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- 6) Give the products of each of the following reactions. a) b) d) H Li, NH3 CH3CH₂OH xo Na₂Cr₂O7 H₂O, H₂SO4, A H₂O LI, NH3 CH₂CH₂OHComplete the following reactions, clearly indicating regio-and stereochemistry where applicable. In cases, where ortho-and para-products are formed, draw both.give the major products of this reaction. include stereochemistry as appropiate. strongly appreciate it.
- 3) Draw the structures of the major organic product(s) for the following reactions. HI in CH₂Cl₂ 3 excess Cl₂ in H₂O H₂SO4 in H₂O (Two products) Br-Cl in THF 1) BH3 2) alkaline H₂O₂ OSO4 + HOOHGive the major organic product of the following reaction for a) or b)what is the structure of the substitution product in the following reaction and consider stereochemistry in deciding your product?
- When treated with NaOH, the bromide below gives an alkene by the E2 mechanism, by elimination of the H atom indicated by the arrow: (a) Draw the Newman projection from which elimination takes place. (b) Draw the mechanism. (c) Draw the product with the proper stereochemistry. (d) Assign the proper stereochemical descriptor to the product. (e) Give the rate equationDraw the product formed by the reaction of t‑butoxide with (1R,2S)‑1‑bromo‑2‑methyl‑1‑phenylbutane. Draw the correct stereoisomer of the product.When 2-iodo-1,4-dimethylcyclohexane is heated in acetic acid, CH3COOH, a mixture of substitution and elimination products is obtained. Provide structures for all possible products, writing [not drawing] the name of the mechanism by which each one is formed.