For the reaction shown, draw the transient product of one equivalent of reagent adding across the triple bond, and then show the product of a second mole of reagent. 1 mol H2. 1 mol H2, Pt Pt Product A Product B
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- Pls ignore the highlighted part __________ is reduced in thefollowing reaction: Cr2O72- + 6S2O32-+ 14H+→ 2Cr3+ + 3S4O62- + 7H2OReally 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…Please give me the final product following reaction . Feel free to write out each step! thatd be greatly appreciated!
- Can u help pls with a mechanism for one from the three reaction thank uHello please could you help me with the question below? Thank you so muchConsider Table 4 and suggest why FCH2CH2Br (5.7 vs. 1) has a higher SN2 reaction rate than EtBr.(a) Analyze SN1 or SN2 is preferred in the reaction below. Explain your choice and express themechanisms.
- show all important steps of rxn. (3S,4R)-2-bromo-3-propyl-2- phenylpentane in ch3OH. label arrow, intermediates, and all potential priductscmplete the reacting by adding necessrt reagents. write in thapce provided. make sure to write regents in chemical formula . n separate regents with comma & space (ex. h2so6, h202)Can you draw the products that form when 1-butene reacts with; O3, then Me2S OsO4, then NaHSO3/H2O Br2 in H2O Please analyze in detail for each. Also can you please reply fastly?
- Predict the product for each one clearly Please answer fast I give you upvoteWhy does the final product has the opposite configuration compared to the reactant? Shouldn’t it form OMs first, then OMs gets substituted by Cl- via Sn2 (the 1st inversion of configuration) then the Cl- gets substituted by OCH3- (the 2nd inversion of configuration? To my understanding 2 inversions = same configurationPlz solve product with mechanism plzz explain