Determine the major organic product for the reaction scheme shown. H3C-CI 1.2 Li, Et₂O 2. CH3CH₂-C=CH 3. (CH3)2CH(CH₂)2CI Select Draw с Rings H More
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- Complete the following reactions with the majority products and the missing reaction conditions. Indicate stereochemistry if applicable. Also indicate the type of reaction that took place (SN1, SN2, E1, E2, E1bc)The synthesis above can be performed with some combination of the reagents listed below. Give the necessary reagents in the correct order. Be sure to consider stereochemistry and regiochemistry.A. NaOHB. mCPBAC. OsO4, tBuOOHD. NaHE. H2, LindlarF. CH3CH2CH2BrG. CH3CH2ClH. NaNH2I. H3O+J. Na, NH3(l)When 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.
- Please show the reaction for the Alkene Halogenation and Explain each step in the reaction in great detailPlease identify priorities of functional groups and name following molecules based on thier stereochemistry as R or SBenzene is one of the compounds used as octane enhancers in unleaded gasoline. It is manufactured by thecatalytic conversion of acetylene to benzene: 3C2 H2(g) ⇌ C6 H6(g). Which value of Kc would make this reactionmost useful commercially? Kc ≈ 0.01, Kc ≈ 1, or Kc ≈ 10. Explain your answer
- Please complete reactions in clear handwritten of all subpartsWhat is the most likely product, I, II, III, IV, of the following reaction with correct stereochemistry?The reaction of 2-ethyl-1-pentene with Br2, with H2 + Pd/C, or with R2BH/THF followed by aqueous HO- + H2O2 leads to a racemic mixture. Explain why a racemic mixture is obtained in each case.
- Give the structure of the alkene that yields on ozonolysis: CH3CH2CH2CHO and HCHO Only acetone Only OHC-CH2CH2CH2-CHO CH3CHO and HCHO and OHC-CH2-CHOGive to all parts? (a) Give the complete mechanism for the reaction of trans-2-butene with Br2 in excess H2O. (b) Name the products (including stereochemistry). (c) Give the complete mechanism for the reaction of trans-2-butene with Br2 in excess H2O. (d) Name the products (including stereochemistry).For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation. cyclodecyne