2. Draw a tetrahedral representation of the following compounds; a) R-2-chlorobutane c) S-2-butanol b) R-2-pentanol d)...
(R)-2-butanol Tetrahedral Fischer (H vert.) Fischer (H horz.) Skeletal (S)-2-chlorobutane Tetrahedral Fischer (H vert.) Fischer (H horz.) Skeletal Methamphetamine d-methamphetamine - methamphetamine Top attack Sec-butyl Cation Addition Reaction Products Bottom attack Assign (R or S to chiral carbons) COOH Нонн H- OH H- OH CH OH IH
Give the IUPAC name for the following compounds. 3, 3 diethyl dimethyl ethyl methyl butanol pentanol hexanol
Oxygen-containing Compounds 1. Which of the following will NOT convert 1-butanol into 1-chlorobutane in one step? a. SOCI2 b. PCl3 c. HCI d. CCl4
2. Signature (8 p.) Draw the appropriate structure for each of the following compounds a) (S)-3-allylcyclobutene b) (R)-1.1.3-triiodocycloheptane c) 1,7,7-tribenzylbicyclo[2.2.1 heptane d) meso-4.7-decanediol 3. (9 pts.) Name the following compounds in an unambiguous manner (use an accepted common or L.U.P.A.C. me): Me-16-H Mets Mesh Ao T-methyl-4-phenyl bicyclo [2.2.0/nexane (R)-2-methyl-3-pentanol
Determine the number of carbon and hydrogen types in the following molecules: 1. 3-Pentanol 2. 1-Butanol 3. 2-Pentanol 4. 2,3-Dimethyl-2-butanol 5. 3-Methyl-3-pentanol
Draw all the stereoisomers (redraw the first with the proper 3-D
representation) of the compounds below. The configuration for the
first isomer you should draw is provided. Assign R or S
configuration to each chirality center in the additional isomers.
Indicate the stereochemical relationship (diastereomers,
enantiomers, meso compounds) between the first isomer and each of
the others. The configuration for the Fischer Projection has been
omitted, since stereochemistry can be determined from a 2-D
structure. You do not need to...
30) Which of the following compounds is (are) symmetrical ethers? B)Only D) Only I, IIl, and IV A) Only III and IV C) Only I 31) What is the IUPAC of the following compound? но B) 1,1,4-Trimethyl-2-cyclohexanol D) 3,3,6-Trimethylcyclohexanol A) 2,5,5-Trimethylcyclohexanol ) 1,4,4-Trimethyl-2-cyclohexanol 32) What is the IUPAC of the following compound? он A) (R)-2,2-Dimethyl-3-pentanol C) (S)-2,2-Dimethyl-3-pentanol B) (S)-1-tert-Butyl-1-propanol D) (R)-4,4-Dimethyl-3-pentanol 33) What is the common name of the following compound? A) Methyl sec-butyl ether C) Isobutyl methyl ether B)...
1) Draw line-angle structures for these compounds. a. cis-2-pentene b. 1-butanol c. butanone 2) Identify the strongest IMF for each of the above compounds. a. ____________________ b. __________________ c. ________________________ 3) Draw at least 2 molecules of these compounds showing the IMFs that form between them. a. Cis-2-pentene (draw 2 or more molecules) b. 1-butanol (draw 2 or more molecules) 4) Which of the three compounds in question 1 is the most soluble in water? Give a brief explanation and...
Draw the structure of each compound
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (0) (s)-2-Methyl-1-butanol 2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol. 5. Identify...
24. Which of the following compounds cannot form hydrogen bonds between its molecules? A) CH3CH2CH2NHCH3 C) CH3CH2CH2CH2NH2 B) CH3CH2CH2OCH3 D) CH3CH2CH2CH2OH 25. What is the IUPAC of the following compound? (Draw the structure) (CH3CH2)3COH A) 2-Ethyl-2-pentanol 3-Ethyl-3-pentanol B) 2-Ethyl-3-pentanol 2,2-Diethyl-1-butanol COH DH