`CF3 NaH DMSO

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...
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
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY