Designate the following compound as R or S ос‑ H3C-CCH3 Н.сон Select one: A. R В....
Draw and designate the R or S configuration for each compound. CH2CH2CH2CH3 Br CH3 H3C CH(CH3)2 NH2
7. Designate each stereogenic center with an *, label R or S, and name the following compound.
Which of the following is an diastereomer of the compound below? CW CW ito it Select one: O AI OB.I OC. IV D. Designate each of the chirality centers in the following compound as Ror S. CH3 HTCHCI HO Select one: O A. a R bR O B. a =S; b=R O C. a =S; b=S D. a =R; bus o o
Consider the following pairs of structures. Designate each chirality center as (R) or (S) and identify the relationship between them by describing them as representing enantiomors, diastereomers, constitutional isomers, or two molecules of the same compound (identical).
Which of the following structures is not a phosphoester? (А) NH (В) Ос "CH₂ НО-Р-он о О н ни ОН ОН ОН (c) NH (D) N О о" 9-ро Od-o CHz но-р-оснусн; H он Онон Select one (А)
Name the following compound. Include (R), (S), cis, or trans if appropriate 8. Name the following compound. Include (R).(S), cis, or trans if appropriate. (1 pt) H3C Br
Problem 10 Consider the following pair of structures. Designate each chirality center as (R) or (S) and identify the relationship between them by describing them as representing enantiomers, diastereomers, constitutional isomers, or two molecules of the same compound. CH,CHз CH-CHз pue CH3CH2 CH3CH2
Draw the structure(s) produced by the catalytic reduction of the following compound. (H2 is in excess.) Draw hydrogen at a chirality center and use wedge-and-dashbonds to designate the stereochemistry, if applicable.Select all that apply: The product(s) of the reaction is characterized as being: (R,R), (R,S(and/or S,R)), (S,S), (achiral), (racemic), (diastereomers), (R),(S).
Designate the chiral center in the following molecule as either R or S. НО esignate the chical center is the following aplecule as either pors.clopts) C-FM
m 2. For the following molecule, designate the R and/or S configuration at each chirality center (6p) Br CI OH