B with H2O/H2SO4 or with BH3-THF, followed by treatment with a basic solution of hydrogen peroxide, gives the same compound, namely D. The reaction of C with H2O/H2SO4 also gives D. However, the reaction of C with BH3-THF, followed by HO-, H2O2 gives a new compound, E. Provide the identity of A, B, C, D, and E along with explanations of reactivity.The following group are ortho-para director.Draw a contributing structure for the resonance-stabilized cation formed during electrophilic aromatic substitution that shows the role of each group in stabilizing the intermediate by further delocalizing its positive charge.Identify the major organic product for the following reaction
- Draw the mechanism of the hydration and the enol ketone tautomerization reaction using one of the alkynes in calicheamicin. Use the formal arrow pushing formalism and show the product of this hydration."The following reactions DO NOT afford the product that is shwon. Concisely explain why this is so."