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- Consider the series of the trans effect: CO, CN-, C2H4 > PR3, H-, CH3- > C6H5- > NO2-, SCN-, I- > Br- >Cl- > py > NH3 > H20 What would be the major product of the following reaction? Select one:(a) Analyze SN1 or SN2 is preferred in the reaction below. Explain your choice and express themechanisms.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?
- 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 aboveThe following reaction has a ΔSsystem < 0 O2(g) → 2O(g) T or F can you explain why this is false?select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4
- Which compounds from 5a-d will react with hydroxide in the fashion shown. Which reaction will be the fastest and slowest? Explain using knowledge of carbonyl chemistry, pka and leaving groups.What reagent(s) is needed to complete the transformation below? Options: BH3, then NaOH/H2O2 HBr with peroxides (ROOR) Br2 in H2O Br2 in HOCH3List the following compounds in order of reactivity towards MeOH (1 = highest, 4 =lowest) and propose a quantitative explanation why.
- [III1] Instructions: Add curved arrows to the following reactions to indicate the flow of electrons in each reaction below. Identify and label the nucleophile and electrophile. (refer to the photo below)What is the product (A, B, C, or D) of the reaction shown in Image30? a. C b.D c. B d. AProvide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the help