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OH I r I LOH 24. What is the correct stereochemical designation for compound...
Use the pair of compounds below to answer the next three questions: OH Br TBr LOH...
Use the pair of compounds below to answer the next three questions: OH Br TBr LOH 24. What is the correct stereochemical designation for compound IT? a. b. c. 2S, 3R, 4R 2R, 3R, 4S 2S, 3S, 45 d. 2S, 3S,4R e. 2R 3R 4R 25. What is the correct stereochemical designation for compound I? a. 2R, 3S, 4S b. 2S, 3S,4R c. 2R, 3R, 4R d. 28, 3R, 4R e. 2S, 3S,4S 26. What term best describes the structural...
What is the correct R/S configuration for each of the three stereocenters in the molecule below...
What is the correct R/S configuration for each of the three
stereocenters in the molecule below
Choose the best term that best describes the relationship
between this pair of molecules
1) What is the correct R/S configuration for each of the three stereocenters in the molecule below (1 mark) CH3 -ОН Н- -ОН Н- -OH Н- CH2CH3 a) 2R, 3S, 4R b) 2R, 3R, 4S c) 2S, 3R, 4R d) 2S, 3S, 4R е) 28, 3R, 4S 2) Choose the...
Indicate the stereochemical configuration for the tetrahedral centers shown below. OR OS not a configuration center...
Indicate the stereochemical configuration for the tetrahedral centers shown below. OR OS not a configuration center Br R OS not a configuration center ООО Select the proper IUPAC name for the following compound, including the (R) or (S) designation where appropriate. Н. - (2R,3S)-2-chloro-3-methylpentane (29,3R)-2-chloro-3-methylpentane (2R 3R)-2-chloro-3-methylpentane O (2S,3S)-2-chloro-3-methylpentane Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for...
Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not...
Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound 1: (3R.4S)-3,4-dimethylheptane, Compound II: (3S,4R)-3,4-dimethylheptane Compound I: (3S,4S)-3,4-dimethylheptane, Compound II: (3S,4S)-3,4-dimethylheptane Compound I: (3R.4S)-3,4-dimethylheptane, Compound II: (3S,4S)-3,4-dimethylheptane Compound 1: (3S,4S)-3,4-dimethylheptane, Compound II: (3R.4S)-3,4-dimethylheptane
12) What is the IUPAC name of the compound shown below? C₂H, Br- CH3 H-I-C1 CH3...
12) What is the IUPAC name of the compound shown below? C₂H, Br- CH3 H-I-C1 CH3 (A)(2R,3S,4S)-2-chloro-3,4-dibromo-3-methylhexane BX2R,3S,4S)-3,4-dibromo-2-chloro-3-methylhexane C) (3S,4S,5S)-3,4-dibromo-5-chloro-4-methylhexane D) (2R,3R,4S)-3,4-dibromo-2-chloro-3-methylhexane E) (2R,3S,4R)-3,4-dibromo-2-chloro-3-methylhexane
Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not...
Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound I: (2S, 3S)-1, 2, 3-tribromobutane, Compound II: (2R, 3S)-1, 2, 3-tribromobutane Compound I: (2R, 3S)-1, 2, 3-tribromobutane, Compound II: (2S, 3S)-1, 2, 3-tribromobutane Compound I: (2R.3RH, 2, 3-tribromobutane, Compound II: (2S, 3R)-1, 2, 3-tribromobutane...
The following common sweetener and dog poison is? (2R, 4R) (2S, 4S) (2R, 3s, 4S) (2R,...
The following common sweetener and dog poison is? (2R, 4R) (2S, 4S) (2R, 3s, 4S) (2R, 3r, 4S] not The following c/s-3(8-dimethylbicyclo[3.2.l]octane is? exo, anti exo, syn endo, anti endo, syri e. not a.-d. The following compound is? E Z both a. and b. not a.-c.
12) What is the IUPAC name of the compound shown below? C2HS Br CH 3 Br...
12) What is the IUPAC name of the compound shown below? C2HS Br CH 3 Br C1 Н CH 3 A) 2R,3S,4S)-2-chloro-3,4-dibromo-3-methylhexane B 2R,3S,4S)-3,4-dibromo-2-ch loro-3 -methylhexane C) (3S,4S,5S)-3,4-dibromo-5 -chloro-4-methylhexane D) (2R,3R,4S)-3,4-dibromo-2-chloro-3-methylhexane E) (2R,3S,4R)-3,4-dibromo-2-chloro-3-methylhexane H
a. Assign the correct stereochemical descriptors to every stereocenter in the molecule below SH HN b....
a. Assign the correct stereochemical descriptors to every stereocenter in the molecule below SH HN b. A Fischer projection for a polyhydroxy diacid is shown below. 1. Draw a bond-line projection for this molecule. 2. Draw the mirror image of the projection you drew above, then convert your mirror- image drawing into a Fischer projection. c. Shown below are Newman projections for (2R,3R)-, (2R,3S), and (2S,3S)-2,3-dichlorobutane. 1. Which is which? 2. Which compound is a meso compound?
please explain 7. What is the configuration of the following compound? СН3 H-1-ci Cl-- CH2CH3 A)...
please explain
7. What is the configuration of the following compound? СН3 H-1-ci Cl-- CH2CH3 A) 2S, 3R B) 3R, 3S C) 2S, 3S D) 2R, 3R E) Can't do R and S; the compound is achiral.
