1 draw the stereoisomers of the following amino acids, indicate pairs of enantiomers and pairs of diastereomers .(a) .CH3CHCH2-----CHCOO^-
I I
CH3 ^+NH3
LEUCINE
(b) CH3CH2CH-CHCOO^-
I I
CH3 - +NH3
1 draw the stereoisomers of the following amino acids, indicate pairs of enantiomers and pairs...
stereoisomers of the following below. Label all chirality, indicate any enantiomers and/or diastereomers. a. Amino Acid Leucine CH,CHCH2çit code CH3 ENita b. 2-methyl-1-cyclohexanol
2. For each of the pairs of compounds, indicate if they are identical, enantiomers, diastereomers, constitutional isomers or different compounds. Z-bromopropaneitrite Br CN constitutional isomers H2CH... CN CH3 CH3 COH Hanc HC HEN HS o n diastereomers MMCH₂CH₃ CH3 3. Identify the chiral centers in the diastereomers below and label each as Ror S. CHE
Are the following pairs identical, enantiomers, diastereomers, or constitutional isomers? Sort these pairs into the proper categories. Are the following pairs identical, enantiomers, diastereomers, or constitutional isomers? Sort these pairs into the proper categories. Reset Help HC=CH2 CH2CH3 CH3 and CH3CH2H U CH,OH CHCH H-CH3 and CHH CH2CH3 CH OH CH3 HOCHZ H HC=CH2 CH3 CH3 CH,CH, CH3 CH,CH3 Ho-H ood HO-FH || - ci and H- C1 CH2CH3 HOH and H-OH H- Cland CiH CH3 CH and CH3 and...
In-lab Discussion Questions 1. These four stereoisomers constitute 2 pairs of enantiomers, or mirror images. Using the R, S labeling system (see box below for review), name each of the diastereomers. The basic name is 2,3-dibromo-3-phenylpropanoic acid. 2. Which pairs of compounds are enantiomers? 3. Which pairs of compounds are diastereomers? н Br o Br Ho H Bro Br но Хон Х ОН он он н Br Br' H Br' н. н Br stereoisomer 1 stereoisomer 2 stereoisomer 3 stereoisomer...
Draw ALL unique stereoisomers for the following structure and label ALL stereoisomeric relationships (enantiomers and diastereomers).
Enantiomer - R - R Extra Credit: 10 pts. Draw all the stereoisomers of the following convention. Identify all pairs of enantiomers ng molecule Label all sterecenie carbons using the and diastereomers (Hint: Rings have geometrie some
1) a) Using Fischer projections or perspective formulas, draw the stereoisomers obtained from the following reaction: Q.1 (5) trans-3-hexene + Cl2 → b) Indicate the stereochemical relationship of the products (enantiomers, diastereomers or identical).
Indicate whether each of the following pairs of compounds are identical, enantiomers, diastereomers, or constitutional isomers. 'HD and a
1. Consider the following Fischer projection formulas of 3-amino-2-butanol. Decide which pairs of the formulas are related as enantiomers, which are related as diastereomers, and which represent identical molecules. Assign R or S absolute configuration to C2 and C3 for each structure, and then decide. List your results by letters in the spaces provided below. (5 pts) CH2CH3 O CH3CH2 - NH căH HS CH2CH3 H. NH2 SH CH3CH2CH CH,CH2 C- NH, SH Enantiomeric pairs: Diastereomeric pairs: Identical molecules:
Four stereoisomers of a compound are given below. Classify the following pair of molecules as enantiomers or diastereomers. Drag the appropriate items to their respective bins. (options to drag to the bins are as follow: (A) Structures I & II (B) Structures I & III (C) Structures III & IV (D) I & IV (E) II & IV (F) II & III Bins include: Enantiomers Diastereomers Four stereoisomers of a compound are given below. Classify the following pair of molecules as enantiomers or diastereomers. Drag the appropriate items...