Homework Answers
(a) So, the absolute R and S
configuration with their IUPAC name of the given molecule including
their numbering of the group (on their priority basis) and the
direction of rotation is given as below:-
(b) So, the absolute R and S configuration with their IUPAC name of the given molecule including their numbering of the group (on their priority basis) and the direction of rotation is given as below:-
(c) So, the absolute R and S configuration with their IUPAC name of the given molecule including their numbering of the group (on their priority basis) and the direction of rotation is given as below:-
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6.6 Indicate whether the asymmetric atom in each of the following compounds has the R or...
Indicate whether the asymmetric atom in each of the following compounds has the R or S...
Indicate whether the asymmetric
atom in each of the following compounds has the R or S
configuration.
Indicate whether the asymmetric atom in each of the following compounds has the R or S configuration.
star each asymmetric carbon atom in the following examples & determine whether it has the R...
star each asymmetric carbon atom in the following examples
& determine whether it has the R or S configuration
PROBLEM 5-6 Star () each asymmetric carbon atom in the following examples, and determine whether it has the (R) or (S) configuration. сн, Н Н H CH, (c) H. (a) (b) Br но с, CH сH CH, CH,CH НС н н CH, Н (d) (e) (D Н Н Cl H Cl Cl СНO (g) (h) ("i) CH CH, (CH,O),CH CH(CH), D...
8. Indicate whether each of the following statements is true or false. If a statement is...
8. Indicate whether each of the following statements is true or false. If a statement is false, explain why a) Two structural isomers may be chiral. : True b) A compound must be chiral in order to have an enantiomer. True c) A chiral compound with an asymmetric carbon atom designated always has a positive optical rotation. False (R) as d) Mirror-image molecules are always enantiomers. False chiral. False e) All compounds with asymmetric carbon atoms are f)The relative configuration...
Which of the following chiral compounds is(are) R enantiomer(s)? 1) I. II III но, CI. Н,с...
Which of the following chiral compounds is(are) R enantiomer(s)? 1) I. II III но, CI. Н,с CH CI OH н,с 2) You found an organic compound containing chiral carbon atom with the following four substituents: HC C-, CI-, O C- and H2C-CH-, What would be the correct order of their priorities? A) HC C-> O-C->CI-> H2C-CH B) Cl->HCC-> 0-C-> H2C-CH C) Cl-> O C-> HC C-> H2C-CH D) Cl-> O-C-> H2C-CH-> HC C E) O-C-> Cl-> HC C-> H2C-CH 3)...
please explain your answers 11. Indicate whether the pairs of compoun whether the pairs of compounds...
please explain your answers
11. Indicate whether the pairs of compoun whether the pairs of compounds shown below are enantiomers, diastereomers, structural (constit. ructural constitutional) isomers, the same compound, or different compounds which are not isomers. (0.25 pts ea = 1 pt) Structural H OH Vs. constitutional но н OH CHE H OH vs. dia stereomers BE BroH. H₂CH₂CH CH3 HOCH2 CHO here the we dia stereomers distoremos он он носна сно н CNHO VS HOC 2 TNH₂ CH SH...
please go into detail (about S and R configuration) as im having difficulty with this. thanks...
please go into detail (about S and R configuration) as im having
difficulty with this.
thanks
achiral 5.58 Draw bond-line structures using wedges and dashes for the following compounds: 5. rel CHE НЕОН Нонн нон (а) Сн, Et Н -ОН НО-Ен нон (b) Me Et HO- H НЕОН Нон Me (а) (c) 5.6 Me me Н но (d) Me -СІ -н Me CI- НО (e) H -н Me 5.6. 5.59 The following questions apply to the five compounds in the...
7. How are these two compounds related to each other: same compound, structural isomers, enantiomers diastereomers?...
7. How are these two compounds related to each other: same compound, structural isomers, enantiomers diastereomers? сH, сн, Answer OH HO н- H он но -н Н- CH, CH, 8. How are these two compounds related to each other: same compound, structural isomers, enantiomers, diastereomers? сH,он CH,OH Answer: Но Н- Он н Н OH но- -н CH сH, 9. (R)-tartaric acid has a specific rotation of +12.0 degrees. a) What is the specific rotation of (S)-tartaric acid? b) What is...
5. (3 pts each) For the following pairs of molecules, indicate if they are identical different compounds. enantiomer...
