Ph 4. (2 points) Circle the correct name of the following structure. a) (meso)-hydrobenzoin HOH b) (1R, 2R)-hydrobe...
1. (2 points each) Draw the chemical structures of the following two compounds. iodoform 71-butanal 2. (2 points) Circle the compound that will give a positive result in the iodoform test. (a) acetophenone b) cyclopentanone c) isobutanol d) n-heptanal 3. (3 points) Convert the following molecule to a Fisher projection. OH | H Convert to a Fisher Projection H DH 1 OHHH HAH HEBH 4. (2 points) Circle the correct name of the following structure. ph a) (meso)-hydrobenzoin H -OH...
What is the correct IUPAC name of the following compound? (1S,2R)-1-iodo-2-methylcyclohexane (1S,2S)-1-iodo-2-methylcyclohexane (1R,2R)-1-iodo-2-methylcyclohexane (1R,2S)-1-iodo-2-methylcyclohexane Which group has the highest priority in the Cahn-Ingold-Prelog priority system? Give the highest ranking group a priority of 1 and the lowest ranking group a priority of 4. --CO2H-CONH2 Rank the following groups in terms of their priority according to the Cahn-Ingold-Prelog system of prioritles. Give the highest ranking group a priority of 1 and the lowest ranking group a priority of 4
CO5T0306483 What is the correct IUPAC name of the following compound? (15,2R)-1-ethyl-2-methylcyclohexane (1R, 2S)-1-ethyl-2-methylcyclohexane (1R 2R)-1-ethyl-2-methylcyclohexane (15,2S)-1-ethyl-2-methylcyclohexane
4) Draw the following compounds a. (2S,5R)-5-chloro-2-ethylhexanoic acid b. (1R,2R,4R)-4-ethylcyclohexane-1,2-diol c. (2S,3R)-3-amino-2-phenylbutanal d. (1S,2S,3R)-2-fluoro-3-propylcyclobutanol e. (2E, 7Z)-5-bromo-2,7-nonadiene
26. Choose the correct R/S designations for the indicated stereocenters. Meo Explain N Ph A 1R 2R D 15,2R (в 19,25 Not Stereocenters 1R.25 C 27. Choose the pair of representations that both represent the same meso compound. NH2 HAN NH2 NH2 NH2 H NH NH2 NH2 Et B NH2 NH2 NH2 NH2 HN NH NH2 NH2 E!
c. cis-1-metbylbicylol0.4.4ldecan 24. Which structure is syn? d. trans-1-methylbicyclo[0.4.41derane e. not a.-d с. e. not a.-d 25. Monocyclic alkenes (for example, cyclepropene, cyclobutene, etc.) up to 7 carbons are all? a. b. R C. S d. Z e. not a.-d. 26. The following stereoisomer of a controlled substance is? (Hint: The alcohol is the 1 carbon.) a. 1R, 2R) b. (1R, 25) c. (1S, 2R) d. (1S, 2S) e. not a.-d 27. The carbon with the asterisk is? a. с....
Which is the correct name for the compound shown below? H. O (2R,35)-2-Bromo-3-chlorobutane (25,3R)-2-Bromo-3-chlorobutane (2R, 3R)-2-Bromo-3-chlorobutane (2S,3S)-2-Bromo-3-chlorobutane Which compound is achiral? O meso-2,5-Difluorohexane O trans-1,2-Dimethylcyclohexane O (S)-3-lodohexane (2R, 3R)-2,3-Dibromoheptane 1
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve active opti call active 8. (3 pts) How many stereoisomers are there of 2,3-dibromobutane? 4 sleeoisamvers (8 pts) Circle the letter of the statements that are true. a. Racemic mixtures are optically active Enantiomers have specific rotations that are equal, but have opposite signs 9. o adtc) Achiral molecules are optically inactive d Meso compounds contain equal amounts of enantiomers 4pts) Complete the Fischer...
12 The IUPAC name for the following compound is (circle your choice): (i)(2S, 3S)-2,3-dibromopentane (ii) (2R, 3R)-2,3-dibromopentane CH (iii) (2R, 3S)-2,3-dibromopentane Br - H (iv)(2S, 3S)-2,3-dibromobutane H + Br 13 CH.CH Provide IUPAC names for the followmg compounds. Include trans or cis, E or Z to stereochemistry.
Draw a dash-wedge structure for the following? (a) (1R)-1-bromo-1,3,3trimethylcyclohexane (b) (2S, 4S)- 2-bromo-4-methylhexane provide r and s please