Chapter 23: Q66. (page 924)
Question: Synthesize (Z)-hept-5-en-2-one from ethyl acetoacetate (CH3COCH2CO2Et ) and the given starting material. You may also use any other organic compounds or required inorganic reagents.

Short Answer
Answer

Chapter 23: Q66. (page 924)
Question: Synthesize (Z)-hept-5-en-2-one from ethyl acetoacetate (CH3COCH2CO2Et ) and the given starting material. You may also use any other organic compounds or required inorganic reagents.

Answer

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Question: The cis ketone A is isomerized to a trans ketone B with aqueous NaOH. A similar isomerization does not occur with ketone C. (a) Draw the structure of B using a chair cyclohexane. (b) Label the substituents in C as cis or trans, and explain the difference in reactivity.


Question:The enolate derived from diethyl malonate reacts with a variety of electrophiles (not just alkyl halides) to form new carbon-carbon bonds. With this in mind, draw the products formed when Na+ –CH(CO2Et)2 reacts with each electrophile, followed by treatment with H2O.
Question: Draw a stepwise mechanism for the following reaction.

Question: Draw the products formed (including stereoisomers) in each reaction.
Question: 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.

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