Part 1. Draw monomer units of the following products and draw their reaction mechanism (with arrow pushing) Polyester fiber Using a) pthalic anhydride + anhydrous sodium acetate + ethylene glycol B)pthalic anhydride + anhydrous sodium acetate + glycerol
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- Identify the best reagents to complete the following reaction. Options are included.A student wanted to try to make phenoxyacetic acid using hydroxyacetic acid (HOCH2COOH) and chlorobenzene. His plan was to use NaH to deprotonate both OH groups, and then the more basic alkoxy group would react with the chlorobenzene. Would this procedure work? Explain.Bromobenzne + Mg/diethyl ether -> Biphenyl (byproduct) Draw the mechanism for the byproduct
- HW9 #5Starting with ethene give a suitable reaction scheme to convert it into Ethyl ethanoate in 4 stepsWhich of the following statements is incorrect? Chlorobenzene undergoes EAS reactions faster that methoxybenzene Meta substitution means 1,3-arranged product is formed on benzene An aromatic compounded loses its aromaticity in the first step of EAS Benzene rings require strong electrophiles in order to undergo EAS reactions
- A tosylate is synthesized by reaction of p-toluenesulfonic acid with a(n) __________. amine ester ether carboxylic acid alcohol Cyclohexanol plus chromic acid reagent will yield __________. cyclohexan-1,1-diol cyclohexanone cyclohexan-1,2-diol hexan-1,6-diacidThe diol shown undergoes reactions with reducing and oxidizing agents to yield two different products: A and B. Draw the major organic product for each of the reactions shown. ОН of ОН (A) Reaction with MnO, in propanone at 25 °C. (B) Reaction with KMNO,, HO¯ and heat, followed by 4> an acidic aqueous workup. Select Draw Rings More Erase Select Draw Rings More Erase H C HButanone undergoes a nucleophilic addition with a Grignard reagent made from 1-bromopropane and magnesium metal in THF solution. The alkoxide formed from the nucleophilic addition is then conveted into the final product by the careful addition of dilute acid. Complete the mechanism by following the instructions provided for each step. Step 1. Nucleophilic Addition in THF