5. (3 pts each) For the following pairs of molecules, indicate if they are identical different compounds. enantiomers, diastereomers, or constitutional isomers CHE CH H3COH and HOT но — сня нас — Br Hc- Br CH2OH Леон нон он and a нус он Он но- нс сня CI HOBO но and нстве
1. Use VSEPR theory to predict the molecular geometry for each of the following molecules, indicate...
1. Use VSEPR theory to predict the molecular geometry for each of the following molecules, indicate whether each bond in it is a a or m bond, and provide the hybridization scheme for each non-hydrogen atom а. Н.С %3 снCH %3D CH, b. (носн»),С(СH,)соон с. CH,соосH(CHә)сн — снс 3D ссн, e. (CH3),СHCH,CH(NH,)C0OH d. CH,онсH(NH,)соон 2. Write the resonance structures and resonance hybrid for each of the following ions. Use curved arrows to show the shifts in electrons. ь. CH3 d....
biochem 7. Indicate whether each of the following carbohydrates is reducing or nonreducing: HO GHOH он...
biochem
7. Indicate whether each of the following carbohydrates is reducing or nonreducing: HO GHOH он нонни У SH,OH cң он HỌ O OCH е ну о чно он НА но то он (c) HOCHZ0. ÇH,OH ну CH,OH а, ОЛОН 4 на Xно- ньон yoXч на ко, ОН Н
Indicate whether the asymmetric
atom in each of the following compounds has the R or S
configuration.
Indicate whether the asymmetric atom in each of the following compounds has the R or S configuration.
star each asymmetric carbon atom in the following examples
& determine whether it has the R or S configuration
PROBLEM 5-6 Star () each asymmetric carbon atom in the following examples, and determine whether it has the (R) or (S) configuration. сн, Н Н H CH, (c) H. (a) (b) Br но с, CH сH CH, CH,CH НС н н CH, Н (d) (e) (D Н Н Cl H Cl Cl СНO (g) (h) ("i) CH CH, (CH,O),CH CH(CH), D...
8. Indicate whether each of the following statements is true or false. If a statement is false, explain why a) Two structural isomers may be chiral. : True b) A compound must be chiral in order to have an enantiomer. True c) A chiral compound with an asymmetric carbon atom designated always has a positive optical rotation. False (R) as d) Mirror-image molecules are always enantiomers. False chiral. False e) All compounds with asymmetric carbon atoms are f)The relative configuration...
Which of the following chiral compounds is(are) R enantiomer(s)? 1) I. II III но, CI. Н,с CH CI OH н,с 2) You found an organic compound containing chiral carbon atom with the following four substituents: HC C-, CI-, O C- and H2C-CH-, What would be the correct order of their priorities? A) HC C-> O-C->CI-> H2C-CH B) Cl->HCC-> 0-C-> H2C-CH C) Cl-> O C-> HC C-> H2C-CH D) Cl-> O-C-> H2C-CH-> HC C E) O-C-> Cl-> HC C-> H2C-CH 3)...
please explain your answers
11. Indicate whether the pairs of compoun whether the pairs of compounds shown below are enantiomers, diastereomers, structural (constit. ructural constitutional) isomers, the same compound, or different compounds which are not isomers. (0.25 pts ea = 1 pt) Structural H OH Vs. constitutional но н OH CHE H OH vs. dia stereomers BE BroH. H₂CH₂CH CH3 HOCH2 CHO here the we dia stereomers distoremos он он носна сно н CNHO VS HOC 2 TNH₂ CH SH...
please go into detail (about S and R configuration) as im having
difficulty with this.
thanks
achiral 5.58 Draw bond-line structures using wedges and dashes for the following compounds: 5. rel CHE НЕОН Нонн нон (а) Сн, Et Н -ОН НО-Ен нон (b) Me Et HO- H НЕОН Нон Me (а) (c) 5.6 Me me Н но (d) Me -СІ -н Me CI- НО (e) H -н Me 5.6. 5.59 The following questions apply to the five compounds in the...
7. How are these two compounds related to each other: same compound, structural isomers, enantiomers diastereomers? сH, сн, Answer OH HO н- H он но -н Н- CH, CH, 8. How are these two compounds related to each other: same compound, structural isomers, enantiomers, diastereomers? сH,он CH,OH Answer: Но Н- Он н Н OH но- -н CH сH, 9. (R)-tartaric acid has a specific rotation of +12.0 degrees. a) What is the specific rotation of (S)-tartaric acid? b) What is...
5. (3 pts each) For the following pairs of molecules, indicate if they are identical different compounds. enantiomers, diastereomers, or constitutional isomers CHE CH H3COH and HOT но — сня нас — Br Hc- Br CH2OH Леон нон он and a нус он Он но- нс сня CI HOBO но and нстве
1. Use VSEPR theory to predict the molecular geometry for each of the following molecules, indicate whether each bond in it is a a or m bond, and provide the hybridization scheme for each non-hydrogen atom а. Н.С %3 снCH %3D CH, b. (носн»),С(СH,)соон с. CH,соосH(CHә)сн — снс 3D ссн, e. (CH3),СHCH,CH(NH,)C0OH d. CH,онсH(NH,)соон 2. Write the resonance structures and resonance hybrid for each of the following ions. Use curved arrows to show the shifts in electrons. ь. CH3 d....
biochem
7. Indicate whether each of the following carbohydrates is reducing or nonreducing: HO GHOH он нонни У SH,OH cң он HỌ O OCH е ну о чно он НА но то он (c) HOCHZ0. ÇH,OH ну CH,OH а, ОЛОН 4 на Xно- ньон yoXч на ко, ОН Н
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