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What will the major product of this reaction be? Please explain why the correct answer is letter E. Include detailed steps and a drawing explaining the mechanism of the reaction.
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- 2. Indicate the reagents and draw the intermediate products necessary to accomplish the following transformations. of (a) HO, (b) -CN CI (c) но7 Draw the structure of the product, substrate or condition in the following reactions (should clearly indicate the stereochemistry). (a) Mẹ 1) Os04 2) NaHŠO3 (b) 1) (sia)2BH 2) NaOH/H2O2 H2O (c) Он (d) Br2 Br Н ÕH1. Provide (a) a plausible mechanism for the following reaction which will form both products: .CI + (b)State the reagents necessary for the reaction to occur (c) State the byproduct (d) Name both major products 2. Choose ONE of the major products from question 1 and (a) draw a mechanism for the chlorination of the methyl group. (b) provide the reagents (c) provide the products
- Reaction of this bicycloalkene with bromine in carbon tetrachloride gives a trans dibro- mide. In both (a) and (b), the bromine atoms are trans to each other. However, only one of these products is formed. CH3 CH3 CH3 Br Br CH,Cl, + Br2 or Br Br (a) (b) Which trans dibromide is formed? How do you account for the fact that it is formed to the exclusion of the other trans dibromide?Predict the major products of the following reactions. If it is possible, write all stereoisomers.What will the major product of this reaction be? Please explain why the correct answer is letter E. Include detailed steps and a drawing explaining the mechanism of the reaction.
- (c) Compound 2F shown below is a tetra-substituted cyclooctatetraene. After heating 2F at 160 degree for 6 hours, researchers observed the formation of an isomer of 2F. Draw the isomer structure and provide a plausible mechanism to explain the formation of the isomers. 2FPredict the product(s) and provide the mechanism for each of the following reactions. (a) (b) LOCH₂CH3 HI HBr ? ?Kindly answer this question
- 7В. (2 Draw the structure of the product, substrate or condition in the following reactions (should clearly indicate the stereochemistry). (а) OH (b) OsO vaHSO3 (c) 1) (sia)2 BH 2) NaOH/H,O2 H20 (d) HBr (2 equiv) Br, Br Hint: This is the only product formed (e) Br Br2 H20 OH (f)(a) Beginning with 100% (R)-2-chlorobutane, upon reaction with NaOH in polar aprotic solvent, what is the major product? OH (b) OH (c) a racemic mixture of a and b (d) there is no reactionGive the product (b) of the synthesis shown.