`CF3 NaH DMSO

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter8: Haloalkanes, Halogenation, And Radical Reactions
Section8.7: Radical Autoxidation
Problem CQ
icon
Related questions
icon
Concept explainers
Question

Draw the products. If more than one product is formed determine which one is the major one. 

This image depicts a chemical reaction scheme involving an organic molecule under specific reaction conditions. 

The structure on the left side of the arrow is a chemical compound identified as a cyclohexane derivative with a triflate (trifluoromethanesulfonate) group attached. The cyclohexane ring has substituents, including a triflate group (O=S=O group attached to a CF3), a methyl group, and other unspecified hydrogen atoms.

The reaction conditions are indicated above and below the arrow pointing to the right:
- Reagent: Sodium hydride (NaH)
- Solvent: Dimethyl sulfoxide (DMSO)

This combination of sodium hydride in DMSO suggests it might be a deprotonation reaction, possibly leading to the formation of an intermediate compound or a subsequent reaction step. 

This kind of reaction scheme is vital in organic chemistry to illustrate the transformation of molecules under controlled laboratory conditions, highlighting the importance of reagents and solvents in driving chemical reactions.
Transcribed Image Text:This image depicts a chemical reaction scheme involving an organic molecule under specific reaction conditions. The structure on the left side of the arrow is a chemical compound identified as a cyclohexane derivative with a triflate (trifluoromethanesulfonate) group attached. The cyclohexane ring has substituents, including a triflate group (O=S=O group attached to a CF3), a methyl group, and other unspecified hydrogen atoms. The reaction conditions are indicated above and below the arrow pointing to the right: - Reagent: Sodium hydride (NaH) - Solvent: Dimethyl sulfoxide (DMSO) This combination of sodium hydride in DMSO suggests it might be a deprotonation reaction, possibly leading to the formation of an intermediate compound or a subsequent reaction step. This kind of reaction scheme is vital in organic chemistry to illustrate the transformation of molecules under controlled laboratory conditions, highlighting the importance of reagents and solvents in driving chemical reactions.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 1 images

Blurred answer
Knowledge Booster
Ionic Equilibrium
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305580350
Author:
William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305080485
Author:
John E. McMurry
Publisher:
Cengage Learning