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- Give the products formed when benzaldehyde and benzoic acid are treated with the given reagents. a. Tollen’s reagentb. phenylhydrazine, H+c. HCNd. NH2OHe. 1 mole H2, Nif. 1 mole CH3OH, H+g. LiAlH4 then H2O, H+h. 2 moles CH3OH, H+i. CH3MgCl, then H2O, H+j. H2ODraw structural formulas for organic products A and B in the window below. Mg H20 A H3CC=CH2 ether Br • Draw only products having the organic portion of the original alkyl halide. • Draw carbon-lithium bonds using the single bond tool. If a structure has a copper-lithium bond, do not draw the lithium. • Separate products from different steps using the → sign from the drop-down menu.4- Choose the correct reactants required to synthesize the following molecule. H3CO OCH 3 A. Acetone and methanal B. Acetone and methanol C. Formaldehyde and propanal D. Formaldehyde and propanol 5- What is the IUPAC name of the following compound? CI A. 6-Chloro-4-ethoxy-1-octanal B. 6-Chloro-4-ethoxyoctanal C. 6-Chloro-4-ethoxycyclooctanal D. 4-Ethoxy-6-chlorooctanal - What is the IUPAC name of the following compound? 0 Br. Br Cl A. 2,6-Dibromo-3-chloro-5,5-dimethylhexanone B. 2,6-Dibromo-3-chloro-5,5-dimethylcyclohexanone C. 2,6-Dibromo-5-chloro-3,3-dimethylhexanone D. 2,6-Dibromo-5-chloro-3,3-dimethylcyclohexanone
- Table 1. Physical Properties of Selected Compounds Density (g/mL) Melting point (°C) Boiling point (°C) Substance Acetanilide 1.22 114 304 Acetone 0.79 -95 56 Benzophenone Bromoform 1.15 48 306 150 2.89 0.98 0.79 2.46 8 -2.4 2,3-Butanedione t-Butyl alcohol Cadmium nitrate 4H;O Chloroform Cyclohexane p-Dibromobenzene p-Dichlorobenzene Diphenyl Diphenylamine Diphenylnethane Ether, ethyl propyl 88 83 25 59 132 1.49 0.78 1.83 -63.5 6.5 86.9 61 81.4 219 1.46 53 70 53 27 174 0.99 255 1.16 302 265 1.00 1.37 -79 64 Hexane 0.66 69 Isopropyl alcohol Lauric acid 0.79 0.88 1.63 -98 83 225 330 43 Magnesium nitrate 6H2O Methyl alcohol Methylene chloride Naphthalene a-Naphthol Phenyl benzoate Propionaldehyde Sodium acetate 3H2O Stearic acid Thymol Toluene p-Toluidine Zinc chloride 89 79 1.34 -98 -97 65 40.1 1.15 1.10 80 218 94 288 1.23 71 314 0.81 1.45 0.85 0.97 -81 58 48.8 123 70 291 232 52 0.87 0.97 2.91 -95 111 45 200 283 732 MAR ...4. Start with NH3 and show step-by-step how the compound N-sec-butyl-N-isopropyl-3-pentanamine can be formed. Draw and name the reactants and products in each reaction (3 separate reactions.) 5. Salicylic acid (shown below) is a polyfunctional molecule (contains more than one functional group.) Circle and identify the functional groups on salicylic acid. Salicylic acid can react with ethanoic acid (acetic acid) to form aspirin. It can also react with ethanol to form ethyl salicylate, a compound with a minty smell used in perfume and artificial flavors. Draw out structures to illustrate each of these reactions. Discuss how these two reactions are similar and how they are different. HO, HODraw structural formulas for organic products A and B in the window below. CH3 CH3CCH₂CI _ CH3 Mg ether A A CH3OH B • Draw only products having the organic portion of the original alkyl halide. • Draw carbon-lithium bonds using the single bond tool. If a structure has a copper-lithium bond, do not draw the lithium. Separate products from different steps using the 1 sign from the drop-down menu.
- What feature of acetonitrile makes it a good solvent? Select one: A readily available lone pair of electrons b. An acetate group c. A carbon-nitrogen triple bond d. Its ability to chelate a metal atomRemaining Time: 1 hour, 23 minutes, 09 seconds. ✓ Question Completion Status: OE. Ether QUESTION 4 The functional group contained in the compound O A. thiol B. carboxylic acid OC. amine O D. ester O E. amide QUESTION 5 0 II CH3-CH2-C-O-CH 3 What is (are) the product(s) of the complete combustion of any hydrocarbon? is a(n)Draw the structure(s) of the major organic product(s) of the following reaction. H. 1. KMno, / NaOH 2. aqueous HCI • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple products using the + sign from the drop-down menu.
- The molecule below is reacted with ethylene glycol in acidic conditions. The product contains the following functional groups. u. a. An ester and an acetal b. An acetal and a hemiacetal c. A hemiacetal and a carboxylic acid d. Two different acetals + 4 HO OHWhat reaction will occur when benzoic acid is mixed with sodium bicarbonate? (Hint: benzoic acid is an acid and sodium bicarbonate is a base...) What three products will be generated by this reaction? (You may have to look this one up...) HO. Na HO.1l Normal l No Spac. A-空,A. KJIDPAL U - abx X, Paragraph Font Easter makes unique smells: 2-methyl-2-butanol + acetic acid →> 3-methyl-2-butanol + acetic acid –> 1-propanol + acetic acid –> 1-Octanol + acetic acid -> 2-methyl - propanol + formic acid acetic acid –> LA English (United States) to search