Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question
![A) methyllithium
Ph
Ph
7. What alkyllithium would react with acetic acid to form 2-butanone?
MECHANISMS
Ph
CO,H
8. An ylide is a molecule that can be described as a:
H
B) vinyllithium
CH3
1. SOCI₂
2. LIAI[OC(CH3)3]3H
C) ethyllithium
or
H
1. Using Newman projections, show the preferred conformations of the betaine and oxaphosphatane intermedia
In the following reaction.
D) propyllithium
A) carbanion bound to a negatively charged heteroatom.
B) carbocation bound to a positively charged heteroatom.
C) carbocation bound to a carbon radical.
D) carbocation bound to a diazonium ion.
E) carbanion bound to a positively charged heteroatom.
E) phenyllithium](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F65d4d6a4-c190-4762-a5ec-7b8c8c6bb63b%2F423cd603-0a08-4b8c-ba9d-eda171174bb5%2Fza200gp_processed.jpeg&w=3840&q=75)
Transcribed Image Text:A) methyllithium
Ph
Ph
7. What alkyllithium would react with acetic acid to form 2-butanone?
MECHANISMS
Ph
CO,H
8. An ylide is a molecule that can be described as a:
H
B) vinyllithium
CH3
1. SOCI₂
2. LIAI[OC(CH3)3]3H
C) ethyllithium
or
H
1. Using Newman projections, show the preferred conformations of the betaine and oxaphosphatane intermedia
In the following reaction.
D) propyllithium
A) carbanion bound to a negatively charged heteroatom.
B) carbocation bound to a positively charged heteroatom.
C) carbocation bound to a carbon radical.
D) carbocation bound to a diazonium ion.
E) carbanion bound to a positively charged heteroatom.
E) phenyllithium
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