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Q: a) Determine the absolute configuration of the chiral carbons in the following molecule: CHO H- HO-…
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Q: What are the configurations of carbons 2 and 3 in the Fischer projection below? CH A. 2R, 3R B. 2R,…
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Q: The configuration in following molecule is: он No chiral center S 50% (R) & 50% (S) R
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solve the last 3 parts, g, h, and i
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- How are they identical, if in the first newman projection CH3 and CH3 are opposite from each other, but then in the second newman projection Br and CH3 are opposite from each other. Wouldnt they be diastereomers since one of the chiral centers changed?A) For a molecule with three chiral carbons the possible number of stereoisomers is: 4, 8, 6 or 2 B)Which of the following has a S configuration: (Image)To the following statement, answer true or false and explain your answer. Q) All chiral centers are also stereocenters.