5. Ethanedioic (oxalic) acid is found in certainvegetables, such as spinach. Ethane-1,2-diol is atoxic synthetic compound better known as ethyleneglycol.0 010-C-C-OHethanedioic acidOH OHHC-CHethane-1,2-diolDraw three units of the polymer made fromethanedioic acid and ethane-1,2-diol.

Carboxylic acid reacts with alcohol to form an ester in the presence of an acid catalyst, the…

5. Ethanedioic (oxalic) acid is found in certain vegetables, such as spinach. Ethane-1,2-diol is a toxic synthetic compound better known as ethylene glycol. OH OH 0 0 10-C-C-OH HC-CH ethanedioic acid methane-1,2-diol Draw three units of the polymer made from ethanedioic acid and ethane-1,2-diol. C

5. Ethanedioic (oxalic) acid is found in certain vegetables, such as spinach. Ethane-1,2-diol is a toxic synthetic compound better known as ethylene glycol. OH OH 0 0 10-C-C-OH HC-CH ethanedioic acid methane-1,2-diol Draw three units of the polymer made from ethanedioic acid and ethane-1,2-diol. C

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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The plastic known as PETE (polyethyleneterephthalate) is used to make plastic soft drink bottles and containers for salad dressing, shampoos, and dishwashing liquids. PETE is a polymer of terephthalic acid and ethylene glycol. Today, PETE is the most widely recycled of all the plastics. After it is separated from other plastics, PETE can be used in polyester fabric, door mats, and tennis ball containers. In 2015, 1.84×109 lb1.84×109 lb of PETE bottles were recycled in the U.S. The density of PETE is 1.38 g/mLg/mL. If 2.74×109 kg2.74×109 kg of PETE bottles were sold in 2015, what percentage of those bottles were recycled? Express your answer to three significant figures.
Alkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.
Alkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.