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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- Cart 2. Predict the products of the follwing reactions. a) Phenol + acetic anhydride b) Phenol + acetic formic anhydride c) Aniline + phthalic anhydride d) o-Methoxytoluene + scucinic anhydride and aluminum chloride e) PHCH(OH)CH2NH2 +1 eq. of acetic anhydride f) PHCH(OH)CH2NH2 + excess acetic anhydride Dr. Gupta/Carboxylic Esters-Synthesis and Reactions-SS/PageA 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.Synthesis of Nefidipine from benzaldehyde and alkene derivative . Preferably use structures
- Choose the best solvent for an SN1 reaction.An organic chemistry experiment involves a nucleophilic substitution (SN2) reaction using 1-iodobutane and 2-naphthoxide ion. The 2-naphthoxide ion is generated from 2-naphthol and sodium hydroxide in an ethanol solvent. The experiment includes steps like generating the nucleophile, conducting the SN2 reaction, and analyzing the product using 1H NMR spectroscopy. Question: Write the structure of the undesired side product if CH3CH2O‾ (ethoxide) reacts with 1-iodobutane.which one is limiting reagent？？
- Which is the MAJOR product of the following reaction? Et 1) BH3:THF 2) H2O2, NaOH Which of the following best describes a key step in the mechanism for the reaction below? HO ... CH3 -CH3 dihydroxylation + en H3C- H3C- HO. electrophilic addition reaction to form a carbocation intermediate B nucleophilic attack by an alkene to form a cyclic (epoxide) intermediate elimination reaction by abstraction of a beta-hydrogen D free-radical substitution at the carbonyl carbon Which alkene will produce the HIGHEST yield of the alkyl halide below? Br. alkene HBr |Which of the following compounds can be used to synthesize ethanoicpropanoic anhydride (CH;COOOCCH½CH3)? A. CH;COCI+ CH;CH2COO`Na* → B. CH;COOH +heat → C. CH3CH2CH2COCI + CH;COO Na* → D. A and CExplain how this occurred under mildly acidic conditions with a full mechanism.
- Propose a product and an arrow-pushing mechanism for the following reactions.X WP Question 20 of 26 - Module 3 V X dex.html?launchld-3ae80116-ce06-46c5-8cf0-5a4fefbe718f#/question/19 Question 20 of 26 (b) Incorrect. Propose an efficient synthesis for the following transformation: on DCL 1) A H 2) H₂O* E The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. TSCI, pyridine 1 PCC or DMP F NaOEt C Home - Learn with Chegg Ph3P=CH₂ + AICI 3 J 1) 2) H3O+ t-BUOK C G K Na2Cr₂O7, H2SO4, H₂O Mg D H conc. H₂SO4, heat L SAMSUNG OSO4, cat. NMO 0/1HW9 #5