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17. Draw the follow Draw the following line structure for the compound: 3,4,5-trimethyl-2,4-diheptendioic acid 18. Draw...
4. Draw the line-angle structure for each of the following a) (2E,4Z)-4-ethyl-5-isopropyl-3,6-dimethylocta-2,4-diene b) (2Z,4Z,6E)-3-bromo-5-chloro-4-ethyl-7-fluoro-9-methyldeca-2,4,6-triene c) (5S,8S)-3-sec-butyl-5-ethyl-1,8-dimethylcycloocta-1,3,6-triene d) 2-ethyl-3,5,5-trimethylcyclopenta-1,3-diene
____ 1. The diagram below represents serine, a polar, uncharged amino acid. Which functional group gives serine its distinct property? a. H3 b. CH2OH c. –H d. COO– ____ 2. The monomers shown below are monomers for which of the following natural polymers? a. polysaccharides b. plastics c. DNA d. proteins ____ 3. Which of the following processes illustrates the production of a protein? a. specific code for amino acids --> amino acid chain --> gene --> DNA --> specific...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines b. N.Methylpropanamine c. N.N-Diethylpentanamine 15.37 Briefly explain why the lower molar massamines (lewer than five carbons) exhibit appreciable solubility in water 15.38 Why is the salt of an amine appreciably more soluble in water than the mine from which it was formed 15.39 Most drugs containing amine groups are not administered as the mine but rather the amount you suggeste son why? 15.40 Why...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded in different orders. These may be further distinguished as chain isomers, which differ only in hydrocarbon chain structure, positional isomers, which differ in the location of a functional group, and functional group isomers which differ in the nature of their functional groups. Typically chain and position isomers show only modest differences in their physical and chemical properties, while functional group isomers differ greatly from...