1. Polyester Formationa. Draw the structure of the polyester formed (Seabacoyl Chloride + EthyleneGlycol).(Insert scanned hand-drawn structure or ChemDraw image.)b. What molecules are eliminated in this condensation reaction?

Step 1: Step 2: Step 3: Step 4:

Answered: 1. Polyester Formation a. Draw the…

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter16: Amines And Amides

Section: Chapter Questions

Problem 16.52E: Complete the following reactions: a. b.

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A. Identify at least one nylon with a structure other than the nylon used in lab. i. Provide the repeating molecular structure of the fiber ii. Provide the structure of the carboxylic acid or carboxylic acid derivative that can be used to make the fiber iii. Provide the structure of the amine that can be used to make the fiber iv. Identify materials or applications where this fiber is used. If the fiber investigated is novel and has not been used in a commercial material yet, what are the proposed uses of this material? Why is it being investigated? (
2. Explain why styrene is soluble in toluene, but not in ethanol.
Complete the following reactions: a. b.
Which of the following reacts fastest in nucleophilic addition reaction? a. Acetic acid b. Ethanol c. Formaldehyde d. Benzaldehyde e. Acetone How can a water insoluble acid be converted into a water soluble compound? a. By reacting it with an alcohol. b. By reacting it with hydrochloric acid. c. By reacting it with nitric acid. d. None of the mentioned method. e. By reacting it with sodium bicarbonate
A) the possible methods to purify cyclohexene from cyclohexanol and other materials produced in the reaction. B) explaining why distillation is an ideal choice
1. Why is it that muriatic acid is packed in plastic container, while Acetone is usually in glass bottles? Explain while applying the chemical principles learned.
Chemistry Please answer the following two questions. 1.) Why are functional group interconversions controversial? (double bonds into epoxide) 2.) Explain the clincal trials that happen for epoxide containing molecules
Por the organic product of the reaction below.. 1.) NaH 2.) Br HO, a.) b.) c.) of Na d.) e.) Br (Racemic)
Hydrocarbons like benzene are metabolized in the body to arene oxides, which rearrange to form phenols. This is an example of a general process in the body, in which an unwanted compound (benzene) is converted to a more water-soluble derivative called a metabolite, so that it can be excreted more readily from the body.a.Classify each of these reactions as oxidation, reduction, or neither. b. Explain why phenol is more water soluble than benzene. This means that phenol dissolves in urine, which is largely water, to a greaterextent than benzene.
a.) Look up the structure of salicylic acid and the structure of acetic anhydride. Indicate where the two molecules would attach to form aspirin (acetylsalicylic acid). See if you can predict the remaining product in the synthesis. b.) What carboxylic acid and what alcohol react to produce propyl acetate (pear flavoring/smell)?
These compounds are unreactive to NaNH2 EXCEPT a. 1-butene. b. 2-butyne. c. 2-butene. d. 1-butyne.
5. Nomenclature following molecules. a. 2. Cu ts). Draw the appropriate structure and provide an IUPAC name for the 3-(N-methylamino)propanoic acid b. m 'N H

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