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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![Which of the following is an intermediate in this Grignard reaction?
O 1)
H.
OH
O 2)
OH
3)
4)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F8ce81839-7946-4ae6-b34d-b631f6705172%2Fff91f24f-8c3f-4b00-abf5-0bd5a6a733fa%2F5v5uh59_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Which of the following is an intermediate in this Grignard reaction?
O 1)
H.
OH
O 2)
OH
3)
4)
![Grignard Reagent Synthesis of Triphenylmethanol
Step 3: Reaction of resulting ketone with second Grignard reagent molecule
OMBr
„MgBr
stable tetrahedral intermediate
A second Grignard reagent readily attacks the resulting ketone's carbonyl
carbon atom forming another carbon-carbon bond and permanently distorting
the carbonyl group. This resulting tetrahedral intermediate is a stable alkoxide
ion.
°o=¢](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F8ce81839-7946-4ae6-b34d-b631f6705172%2Fff91f24f-8c3f-4b00-abf5-0bd5a6a733fa%2Fmfjjtm_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Grignard Reagent Synthesis of Triphenylmethanol
Step 3: Reaction of resulting ketone with second Grignard reagent molecule
OMBr
„MgBr
stable tetrahedral intermediate
A second Grignard reagent readily attacks the resulting ketone's carbonyl
carbon atom forming another carbon-carbon bond and permanently distorting
the carbonyl group. This resulting tetrahedral intermediate is a stable alkoxide
ion.
°o=¢
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