The dicarboxylic acid, ethanedioic acid, can form a polyamide with 1,2-ethanediamine. To illustrate the growth of the polymer, draw the linear trimer that would form if two ethanedioic acid molecules reacted with one 1,2-ethanediamine molecule.

A polymer is made up of repeated subunits. Refer to the polymer shown to answer the questions. CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 In What is the common name for the polymer? Draw the corresponding monomer. Poly(vinyl chloride) Polypropylene Poly(methyl-a-cyanoacrylate) Polystyrene Polyethylene Polytetrafluoroethylene Polyisobutylene Incorrect H MacBook Pro CMN

Write an equation for the reaction of chloroacetic acid (Ka=1.5103) with trimethylamine (Kb=5.9105) . Calculate the equilibrium constant for the reaction. If 0.10 M solutions of these two species are mixed, what will be their concentrations at equilibrium?

Answer the following questions: 1. Hydrolysis reaction that produces propanol 2. Addition reaction that produces bromobutane 3. Hydrogenation of cyclopentene 4. Complete oxidation of ethane (assuming sufficient O2 is available) 5. Iodation of pentane 6. Production of pentanol from pentane 7. Polymerization of butanedioic acid and propane-1,3-diol (show at least two reactions to get across the idea of growing chain) 8. Esterification of propanol and pentanoic acid 9. Elimination reaction with octanol

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1. a) Use structures to show the formation of an ester via a condensation reaction. Specifically: First draw structures of palmitic acid and methanol Then draw the ester that would form when this acid and alcohol are heated with HCl as an acid catalyst. ● b) In Part A of Lab #7, how will you know that you've successfully condensed the various acid and alcohol functional groups to form ester linkages? c) Which of the condensation reagents do you need to handle with care, and why?