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1. (a) Draw the most stable conformer of the following molecule and explain its stability. F-CH2-CH2-OH (b) How do you separate optically active benzoic acid from its racemic mixture? (c) Assign the R/S or E/Z nomenclature of the following molecules. i) 。་ཚིག་" COOH H3C. ii) H CH3 Br RIS

1. (a) Draw the most stable conformer of the following molecule and explain its stability. F-CH2-CH2-OH (b) How do you separate optically active benzoic acid from its racemic mixture? (c) Assign the R/S or E/Z nomenclature of the following molecules. i) 。་ཚིག་" COOH H3C. ii) H CH3 Br RIS

Biochemistry
Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
Section: Chapter Questions
Problem 1P
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1. (a) Draw the most stable conformer of the following molecule and explain its stability. F-CH2-CH2-OH (b) How do you separate optically active benzoic acid from its racemic mixture? (c) Assign the R/S or E/Z nomenclature of the following molecules. i) 。་ཚིག་" COOH H3C. ii) H CH3 Br RIS
Transcribed Image Text:1. (a) Draw the most stable conformer of the following molecule and explain its stability. F-CH2-CH2-OH (b) How do you separate optically active benzoic acid from its racemic mixture? (c) Assign the R/S or E/Z nomenclature of the following molecules. i) 。་ཚིག་" COOH H3C. ii) H CH3 Br RIS
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