ow Attempt History V Your answer is correct. What is the predicted product for the reaction shown? H20 / H2SO4 "H9SO4 HO H. II IV O III IV %3D - = =2 >
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- In light of your answer to Problem 30-40, explain why a mixture of products occurs in the following reaction:EXP VIDEO https://www.youtube.com/watch?v=9Wxxv7kwXlA&list=PLE-217H0ao60Uzpzj-FNP_0ScVp5SZB7j&index=8 1.Pre lab question What are the functional groups in your substrate? -Nitrate -Nitrate and acetate -Amide and ether -Benzene ring b.The stable reaction intermediate in this reaction is Nitronium ion Benzonium ion Carbocation Carbanion c.How would you distinguish between 2-nitrophenacetin and 3-nitrophenacetin? -Color difference -Melting point difference -Difference in Molecular weight -They cannot be differentiated. dAn ether group is -Ortho para activating -Meta activating -Ortho para deactivating -ring activator eThe catalyst in this experiment was -Glacial acetic acid -Nitric acid -Sulfuric acid -Ethanol fThe chemical waste from this experiment should be discarded in the -Sink -Halogenated waste container -non-halogenated waste container -Heavy metal waste container. gWhat is the limiting reagent in this experiment? -Nitric acid -Glacial acetic acid -Phenacetin…Predict the major product(s) and provide a mechanism for the reaction below. Includestereochemistry.
- An inexperienced graduate student treated dec-5-ene with borane in THF, placed the flask in a refrigerator, and left for aparty. When he returned from the party, he discovered that the refrigerator was broken and that it had gotten quite warminside. Although all the THF had evaporated from the flask, he treated the residue with basic hydrogen peroxide. Tohis surprise, he recovered a fair yield of decan-1-ol. Use a mechanism to show how this reaction might have occurred.(Hint: The addition of BH3 is reversible.)It's ET2CuLi sorry haha!! I just would like to know what the major product would be! Thanks sm!Need help ASAP pls & thank you! "Provide the stable organic product(s) for the reactions below."
- As reaction of (CH3)2CO with LIC≡CH followed by H2O affords compound D, which has a molecular ion in its mass spectrum at 84 and prominent absorptions in its IR spectrum at 3600−3200, 3303, 2938, and 2120 cm−1. D shows the following 1H NMR spectral data: 1.53 (singlet, 6 H), 2.37 (singlet, 1 H), and 2.43 (singlet, 1 H) ppm. What is the structure of D?Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)The following reaction has a ΔSsystem < 0 O2(g) → 2O(g) T or F can you explain why this is false?