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Q: Question attached
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How many asymmetrical carbon/s is/are present in the given structure?
CH3CHBrCH2CHClCH3CH3CHBrCH2CHClCH3
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- Indicate whether the pair of structures shown represent stereoisomers, constitutional isomers, different conformations of the same compound, or the same conformation of a compound viewed from a different perspective. Note that cis, trans isomers are an example of stereoisomers. CH3 CH3 CI CI H H H. H CH3 H. H' H. CH3 Submit Answer Retry Entire Group 6 more group attempts remaining (Previous Next Save and Exit Cengage Learning | Cengage Technical Support MacBook Air DII 888 F12 F10 F7 F4 & 9 delete - 4 5 6 8 { т Y U P F G J K 1r command eption .. ..Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Br HI!... OH Molecule 1 *** H" Br H Molecule 4 OH Br OH Onone of the above Molecule 2 H Br Br ""OH ОН Molecule 5 OH _ H Molecule 3 Br CI H Molecule 6 Br H OH X 5How many asymmetric centers are present in a molecule of 2,4,6-trimethylheptane? please answer me
- 6. For each pair of compounds below determine whether they represent the same molecule, enantiomers, or diastereomers. CH H₂N H CH J OllinO 2||2 COOH C OH CH₂ OH NH₂ CH, COOH CH3 HO H₂N CH₂4 CH CCC COOH OH NH₂ NIIIIIC CH₂ H CH3 CH3 H₂N HO H₂N COOH CH OH 5- O J CH3 COOH O H CH₂ H COOH HO CH CH₂4 HOOC COOH ........ OH JCC H NH₂ NH₂ CH₂Label each of the following as cis, trans or neither. Below each structure that is cis draw a transconfigurational stereoisomer or vice versa.Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
- Remaining Time: 40 minutes, 37 seconds. Question Completion Status: Moving to another question will save this response. Question 23 esc How many tetrahedral stereocenters are present in this compound? OH CH3CH₂CHCHCHCH₂CH3 CH3 CH₂CH3 A Moving to another question will save this response. O F2 20 F3 000 F4 MaQuestion: Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Molecule 1 Molecule 2 Molecule 3 NH Molecule 4 Molecule 5 Molecule 6 HN NH. HN O none of the above Reply..28) Label each asymmetric carbon in the molecule below as having the R or S configuration. HO2C F H3CH2CH3
- Compound 1 Br Bri НІ T ... H The correct IUPAC names are: Compound 2 H Br Br I.. H Br The compounds are diastereomers not isomeric enantiomers identical constitutional isomers Compound 1: (2R, 3R)-1,2,3-tribromobutane, Compound 2: (2S, 3R)-1,2,3-tribromobutane Compound 1: (2R, 3S)-1,2,3-tribromobutane, O Compound 1: (2R,3R)-1,2,3-tribromobutane, Compound 2: (2S,3S)-1,2,3-tribromobutane Compound 2: (2R, 3R)-1,2,3-tribromobutane O Compound 1: (2S,3S)-1,2,3-tribromobutane, Compound 2: (2R,3S)-1,2,3-tribromobutaneFor each organic compound in the table below, enter the locant of the highlighted side chain. CH3- CH3- — CH3- — CH3 1 CH₂ | C | CH₂ - CH3 1 CH, 1 — | CH₂ CH3 1 CH₂ - CH₂ compound CH₂- CH₂ - — CH₂- CH3 CH- CH₂ | CH CH, | CH - CH 1 CH3 CH-CH3 CH₂ | CH3 CH3 — CH₂ CH3 locant of highlighted side chain 0a) Identify the hydrogens on the prochiral carbon atom(s) in the following molecules as pro-R or pro-S. HO H₂C OCH3 H b) H3C H HO CH3 ""|| H