Draw the structure of oxidised anthraquinone-2-sulfonate and the reduced structure of anthraquinone-2-sulfonate at both ketone groups taking into accout that 2 protons and 2 electrons are transferred.
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Draw the structure of oxidised anthraquinone-2-sulfonate and the reduced structure of anthraquinone-2-sulfonate at both
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- Explain this difference in potency and speed of onset by pointing out the main differences in functional groups between morphine and heroin.In the separation of hydroquinone dimethyl ether, 2-naphthol and benzoic acid, removing the proton from benzoic acid causes the compound to: Dissolve in the water layer Form a crystal Become more acidic Dissolve in the ether layerIs it possible to do a ring closure between an enamine and ketone on the same molecule? If so what conditions would permit that? Thank you
- In an attempt to synthesize compound C through a two-step process, a chemist discovered after completing the first step that they had inadvertently produced two distinct compounds, A and B. Upon examining the infrared spectroscopy (IR) results, it was observed that both A and B exhibited peaks indicative of a ketone and an ester group. Please provide the molecular structures of A and B. OEt NaOEt ΕΙΟ A B In a chemical experiment, they noticed that both components, A and B, from a combined sample turned into a new compound, C, during the following stage. The task is to determine what compound C looks like and explain how compound A or B changes into compound C through a reaction. Compound C should be the primary molecule containing carbon created in this process, not just a by-product. A B H3O+, H₂O, A Mechanism = сdescribe how steric and electronic effects influence the postion of equilibrium when the electrophilic center of an aldehyde or ketone is under nucleophilic attack.Although ibuprofen is sold as a racemic mixture, only the S enantiomer acts as an analgesic. In the body, however, some of the R enantiomer is converted to the S isomer by tautomerization to an enol and then protonation to regenerate the carbonyl compound. Write a stepwise mechanism for this isomerization.
- Isopulegol is formed as a single stereoisomer. Account for the fact that only a single stereoisomer is formedHow many non-equivalent carbons exist in the following compound? (Give a number) -CEC-Explain why an optically active solution of (R)-α-methylbutyrophenone loses its optical activity when dilute acid is added to the solution.