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- Which of the following produces only butanoic acid (CH3CH2CH2 CO2H) being 'hydrolyzed in acid medium?Following are the steps in the industrial synthesis of glycerin. Provide structures for all intermediate compounds (AD) and describe the type of mechanism by which each is formed.Draw the organic product(s) of the reaction of phenylacetaldehyde with KMnO4. H3O+
- dedcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.Describe the trends in the acidityand physical properties of carboxylicacids, and explain how their acidityvaries with their substituents.For the generic ester RC(O)OR′, which bond will hydrolyzeunder basic conditions?(a) the R¬C bond (b) the C“O bond (c) the C¬O bond(d) the O¬R′ bond (e) more than one of the above
- Which of these reagent(s) will not react with HOCH2CH2CH2COOH? A) NaCN in ethanol B) C2H5OH in the presence of an acid catalyst. C) (CH3CO)2O D) Concentrated H2SO4Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With some reagents, no reaction occurs. CH3NH2, DCCReduction of an alkyl azide results in the formation of —-. A. an imine B. an oxime C. a tertiary amine D. a secondary amine E. a primary amine
- When a carboxylic acid is dissolved in isotopically labeled water, the label rapidly becomes incorporated into both oxygen atoms of the carboxylic acid. Explain.Melamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.IV. In every chemical reaction, include the IUPAC name and draw the structure of ALL organiccompounds present.A. Give the reacton on how to convert the following organic compounds. 1. N-Phenylpropionamide to alcohol 2. N-ethylbutylamide to alcohol