_12. What is the most likely product of the following reaction? „NH 1. LIAIH, (excess). 2. H,O° OH OH OH OH II II IV V а. I b. П d. IV е. V с. Ш
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- 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…Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?Predict the product(s) of the reaction below: Al₂O3 → which is it below O2 AI AI + O AI +O2
- According to this video, https://www.youtube.com/watch?v=9Ng6Zv9oLzk, draw the dienophile that was used in the example explaining s-cis and explain what is different about this dienophile from common examples?The replacement of CH3OH to dimethyl sulfoxide, DMSO (CH3)2S=O) as a solvent in the substitution reaction below results in what?In the beginning of this video https://www.youtube.com/watch?v=9Ng6Zv9oLzk, what reason is given on why the dienophile likes the diene?
- For 10.29, the trans product (major product) and the cis product (third product) are displayed as possible E2 products. However, for 10.30, only the trans product (major product) is shown. How come the cis product is not needed?The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.Describe every aspect of the procedure clearly and explicitly. Include temperatures, appearance of the reaction (include pictures!). How is the reaction monitored? Is the order of addition important? 4,4'-DIBROMOBIPHENYL [Biphenyl, 4,4'-dibromo-] Submitted by Robert E. Buckles and Norris G. Wheeler1. Checked by R. S. Schreiber, Wm. Bradley Reid, Jr., and Robert W. Jackson. 1. Procedure In a 15-cm. evaporating dish is placed 15.4 g. (0.10 mole) of finely powdered biphenyl (Note 1). The dish is set on a porcelain rack in a 30-cm. desiccator with a 10-cm. evaporating dish under the rack containing 39 g. (12 ml., 0.24 mole) of bromine. The desiccator is closed, but a very small opening is provided for the escape of hydrogen bromide (Note 2). The biphenyl is left in contact with the bromine vapor for 8 hours (or overnight). The orange solid is then removed from the desiccator and allowed to stand in the air under a hood for at least 4 hours (Note 3). At this point, the product weighs…