non super imposable mirror images are called as
enantiomers and the trans enantiomers are as follows
1. Draw the two enantiomers of trans-1,2-Diaminocyclohexane and assign stereochemistry (R or S) to both of...
Assign the stereochemistry (R or S) on each of chirality centers in the molecules below and draw the enantiomer of each compound.
Draw the product(s) of the Diels–Alder reaction of 1,3-butadiene with trans-1,2-dibromoethene. Use wedge-and-dash bonds to show the stereochemistry of the product(s). Include hydrogens at any chirality centers.
Assign R or S stereochemistry to the chirality centers in these Newman structures. Determine if these molecules are chiral. achiral. or meso compound
s. Assign the R or s stereochemistry to the chirality centers in ascorbic acid (vitamin C)? 4pts OH HO HO OH
6. Assign R or S stereochemistry to the chirality centers in the molecule below. (2 P! OH
2. Draw the entire mechanism for the syn- addition of bromine + trans-cinnamic acid. All stereochemistry must be shown. All chirality (R, S) must be labeled for chiral centers.
3. Draw the entire mechanism for the anti- addition of bromine + trans-cinnamic acid. All stereochemistry must be shown. All chirality (R, S) must be labeled for chiral centers.
3. Draw the entire mechanism for the anti- addition of bromine + trans-cinnamic acid. All stereochemistry must be shown. All chirality (R, S) must be labeled for chiral centers. *Use backside of paper.
please draw (trans)1,3-dimethylcyclohexane in the most stable chair conformation, and assign-EXPLAIN the stereochemistry to each chiral center.. (why S or R, assign priorities)
Cl ан Cl Cl a) Assign R or S configuration to the chirality centers in the molecules. b) For each pair of compounds, determine whether they are enantiomers, diastereoisomers and meso compounds c) Determine which compounds are optically active and which compounds are not optically active. Why? Cl ан Cl Cl a) Assign R or S configuration to the chirality centers in the molecules. b) For each pair of compounds, determine whether they are enantiomers, diastereoisomers and meso compounds c)...