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Please answer parts G,H,I
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- Indicate the relationship between each pair. Choose from: configurational stereoisomers,conformers, constitutional isomers, or different formulas (Each term is used at least twice.)1) Are the molecules A and B... conformational isomers? Diastereomers? Enantiomers? Position isomers? Non-related? 2) What about the molecules B and C? 3) What about the molecules C and D?For each pair, indicate whether they are constitutional isomers, enantiomers, diastereoisomers, or identical molecules. A BDEF
- Is this a diastereomer, enantiomer, identical, or other? thanksBased on the image. What is 1. The anti-conformer of hexane in Newman projection. 2. The equivalent structure of LAM in sawhorse representation. 3.-Sketch the Fischer projection and make a model of each stereoisomer (R and S) of the alcohol 2-butanol, CH3CHOHCH2CH3. Also sketch the monosaccharide glyceraldehyde, HOCH2CHOHCHO. Prioritize the four groups attached to the stereocenter with 1 being the highest priority and 4 being the lowest priority.
- pls show the the isomers of butane-2,3-diol. Which pairs are enantiomers? diastereomers? mesomers? pls explain whyH3C Cl \ / C=C / \ H2N I (R)-enantiomer (Z) isomer (S)-enantiomer (E) isomer meso compoundThe [α] of pure quinine, an antimalarial drug, is −165.Calculate the ee of a solution with the following [α] values: −50, −83,and −120.For each ee, calculate the percent of each enantiomer present.What is [α] for the enantiomer of quinine?If a solution contains 80% quinine and 20% of its enantiomer, what isthe ee of the solution?What is [α] for the solution described in part (d)?
- Part D. Do the two structures A and B of each pair drawn below represent the same molecule, constitutional isomers, or stereoisomers? If A and B are stereoisomers, further classify them as enantiomers or diastereomers.Are these chiral or achiral? Is the stereo enter R(D), S(L) or neither? Please state the full name and stereocenter indicator.I need help with both parts here. An FYI if you need, Part 2 means enantiomers, diasteromers, or constitutional isomers.