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- 3. Suggest an alkyl halide (A) that could be used to make the following compound.The analgesic acetaminophen is synthesized by treating 4-aminophenol with one equivalent of acetic anhydride. Complete the equation for the formation of acetaminophen. a. Acetaminophen: b. Additional Product pls add the name for both, thanks!Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)
- Give the mechanism and product for the reaction below.Give only typing answer with explanation and conclusion to all parts draw the mechanism for these 4 reactions with electron movement and arrows and products formed The dehydration of 2-butanol with H2SO4 The dehydration of 2-butanol with H2SO4 The dehydrobromination of 1-bromobutane with potassium tert-butoxide The dehydrobromination of 2-bromobutane with potassium tert-butoxideUsing the appropriate reagents and sequence of reactions, propose how you could get 2-Methyl-1,4-pentadiene from Acetaldehyde. Shows the reaction sequence. An important hint, in the synthesis steps you have to performing an oxidation of an -OH to a ketone with CrO3/Pyridine
- Provide the mechanism of the redica reaction below (b)Come up with a reasonable mechanism to explain the following reaction.The reaction of 1-iodopropane with potassium thiocyanate (KSCN) in certain solvents results in the formation of two isomeric products, propylthiocyanate and propylisothiocyanate (see scheme below), via the SN2 reaction mechanism. Attempts to prepare a similar mixture of these same isomeric products (propylthiocyanate and propylisothiocyanate) starting from 1-propene is illustrated below. Despite the strong acidity of thiocyanic acid (recall pKa = 1.1), this addition reaction does not lead to either of the products indicated. Based on your knowledge of alkene addition reactions, explain this experimental result.
- (ii) The elimination reaction between 2-bromobutane and NaOCH2CH3 gives two organic products. Draw a mechanism for the reaction which produces the major organic elimination product and provide a rationale as to why that is the major product.(with explanation)Synthesis of 3-Methylbutyl Ethanoate by an Acid Catalysed Esterification (FischerEsterification) & Purification by Simple Distillation Can you explain the details of what's going on this reaction please Specifics please i'll also leave a good review if you can help thank you4eplease give the resulting product and explain