6. Which set of reagents would be the best choice to accomplish the transformation shown below? * (1 Point) OH H2O, H2SO4 СНЗОН, Н2SC4 Н2О/Н202/NaОН 1. BH3/THF 2. HO-H2O2, H20 1. NaBH4 2. H30+
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- exolain how to solve trial one so i can do the remaining trials on my own. thanks1. Which of the following is the strongest nucleophile? Refer to the diagram below with an MeOH, MeSH, etc. 2. Which of the following is true about the stereochemistry of SN1 reaction?a.retention of configuration at the electrophilic centerb.50:50 mixture of retention and inversion of configuration at the electrophilic centerc.inversion of configuration at the electrophilic centerd. slightly more inversion than retention at the electrophilic centerA concerted, one-step reaction is involved between tert-Butyl bromide and sodium hydride at 50 o C.True or False?
- Show an actual arrow-pushing mechanism for the transformation below, and briefly explain the observed regioselectivity.Rearrangements can occur during the dehydration of 1° alcohols eventhough no 1° carbocation is formed—that is, a 1,2-shift occurs as the C—OH2+ bond is broken, forming a more stable 2° or 3° carbocation, asshown in Equation [1]. Using this information, draw a stepwisemechanism for the reaction shown in Equation [2]. We will see anotherexample of this type of rearrangementFor each reaction indicate the predominant mechanNism: SN 1, S 2, E1, or E2
- Why arent part 1 and 3 E2 reactions? Doesnt E2 have strong bases as a part of their mechansim?(True/False) The use of sodium iodide in acetone promotes SN2 mechanism for alkyl halide resulting in the formation of insoluble salts in the mixture. (True/false) For alkyl halides, we use a solution of AgNO3 in ethanol because ethanol is a polar protic solvent suited for SN1 mechanism. (True/False) 1-bromobutane, 2-bromobutane (aka sec-butyl bromide), tert-butyl bromide, benzyl chloride, and bromobenzene will not form precipitates in either 1M NaI/acetone and 2% AgNO3/EtOH.1-ethylcycloheptene + cold, dilute KmnO4
- Which reactions will proceed faster in a polar, aprotic solvent? (CH3)2CHCH2I+Na+N3−(CH3)2CHCH2I+Na+N3− (CH3)3CBr+HSCH2CH3(CH3)3CBr+HSCH2CH3 CH3CH2CH2Br+Na+CN−CH3CH2CH2Br+Na+CN− (CH3)2CHOSO2CH3+HOCH(CH3)2On a single graph, draw the reaction coordinate diagram for the addition of one equivalent of HBr to 2-methyl-1,3-pentadiene and for the addition of one equivalent of HBr to 2-methyl-1,4-pentadiene. Which reaction is faster?Which of the following would accomplish the transformation below? a) 1. HSCH2CH2SH, H+; 2. H2, Raney Ni b) H2N-NH2, NaOH(aq), heat c) H2, Pd d) All of the above