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- Phenols (ArOH) are relatively acidic, and the presence of a substituent group on the aromatic ring has a large effect. The pKa of unsubstituted phenol, for example, is 9.89, while that of p-nitrophenol is 7.15. Draw resonance structures of the corresponding phenoxide anions and explain the data.please explain how to get thrree answers to thr following questions thanks. Need all threeCan u help me im a student w this problem.
- Really hoping for solutions since I’m having a hard time with this. Pls. skip if unsure or not willing to answer the subitems (these are all connected for one item). Thanks in advanced. A kinetics experiment was performed for the formation of a novel compound, UNO, from its reactants, Chemicals G, R, A, D, and E. The first six runs (Runs 1-6) were all performed at 301 K, while the next two runs (Runs 7-8) at varying temperatures. These are tabulated in the table shown below. Table 1. Reaction rate for the reaction of the different chemicals at a given concentration at 301 K. Run [G], M [R], M [A], M [D], M [E], M Rate, M/s 1 0.80 0.01 0.20 0.50 2.00 0.180 2 0.80 0.02 0.20 0.50 0.02 3.54 x 10-3 3 0.80 0.01 0.20 0.50 0.02 1.80 x 10-3 4 0.80 0.01 0.60 0.50 0.02 1.80 x 10-3 5 1.20 0.01 0.20 0.50 0.02 4.02 x 10-3 6 0.80 0.01 0.20 0.15 0.02 1.95 x 10-2 a. Calculate the rate order of each chemical and overall rate order of the…Explain why ethene does not react with HX ( X=Cl , Br or I) under normal conditions.The following reactions are unlikely to provide the indicated product in high yield. What is wrong with each?
- Isoleucine, another of the twenty amino acids found in proteins, is metabolized by a pathway that includes the following step. Propose a mechanism.Use your knowledge of directing effects, along with the following data, to deduce the directions of the dipole moments in aniline and bromobenzene.predict the products: XCL2+ E3PO4 --->
