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7. What is the configuration of the following compound? СН3 H-1-ci Cl-- CH2CH3 A)...
29 Give the configurations, respectively, of the following two molecules. CH HO H and CI A. B. C....
29 Give the configurations, respectively, of the following two molecules. CH HO H and CI A. B. C. R and R R and S S and S D. S and R 30 Give the configurations, reypectively, of the folowing two molecules H CH CHy A. B. C. R and R R and S Sand S D. S and R Which one of the following groups has the highest rank as assigned by the Cahn- Ingold-Prelog system for stereogenic (chiral) carbons?...
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...
thanm yoy!!! OH I r I LOH 24. What is the correct stereochemical designation for compound...
thanm yoy!!!
OH I r I LOH 24. What is the correct stereochemical designation for compound T? d. 2S, 3S, 4R e.. 2R, 3R, 4R d. - a. 2S, 3R, 4R b. 2R, 3R, 45 c. 2S, 3S, 4S R 4R 25. What is the correct stereochemical designation for compound I? a. 2R, 3S, 4S b. 2S, 3S,4R c. 2R, 3R, 4R d. 2S, 3R, 4R e. 2S, 3S, 4S
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...
Is my naming correct? CH3З CH3 Br .CH2CH3 (b) (a) НО CH2Br Н H Н (S)-1-bromo-2-propanal...
Is my naming correct?
CH3З CH3 Br .CH2CH3 (b) (a) НО CH2Br Н H Н (S)-1-bromo-2-propanal 3-bromopentane Br CH3 (d) (c) HIIl" H OH H OH CI CH3 (2S,3S)-2-bromo-3-chlorobutane (2S,3R)-2,3-butanediol / meso compound
explanations too pls! Will rate only if answers are complete What R and/or S configuration notation...
explanations too pls!
Will rate only if answers are complete
What R and/or S configuration notation would be used for this structure? A) 2R, 3R B) 2S, 3R C) 2R, 3S D) 2S, 3S Which of the following is not an acyl derivative of a carboxylic acid? A) nitrile B) amide C) ester D) acid chloride Which of the following is not a common feature of both carboxylic acids and nitriles? A) Carbon atom with three bonds to an electronegative...
Which of the following structures is most stable? 2) How many stereoisomers does the molecule below...
Which of the following structures is most stable? 2) How many stereoisomers does the molecule below have? (СН), С+ снен снаси сна OH CH₃ br. a) 3 6) 4 c) 6 d) 8 e 9 3) Which of the following molecules below are chiral? 0) to A Boh A MOH HOS DBr e) 1, 2 and 3 a) Only 1 b) 1 and 3 c) 2 and 3 d) 1 and 3 What is the relationship between the following two...
need help on the last hw problems please explain and answer 43. An unknown compound of...
need help on the last hw problems please explain and
answer
43. An unknown compound of formula CeH16 was found to be optically active. On catalytic reduction of the unknown compound over a palladium catalyst, 2 equivalents of hydrogen were absorbed. Ozonolysis of the unknown compound gave two products: one was identified as an optically active dialdehyde of formula CsHaO2; the other compound was identified as acetaldehyde (CH3CHO). The most likely structure of the unknown compound is B. CH.CH-CH-CHECH CH...
age 7 19. The reaction of CH, CH, CCH, CH, with H,/Ni forms a. pentane. b....
age 7 19. The reaction of CH, CH, CCH, CH, with H,/Ni forms a. pentane. b. one particular chiral pentanol. c. an equimolecular mixture of two chiral pentanols . d. one achiral pentanol. e. no product. 20. The p-orbital of a methyl radical carbon, CH,, Contains how many electrons? a. 1 b. 2 e. 3 d. 4 e. 0 21. (2R, 35)-2,3-Dichlorobutane and (25, 3R) -2,3-dichlorobutane are: a. enantiomers b. diastereomers e. identical d. conformational isomers e. constitutional isomers 22....
