CH₂CH:CH 2. Determine R and S configurations for the following molecules: Unbonded substituent is the dotted line (into the back of the page)

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter3: Organic Compounds: Alkanes And Their Stereochemistry
Section3.SE: Something Extra
Problem 52AP: Increased substitution around a bond leads to increased strain. Take the four substituted butanes...
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1. Energy and strain: Identify the three types of strain that contribute to the instability of cis-1-methyl-2-propylcyclopropane (below)
H
H
CH₂
CH₂CH₂CH
2. Determine R and S configurations for the following molecules: Unbonded substituent is the dotted line (into the back of the page)
Br
H
IIO C-CILCII
H
CH₂
NII C II
A
I
Br
3. What products should you expect to obtain when you react cis-1,3 butadiene with 2 propen-1-al?
COOH
с
CL
II
Transcribed Image Text:1. Energy and strain: Identify the three types of strain that contribute to the instability of cis-1-methyl-2-propylcyclopropane (below) H H CH₂ CH₂CH₂CH 2. Determine R and S configurations for the following molecules: Unbonded substituent is the dotted line (into the back of the page) Br H IIO C-CILCII H CH₂ NII C II A I Br 3. What products should you expect to obtain when you react cis-1,3 butadiene with 2 propen-1-al? COOH с CL II
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