Part A1. Determine the absolute configuration (Ror S) of the stereogenic centre incompounds (1) & (II) below.(i)HOHH₂CCH 3BrH(II)HO2. A compound may have a number ofpossible stereoisomers which isdetermined with the formula 2 (n =number of stereocentres). The compound(-)-menthone (below) is a Natural Productfound in peppermint. Use the formulagiven to determine the number of possiblestereoisomers in this compound can have.ICHOHCH₂CH3CH(CH3)2

For the absolute configuration of the molecules , we use the following rules ; For fisher…

Part A 1. Determine the absolute configuration (R or S) of the stereogenic centre in compounds (1) & (II) below. (i) HO H H₂C CH3 Br H (II) HO 2. A compound may have a number of possible stereoisomers which is determined with the formula 2n (n = number of stereocentres). The compound (-)-menthone (below) is a Natural Product found in peppermint. Use the formula given to determine the number of possible stereoisomers in this compound can have. H CHO H CH₂CH3 CH(CH3)2

Part A 1. Determine the absolute configuration (R or S) of the stereogenic centre in compounds (1) & (II) below. (i) HO H H₂C CH3 Br H (II) HO 2. A compound may have a number of possible stereoisomers which is determined with the formula 2n (n = number of stereocentres). The compound (-)-menthone (below) is a Natural Product found in peppermint. Use the formula given to determine the number of possible stereoisomers in this compound can have. H CHO H CH₂CH3 CH(CH3)2

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 23E: up an example (not appearing in this ChemActivity) of a pair of molecules that are a)constitutional...

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