When 2,2-dibromo-1-phenylpropane is heated overnight with sodium amide at 150 ∘C, the major product (after addition of water) is a different foul-smelling compound of formula C9H8. Draw out the mechanism.
When 2,2-dibromo-1-phenylpropane is heated overnight with sodium amide at 150 ∘C, the major product (after addition of water) is a different foul-smelling compound of formula C9H8. Draw out the mechanism.
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:
When 2,2-dibromo-1-phenylpropane is heated overnight with sodium amide at 150 ∘C, the major product (after addition of water) is a different foul-smelling compound of formula C9H8.
Draw out the mechanism.
![I Review I Constants I Periodic Table
When 2,2-dibromo-1-phenylpropane is heated overnight with
sodium amide at 150 °C, the major product (after addition of
water) is a different foul-smelling compound of formula
C9 H8.
Part B
Give a mechanism to account for its formation.
Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds.
Add charges where needed. Electron flow arrows should start on the electron(s) of an atom or a bond and should end on an atom,
bond, or location where a new bond should be created.
H
S
:Br:
CI
CH
Br
NH2
F
[1]
Submit
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Transcribed Image Text:I Review I Constants I Periodic Table
When 2,2-dibromo-1-phenylpropane is heated overnight with
sodium amide at 150 °C, the major product (after addition of
water) is a different foul-smelling compound of formula
C9 H8.
Part B
Give a mechanism to account for its formation.
Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds.
Add charges where needed. Electron flow arrows should start on the electron(s) of an atom or a bond and should end on an atom,
bond, or location where a new bond should be created.
H
S
:Br:
CI
CH
Br
NH2
F
[1]
Submit
Previous Answers Request Answer
X Incorrect; Try Again; 11 attempts remaining
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