Question

the single bed and single and to two Hatomis ed that the church w CC has a hicher to m e than . The over are determined by the set of w eb www the attachment H H ) for the CH Hote substituent, and IC.C. ) for the CH C H . There first priority. CH CHCH, is second and H is third these substituents are arranged rock with the owne pointing away, the configuration is d e weten is (8)-3-methylhex-1-ene. l wen wete name of the molecule PROBLEM C.10 What is the configuration, R or S. of the chiral center in each of the following molecules? NO (c) C.1c Fischer Projections and the R/S Designations Recall from Section 5.6 that vertical bonds in a Fischer projection point you and horizontal bonds point toward you. Therefore, if the lowest prior on a vertical bond, then the projection represents a properly oriented lowest-priority substituent is on a horizontal bond, instead, then it pour and, prior to assigning the configuration, we can simply reverse the ord,

Answer 1

Br (S)-4-bromo-2-methylhex-2-ene (R)-2,2,3-trimethylpentane R N NO2 (S)-2-methylbut-3-ynenitrile (R)-6-methyl-4-nitrohept-5-en-1-yne R NO2 (R)-7-methyl-5-nitrooct-6-en-1-yne