OHCH3SOCI₂CH₂Pyridine le bass!Which will best explain why the reaction is not likely to happen?Select the correct response(s):Thionyl chloride is a good reagent for primary halides.The substrate is a secondary halide.The substrate is a tertiary halide.Thionyl chloride is a good reagent for secondary halides.The solvent is polar aprotic.The solvent is polar protic

Answered: Image /qna-images/answer/d41da352-bf62-447b-ac3e-b234ce9eaf6f.jpg

Answered: CH3 SOCI fou -CH₂ Pyridine la bass!…

CH3 SOCI fou -CH₂ Pyridine la bass! Which will best explain why the reaction is not likely to Select the correct response(s): Thionyl chloride is a good reagent for primary OH

Pushing Electrons

4th Edition

ISBN:9781133951889

Author:Weeks, Daniel P.

Publisher:Weeks, Daniel P.

Chapter3: Mechanisms

Section: Chapter Questions

Problem 129EQ

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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

OH
CH3
SOCI₂
CH₂
Pyridine le bass!
Which will best explain why the reaction is not likely to happen?
Select the correct response(s):
Thionyl chloride is a good reagent for primary halides.
The substrate is a secondary halide.
The substrate is a tertiary halide.
Thionyl chloride is a good reagent for secondary halides.
The solvent is polar aprotic.
The solvent is polar protic

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