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Predict the products of the following reactions.
ethoxybenzene + concd. HI, heat
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- 9. Draw the structural formulas for the product(s) of each of the reactions below. ("n" indicates "many".) | b) n cIC(CH2)6CCI + n HO(CH2)2OH → |In the reaction given below, what type of reaction is used? n-Pentane → Isopentane нннн H ITH Н—С—с—С—с —О —Н Н—с—с— с-с—н ||| | H нн H Addition Elimination Substitution RearrangementDraw the organic product you would expect to isolate from the nucleophilic substitution reaction between the molecules shown. Note: You do not need to draw any of the side products of the reaction, only the substitution product. + H₂O Cl + ☑ 5 C Click and drag to start drawing a structure.
- Identify the major product of this reaction of an alkene. | ||| OH OH 1. Hg(OAc)2, H2O 2. NaBH4, NaOH || IV ㅊ OH OHDraw structures of compounds that fit the following descriptions: a) An , unsaturated ketone, C9H8O b) An diketone c) An aromatic ketone, C9H10O d) A diene aldehyde, C7H8OComplete the following oxidation reaction by drawing a structural formula for the product. d H CH₂CH3 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. ▶ 85 CH4 +[ ] کر ? ChemDoodle
- Predict the major products of both organic reactions. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products. U + T но X Click and drag to start drawing a structure.2. Provide the reactant, reagents, or products for the following reactions. Br NH₂ $ Phthalimide NaOH, Br₂ H₂O Ag₂O H₂O, ADetermine the product of the following reaction! „H* OH но
- complete the synthesis cyclohexane to 1R,2R 2 bromocyclohexanolH3C CH3 H3C NA C→XT Br Br₂ CH₂Cl₂ H3C Electrophilic addition of bromine, Br₂, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH₂Cl₂. CH3 Br In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br CH3 H3C CH34. What are the products from the following reaction? H3O+ کا