Identify the functional groups in each molecule. Classify each alcohol, alkyl halide, amide, and amine as 1°, 2°, or 3º. H. a. с. Но- е. ibuprofen (analgesic) Но penicillin G (an antibiotic) Darvon (analgesic) H2N. b. d. OH pregabalin trade name Lyrica (used in treating chronic pain) pyrethrin I (potent insecticide from chrysanthemums) histrionicotoxin (poison secreted by a
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- Below is a primary alcohol or and an aldehyde (of same carbon length). Which is more likely to be soluble in water?Identify and label all functional groups of Carvone (alcohols, amines, amides, carboxylic acids, ketones, aldehydes, aromatic rings, aromatic amines, etc) on the Lewis Structure. You do not have to circle alkanes.i. Why is the boiling point of the aldehyde greater than that of the alkane? ii. Why is the boiling point of alcohol the highest? iii. Explain why the solubility of aldehydes and alcohols falls as the molecules get bigger.
- Please write the answer clearly with the state of matter following each compound.(a) Identify the functional groups in salinosporamide A, an anticanceragent isolated from marine sediment. (b) Classify each alcohol, alkylhalide, amide, and amine as 1°, 2°, or 3°.The structure of Tamiflu, an anti-influenza drug, is shown below (Organic Lett. 2007, 259). Circle and identify each functional group in Tamiflu.
- Linolenic acid (Table 10.2) and stearidonic acid are omega-3 fatty acids, unsaturated fatty acids that contain the first double bond located at C3, when numbering begins at the methyl end of the chain. Predict how the melting point of stearidonic acid compares with the melting points of linolenic and stearic acids. A current avenue of research is examining the use of soybean oil enriched in stearidonic acid as a healthier alternative to vegetable oils that contain fewer degrees of unsaturation.only write their functional group. no explanation neededShow the stepwise mechanism. Show all lone pairs and formal charges
- based on the lews dot structure for each solvent rate the relative polarity of each solvent. (List them from least polar to most polar) Solvents: hexane, isopropyl alcohol, methanol, saltineIdentify and label all functional groups (alcohols, amines, amides, carboxylic acids, ketones, aldehydes, aromatic rings, aromatic amines, etc) of Carvone on the Lewis Structure. You do not have to circle alkanes. Make sure to add additional details about the functional groups of Carvone1. Answer the following question using the case study if needed (images included) in detail: a) In the Chapter 8 case study, Charles Cullen administered many drugs to his victims, including the cardiac medicine Digitalis. The main active compound in digitalis is digoxin. Look up the structure of digoxin either online or in the textbook (be sure to cite your source), and identify any three functional groups in the chemical structure of digoxin. Indicate the number of rings (cyclic structures) present in the molecule as well.