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6. Maleic anhydride reacts with ethylene glycol to produce an alkyd resin. Draw the structure of...
1. Draw the polymer that would be made from the monomer vinylidene chloride (CH2=CCl2). 2. Draw the structure of the polymer that would be produced from the condensation polymerization of maleic anhydride with ethylene glycol. 3. Draw the structure of the polymer that would be produced from the condensation polymerization of terephthalic acid with 1,4-cyclohexane-dimethanol.
Questions for Experiment 8: Preparation and Properties of Polymers - Polyester and Nylon 1. Which polyester should be theoretically more rigid, the one obtained from ethylene glycol or the one from glycerol? Why? Explain with structural arguments. 2. Draw the structure for the polymer produced from the monomer vinylidene chloride CH-00) 3. Draw the structure of the copolymer produced from vinyl acetate and vinyl chloride. This copolymer is employed in some paints, adhesives, and paper coatings 00CH, CI coc Vinyl...
14. Draw the Lewis structure for ethylene glycol and ethanol. (The skeleton for ethylene glycol is HOCH2CH2OH and ethanol is CH3CH2OH.) Remember to show any lone pairs of electrons. Use your Lewis structures for water, cyclohexane, ethylene glycol, and ethanol to help you answer the following questions below.
Draw a mechanism for an esterification reaction between phthalic anhydride and ethylene glycol under acidic conditions. (I need help seeing how this reaction would occur with a molecule such as phthalic anhydride, thanks!)
Draw a structure for the exo product formed by cyclopentadiene and maleic anhydride. Because the exo form is more stable than the endo form, why is the endo product formed almost exclusively in this reaction? In addition to the main product, what are two side reactions that could occur in the preparation of cis-Norbornene-5,6-endo-dicarboxylic anhydride from cyclopentadiene and maleic acid in the presence of ethyl acetate and ligroin?
diels alder reaction Draw a structure for the exo product formed by cyclopentadiene and maleic anhydride. Because the exo form is more stable than the endo form, why is the endo product formed almost exclusively in this reaction? In addition to the main product, what are two side reactions that could occur in this experiment? The infrared spectrum of the adduct is given in this experiment. Interpret the principal peaks.
Polyethylene phthalate is a copolymer containing phthalic acid and ethylene glycol. Modify the molecules to show the product formed from the condensation of one molecule of 1,2-ethanediol (ethylene glycol) and one molecule of phthalic acid. Select Draw Rings More Erase = atoutus carmens privacy polley terms of use contact us help.
Draw the endo and exo products for the reaction of 1,3(E)-pentadiene with maleic anhydride. Which is the major product?
4) Refer to the following information for parts a -e: Ethylene glycol, C;H.O. (b. is a sweet tasting liquid used as a main component of antifreeze or coolant for cars. The combustion of ethylene glycol is also a key reaction for the formation of polyester. a. What is the empirical formula for ethylene glycol? b. The balanced chemical equation for the combustion of ethylene glycol is shown below. Identity the oxidizing agent and the reducing agent for the reaction. |...
a) a-phellandrene combined with Maleic Anhydride (diels-alder) followed by NaOH produces one product. Treating with NaOCH3, followed by an acidic workup produces a new product. What is it's structure and why is not a good derivative to use to characterize the Diels-Alder product? b) Toluene in used as a solvent in these Diels-Alder reactions. Draw the Aiels-alder products from the reaction of toluene and maleic anhydride. Why is this product not formed during traditional Diels-Alder reactions?