Predict the FINAL product for the following synthetic transformation: NH2 HNO3 H3O+ H2SO4 ? A B 0 NH2 NH2 NH2 O₂N O₂N A B C D NO2 NO2 D NH2 2 NO2
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- When cis-2-decalone is dissolved in ether containing a trace of HCl, an equilibrium is established with trans-2-decalone. The latter ketone predominates in the equilibrium mixture. Propose a mechanism for this isomerization and account for the fact that the trans isomer predominates at equilibrium.Identify A, B, and C, intermediates in the synthesis of the five-membered ring called an α- methylene-γ-butyrolactone. This heterocyclic ring system is present in some antitumor agents.Please explain steps on how to get each product.
- Identify A, B, and C, intermediates in the synthesis of the ve-membered ring called an α-methylene-γ-butyrolactone. This heterocyclic ring system is present in some antitumor agents.Reaction of phenol with acetone in the presence of an acid catalyst gives a compound known as bisphenol A, which is used in the production of epoxy and polycarbonate resins Propose a mechanism for the formation of bisphenol A. OH H;PO, + H,O НО HO Phenol Acetone Bisphenol APropose a plausible mechanism for the following transformation: 1) Excess MeMgBr 2) H₂O HO
- Select the correct reagent for the following transformation O H2/Pt O XS LAH O PCC O NaBH4 O Na2Cr207, H2SO4, H2O OHWhich of the following compounds undergoes the most rapid nucleophilic substitution with amide ion? A, B, C, or D?When pent-1-ene is treated with mercury(II) acetate in methanol and the resulting product is reacted with NaBH4, what is the primary organic compound which results? 1-ethoxypentane 1-methoxypentane 3-ethoxypentane 2-ethoxypentane 2-methoxypentane