A. aldehyde B. ketones C. carboxylic acids D. esters 7, How many stereoisomers of 2,4-pentanediol are...
A. aldehyde B. ketones C. carboxylic acids D. esters 7, How many stereoisomers of 2,4-pentanediol are possible? но он В. З A. 2 C. 4 D. 6 8.Which one of the following is a diastereomer of (2R, 3R)-2,3-dibromopentane? A. (2S,3S)-2,3-dibromopentane C.R-1,2-dibromopentane B. (2S,3R)-2,3-dibromopentane D. (2R,4R)-2,4-dibromopentane 9. Which one of the following groups has the highest rank as assigned by the Cahn-Ir Prelog system for stereogenic carbons? A. -CH-CH2 B. -CH20H C.-CH-0 D. -CH2SH 10. Which of the following statements are...
29 Give the configurations, respectively, of the following two molecules. CH HO H and CI A. B. C. R and R R and S S and S D. S and R 30 Give the configurations, reypectively, of the folowing two molecules H CH CHy A. B. C. R and R R and S Sand S D. S and R Which one of the following groups has the highest rank as assigned by the Cahn- Ingold-Prelog system for stereogenic (chiral) carbons?...
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...
thanm yoy!!!
OH I r I LOH 24. What is the correct stereochemical designation for compound T? d. 2S, 3S, 4R e.. 2R, 3R, 4R d. - a. 2S, 3R, 4R b. 2R, 3R, 45 c. 2S, 3S, 4S R 4R 25. What is the correct stereochemical designation for compound I? a. 2R, 3S, 4S b. 2S, 3S,4R c. 2R, 3R, 4R d. 2S, 3R, 4R e. 2S, 3S, 4S
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...
Is my naming correct?
CH3З CH3 Br .CH2CH3 (b) (a) НО CH2Br Н H Н (S)-1-bromo-2-propanal 3-bromopentane Br CH3 (d) (c) HIIl" H OH H OH CI CH3 (2S,3S)-2-bromo-3-chlorobutane (2S,3R)-2,3-butanediol / meso compound
explanations too pls!
Will rate only if answers are complete
What R and/or S configuration notation would be used for this structure? A) 2R, 3R B) 2S, 3R C) 2R, 3S D) 2S, 3S Which of the following is not an acyl derivative of a carboxylic acid? A) nitrile B) amide C) ester D) acid chloride Which of the following is not a common feature of both carboxylic acids and nitriles? A) Carbon atom with three bonds to an electronegative...
Which of the following structures is most stable? 2) How many stereoisomers does the molecule below have? (СН), С+ снен снаси сна OH CH₃ br. a) 3 6) 4 c) 6 d) 8 e 9 3) Which of the following molecules below are chiral? 0) to A Boh A MOH HOS DBr e) 1, 2 and 3 a) Only 1 b) 1 and 3 c) 2 and 3 d) 1 and 3 What is the relationship between the following two...
need help on the last hw problems please explain and
answer
43. An unknown compound of formula CeH16 was found to be optically active. On catalytic reduction of the unknown compound over a palladium catalyst, 2 equivalents of hydrogen were absorbed. Ozonolysis of the unknown compound gave two products: one was identified as an optically active dialdehyde of formula CsHaO2; the other compound was identified as acetaldehyde (CH3CHO). The most likely structure of the unknown compound is B. CH.CH-CH-CHECH CH...
age 7 19. The reaction of CH, CH, CCH, CH, with H,/Ni forms a. pentane. b. one particular chiral pentanol. c. an equimolecular mixture of two chiral pentanols . d. one achiral pentanol. e. no product. 20. The p-orbital of a methyl radical carbon, CH,, Contains how many electrons? a. 1 b. 2 e. 3 d. 4 e. 0 21. (2R, 35)-2,3-Dichlorobutane and (25, 3R) -2,3-dichlorobutane are: a. enantiomers b. diastereomers e. identical d. conformational isomers e. constitutional isomers 22....
A. aldehyde B. ketones C. carboxylic acids D. esters 7, How many stereoisomers of 2,4-pentanediol are possible? но он В. З A. 2 C. 4 D. 6 8.Which one of the following is a diastereomer of (2R, 3R)-2,3-dibromopentane? A. (2S,3S)-2,3-dibromopentane C.R-1,2-dibromopentane B. (2S,3R)-2,3-dibromopentane D. (2R,4R)-2,4-dibromopentane 9. Which one of the following groups has the highest rank as assigned by the Cahn-Ir Prelog system for stereogenic carbons? A. -CH-CH2 B. -CH20H C.-CH-0 D. -CH2SH 10. Which of the following statements are...
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