Draw the major organic product you would expect to isolate from the reaction of p-bromoethoxybenzene with a misture of HNO3HNO3 and H2SO4H2SO4
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Draw the major organic product you would expect to isolate from the reaction of p-bromoethoxybenzene with a misture of HNO3HNO3 and H2SO4H2SO4.
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- Give the main organic product that would form after the following reaction. OMe OMe H₂O H*Wittig reactions with the following -chloroethers can be used for the synthesis of aldehydes and ketones. (a) Draw the structure of the triphenylphosphonium salt and Wittig reagent formed from each chloroether. (b) Draw the structural formula of the product formed by treating each Wittig reagent with cyclopentanone. Note that the functional group is an enol ether or, alternatively, a vinyl ether. (c) Draw the structural formula of the product formed on acid-catalyzed hydrolysis of each enol ether from part (b).What organic product would you obtain from reaction of 1-pentanol with CrO3, H2O, H2SO4?
- 4. Aldehydes and ketones can be “protected" as acetals and ketals. Complete the following outlined reactions, showing how the protection is accomplished, and what results after deprotection. MgCI 1) 2) HO* deprotection hereDraw the principal organic product for the reaction of 1-bromopentane with lithium in diethyl ether, followed by formaldehyde in diethyl ether, and then followed by dilute acid.Ethers can often be prepared by SN2 reaction of alkoxide ions, RO*, with alkyl halides. Which of the two possible routes would be the better choice to synthesize the molecule shown below? Explain briefly.
- 4. Synthesize the following compound. You may use benzene, acetylene, ethanol and any inorganic reagents. O₂NPredict-the-Product. Draw the structure(s) of the major organic product(s) formed in the following reactions. Please indicate stereochemistry where appropriate.The nitro groups on the benzene ring in the reactant serve two purposes.One is to let you know what atoms in the reactant correspond to what atomsin the product. But what role do the nitro groups play electronically – whywould the reaction be much slower if these nitro groups weren’t attached tothose benzene carbons? Draw any relevant structures to support youranswer.
- uo 9:0A Asiacell I. 02:48 المتبقي متعد د الخيارات Which alkyl halide would react the fastest under substitution conditions with HO-? 2-bromo-2-methylpentane O 2-bromo-3-methylpentane 1-bromo-2,2-dimethylpentane 2-bromopentane 1-bromo-4-methylpentane O 1 of 5Draw the principal organic product for the reaction when 2-bromopropane is treated with lithium in diethyl ether, followed by copper(I) iodide and then 1-bromoethane. Click and drag to start drawing a structure. XDraw the structure(s) of the major organic product(s) from the following reactions