Problems and questions an administered to patient 1. Why we drugs that cawain the smile functional...
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...
1. What is the correct assignment of the names of the functional groups in the following nitrogen-containing compound? 2. What is the IUPAC name of the following compound. 3. Which of the following is the weakest base? 4. What is the hybridization of the nitrogen atom of pyridine 5. What is the major organic product obtained from the following reaction? Clcle he Best choice for each. 1. What is the correct assignment of the names of the functional groups in...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
____ 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...
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...