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- What would the major organic products of these reactions be? Give solution asapPredict the organic products of the reaction of 2 butene with each reagent. Be sure to indicate stereochemistry and regioselectivity where appropriate. a. Br2 in H2O b. Hg(OAc)2, H2O c. Product from (b) + NaBH4What is the reaction when trans-2-butene reacts with 1.KMnO4/-OH in cold 2. hotKMnO4/-OH 3.HBr in the presence of peroxide
- Chemistry What is the final product for the following reactions? Show the stereochemistry if needed.In which of the statements given below, the event is not an oxidation reaction? A. Product formation as a result of the reaction of benzoine with nitric acid B. Formation of the product as a result of the reaction of 2-propene at KMnO4 / Basic ambient temperature C. Formation of the product as a result of the reaction of 2-propene in KMnO4 / Basic medium cold D. CH3CH2OH + KMnO4 → CH3COOH E. Reaction of an alkyl halide with ammoniaWhat are the final products for these reactions? *mechanisms not necessary
- What would the final products look like? Pls specify stereochemistry if neededExcept for one, all of the following statements concerning anthracene are correct which is:a. In Baeyer's test, it returns a negative result.b. A yellow, smoky, sooty flame is produced.c. In cold H2SO4, it is insoluble.d. Under dark conditions, it reacts with bromine. EXCEPT for one 2,3-dimethylheptane and 2,3-dimethylhepta-1,5-diene, the following tests or reagents could distinguish them.a. Under gloomy conditions, Br2 in waterb. Alkylation Friedel-Crafts Testc. CombustionHow many products are obtained following a monochlorination reaction (Cl2, UV) if the stereochemistry is not taken into consideration?
- 1. Write the complete thermal reaction mechanism to get the compound below. Briefly explain every step. Include starting material, reagents used if there are any and indicate conditions. 2. Write the complete thermal reaction of the compound below with buta-1,3-diene. Indicate reagents and conditions. Provide short explanation every step.Choose the best reagent(s) for carrying out the conversion of the reaction below:1. What is the function of CH2Cl2 in the bromination reactions? Why can it fulfill this role?2. In not more than three (3) sentences, explain why terminal alkynes are acidic.3. What impurities are removed when acetylene gas is made to pass through an acidified solution of CuSO4?4. Explain the difference in the rate of free-radical bromination reactions of toluene and cyclohexane.5. Give the reagent or chemical test that would differentiate the following pairs o fcompounds. Provide only the reagents or chemical tests discussed in the module. Write chemical equations for the reactions involved. a. benzene and ethylbenzeneb. 1-butyne and 2-butynec. 2-methylpentane and 2-methyl-2-pentened. toluene and 1-methylcyclohexene