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A, B and C please
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- 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 is the major difference between catalytic reduction and non-catalylic reduction techniques?3 Give mechanisms for the acid-catalyzed and base-promoted alpha-halogenation ofketones. Explain why multiple halogenations are common with basic catalysis andgive a mechanism for the haloform reaction
- Write mechanism of halogenation of benzene and explain each step of reactionGive detailed answer- Provide example of compound that fulfil each criteria below. Explain why-A)1,2-disconnectionB)1,4-disconnectionC)1,5-disconnectionD)1,6-disconnectionDiscuss comprehensively the basic steps involved in the production of organic acid discussed with you in the online mode of classes?
- Given the sequence of reactions shown below assume the reactions are stoichiometric fill in the reagents needed for steps A B and C and explain what happens in each step of the reactions, by also nameProvide the conditions and show the curved arrow mechanism and Intermediate for the reactions leading to 1 or 2 selectivelyWrite the reaction of 1-bromopentane with sodium ethoxide and show all possible products (E2 and SN2) that could occur. Please don't give handwritten e
- i need help writing all of the detailed methods: in Preparation of Cyclohexanone by Hypochlorite OxidationRepresent the reaction equation of the alkene supplied to you with propanol, in acidic medium, indicating thestereochemistry of all the products formed.An unknown hydrocarbon G, whose formula is C16H26 contains two triple bonds. Ozonolysis followed by reduction with (CH3)2S gave CH3(CH2)4CO2H and HO2CCH2CH2CO2H as the only products. Suggest a reasonable structure for compound G.