5. State how each pair of compounds is related. Are they enantiomers (E), diastereomers (D), constitut...
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...
state how each pair of compound is related. Are they enantiomers,diastereomer,constitutional isomers, or identical. CH3 CH3 HO- H H- Н НО ОН Н Н -СІ СІ
D. Specify whether each pair of structures below are constitutional isomers, identical, enantiomers, diastereomers or not related. (3 pts) A. ОН ОН Он OH В. ОН но
Select the single best answer. How are the compounds in the following pair related to each other? Are they identical, enantiomers, diastereomers, or constitutional isomers of each other? and OH HO HO OH diastereomers O constitutional isomers enantiomers identical
но OH prortacyelin 8.(10 points)Label each pair of stereoisomers below as: enantiomers b. diastereomers c. identical Place the letter of the correct answer in the blank to the left of the pair of stereoisomers. a. Нс Нс OH HO Н H Cн-он Но CH-он c0,н но-- Нос H но CH3 CH3 нос но-с.. «сон CO2H
need help with 21-24 21. Label each of the following compounds as "meso" or "not meso." (1 pt) он он Br Он он Ән The following problems are about Fischer projections. Watch the Chapter 5 Conclusion Video and read section 5.7 in the Klein textbook before you continue. 22. Assign the following stereocenter as having the Ror S absolute configuration (1 pt) он HEEt 23. Are the following compounds enantiomers, diastereomers, identical, or constitutional isomers? (1 pt) но -н нон...
please explain your answers 11. Indicate whether the pairs of compounds shown below are enantiomers, diastereomers, structural (constitutional) isomers, the same compound, or different compounds which are not isomers. (0.25 pts ea = 1 pt) vs. нон Но н. он он HOCHS HT CH3 C vs. Broh H₃CH НОСН2СНО нон нон H How HOCH CHO н JONH2 NH2 HOC CH2SH HSCHE CO2H
4. Label each pair of stereoisomers below as A,B,C,D a. Enantiomers b. Diastereomers c. Identical d. Meso Compounds a 5 diasteromers e nannamers OH ОН
2. Label each of the following pairs of molecules as enantiomers, diastereomers, meso compounds, or constitutional isomers. Some terms may be used more than once, and some terms may not be used at all. The use of the model kit is GREATLY encouraged for this question (5 points). CH3 ОН ОН \ 'NTOH о он Нонно- нон н он / он но CH3 H3G ног он гун, 3 H3CCH3 HONH2 - тр H2N " он он сна он он NH2
4) For each pair of structures, determine if they enantiomers (E), diastereomers (D), or None (N). (12 pts) are identical (I), structural isomers (SI), conformers (C), a) b) Br HJ CH3 Нас. F F Fl Br H CH3 CH3 F F c) d) но но CI 4) Below are Newman projection representations for (2R,3R)-, (2S,3S)- and (2R,3S)- stereoisomers of