An electrophilic addition reaction in which a trans а) isomer gives rise only to a meso product, is said to be In an S,2 reaction the nucleophile must approach the substrate opposite the leaving b) group because c) Draw the structure on the left hand of this equation: N ECH H,C (L)-Phenylalanine has an optical rotation of d) -32.7°, what is the optical rotation of (D)-phenylalanine e) Complete the equation by drawing the initial and final products of the reaction: 1. ВНЗ 2. НООН 3. NaOH -CH3

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter13: Substitution
Section: Chapter Questions
Problem 4E
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An electrophilic addition reaction in which a trans
а)
isomer gives rise only to a meso
product, is said to be
In an S2 reaction the nucleophile must approach the
substrate opposite the leaving
b)
group because
c)
Draw the structure on the left hand of this equation:
CH,
H,C
d)
-32.7°, what is the optical rotation of (D)-phenylalanine
(L)-Phenylalanine has an optical rotation of
e)
Complete the equation by drawing the initial and final
products of the reaction:
1. BH3
2. НООН
3. NaOH
CH3
Transcribed Image Text:An electrophilic addition reaction in which a trans а) isomer gives rise only to a meso product, is said to be In an S2 reaction the nucleophile must approach the substrate opposite the leaving b) group because c) Draw the structure on the left hand of this equation: CH, H,C d) -32.7°, what is the optical rotation of (D)-phenylalanine (L)-Phenylalanine has an optical rotation of e) Complete the equation by drawing the initial and final products of the reaction: 1. BH3 2. НООН 3. NaOH CH3
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