Use the pair of compounds below to answer the next three questions: OH Br TBr LOH 24. What is the correct stereochemical designation for compound IT? a. b. c. 2S, 3R, 4R 2R, 3R, 4S 2S, 3S, 45 d. 2S, 3S,4R e. 2R 3R 4R 25. What is the correct stereochemical designation for compound I? a. 2R, 3S, 4S b. 2S, 3S,4R c. 2R, 3R, 4R d. 28, 3R, 4R e. 2S, 3S,4S 26. What term best describes the structural...
What is the correct R/S configuration for each of the three
stereocenters in the molecule below
Choose the best term that best describes the relationship
between this pair of molecules
1) What is the correct R/S configuration for each of the three stereocenters in the molecule below (1 mark) CH3 -ОН Н- -ОН Н- -OH Н- CH2CH3 a) 2R, 3S, 4R b) 2R, 3R, 4S c) 2S, 3R, 4R d) 2S, 3S, 4R е) 28, 3R, 4S 2) Choose the...
Indicate the stereochemical configuration for the tetrahedral centers shown below. OR OS not a configuration center Br R OS not a configuration center ООО Select the proper IUPAC name for the following compound, including the (R) or (S) designation where appropriate. Н. - (2R,3S)-2-chloro-3-methylpentane (29,3R)-2-chloro-3-methylpentane (2R 3R)-2-chloro-3-methylpentane O (2S,3S)-2-chloro-3-methylpentane Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for...
Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound 1: (3R.4S)-3,4-dimethylheptane, Compound II: (3S,4R)-3,4-dimethylheptane Compound I: (3S,4S)-3,4-dimethylheptane, Compound II: (3S,4S)-3,4-dimethylheptane Compound I: (3R.4S)-3,4-dimethylheptane, Compound II: (3S,4S)-3,4-dimethylheptane Compound 1: (3S,4S)-3,4-dimethylheptane, Compound II: (3R.4S)-3,4-dimethylheptane
12) What is the IUPAC name of the compound shown below? C₂H, Br- CH3 H-I-C1 CH3 (A)(2R,3S,4S)-2-chloro-3,4-dibromo-3-methylhexane BX2R,3S,4S)-3,4-dibromo-2-chloro-3-methylhexane C) (3S,4S,5S)-3,4-dibromo-5-chloro-4-methylhexane D) (2R,3R,4S)-3,4-dibromo-2-chloro-3-methylhexane E) (2R,3S,4R)-3,4-dibromo-2-chloro-3-methylhexane
Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound I: (2S, 3S)-1, 2, 3-tribromobutane, Compound II: (2R, 3S)-1, 2, 3-tribromobutane Compound I: (2R, 3S)-1, 2, 3-tribromobutane, Compound II: (2S, 3S)-1, 2, 3-tribromobutane Compound I: (2R.3RH, 2, 3-tribromobutane, Compound II: (2S, 3R)-1, 2, 3-tribromobutane...
The following common sweetener and dog poison is? (2R, 4R) (2S, 4S) (2R, 3s, 4S) (2R, 3r, 4S] not The following c/s-3(8-dimethylbicyclo[3.2.l]octane is? exo, anti exo, syn endo, anti endo, syri e. not a.-d. The following compound is? E Z both a. and b. not a.-c.
12) What is the IUPAC name of the compound shown below? C2HS Br CH 3 Br C1 Н CH 3 A) 2R,3S,4S)-2-chloro-3,4-dibromo-3-methylhexane B 2R,3S,4S)-3,4-dibromo-2-ch loro-3 -methylhexane C) (3S,4S,5S)-3,4-dibromo-5 -chloro-4-methylhexane D) (2R,3R,4S)-3,4-dibromo-2-chloro-3-methylhexane E) (2R,3S,4R)-3,4-dibromo-2-chloro-3-methylhexane H
a. Assign the correct stereochemical descriptors to every stereocenter in the molecule below SH HN b. A Fischer projection for a polyhydroxy diacid is shown below. 1. Draw a bond-line projection for this molecule. 2. Draw the mirror image of the projection you drew above, then convert your mirror- image drawing into a Fischer projection. c. Shown below are Newman projections for (2R,3R)-, (2R,3S), and (2S,3S)-2,3-dichlorobutane. 1. Which is which? 2. Which compound is a meso compound?
please explain
7. What is the configuration of the following compound? СН3 H-1-ci Cl-- CH2CH3 A) 2S, 3R B) 3R, 3S C) 2S, 3S D) 2R, 3R E) Can't do R and S; the compound is achiral.
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