What is the major product (Y) produced in the following sequence of reactions? ů COA B OC E A HO of CI B SOCI₂ Pyridine X CH,OH Pyridine Y D E
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- Draw the organic product(s) of the reaction of phenylacetaldehyde with KMnO4. H3O+Which of the following does not support a nucleophilic attack of a covalent catalysis? a. Hydroxyl b. Sulfhydryl c. Imidazole d. Amino e. MethylWhat products are formed when the following molecule reacts with catalytic H2SO4, H2O, and heat? Please show the mechanism for the reaction.
- When the rate constants for the hydrolysis of several morpholine enamines of para-substituted propiophenones are determined at pH 4.7, the r value is positive; however, when the rates of hydrolysis are determined at pH 10.4, the r value is negative. a. What is the rate-determining step of the hydrolysis reaction when it is carried out in a basic solution? b. What is the rate-determining step of the hydrolysis reaction when it is carried out in an acidic solution?Provide the primary product and the mechanisms of the reaction shown below.Draw the structure of unsaturated carbonyl compound(s) formed when 3-Hydroxy-2,4-diphenyl-butyraldehyde is heatedin i) a basic ii) an acidic solution. iii) Write the complete mechanism for the dehydration reaction that takes place in the basic solution.
- Reduction of an alkyl azide results in the formation of —-. A. an imine B. an oxime C. a tertiary amine D. a secondary amine E. a primary amineSelect the appropriate reagent and TWO possible substrates for the following reductive amination.The first step in the mechanism of reduction of an aldehyde or ketone with either LiAlH4 or NaBH4 is nucleophilic attack. Which of the following is the electrophilic site in this first step?
- What starting materials are needed to synthesize the following azo compound?Draw what compounds would result from complete hydrolysis of the following heterocyclic compound.What is the mechanism of this transformation? Super confused on this mechanism any help is much appreciated Apparently the first step is formation of an iminium cation through the condensation of a primary amine with dihydroxyacetone phosphate.