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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Transcribed Image Text:### Reaction Analysis and Questions
**For the reaction below, provide the IUPAC name of the product, and answer any additional questions.**
**Reaction Scheme:**
In the given reaction scheme, a bromocyclohexane compound with an ethyl (Et) substituent reacts with tert-Butyl sodium (t-BuONa).
**Questions:**
a. **Product's IUPAC name:**
- Provide the IUPAC name for the product formed in the reaction shown.
*Answer box:*
______________________________________
b. **What mechanism is in effect for the above reaction (SN1, SN2, E2, E1)?**
- Identify which mechanism (SN1, SN2, E2, or E1) is operative in the given reaction.
*Answer box:*
______________________________________
c. **What is the name of the regiocontrol exhibited in this reaction product (if there is no regiocontrol answer with none)?**
- Name the type of regiocontrol observed in the final reaction product. If no regiocontrol is present, indicate 'none.'
*Answer box:*
______________________________________
**Graph/Diagram Explanation:**
The diagram shows a cyclohexane ring with a bromine (Br) atom attached to one of its carbon atoms. Attached to the neighboring carbon is an ethyl group (Et). The reagent used for the reaction is tert-Butyl sodium (t-BuONa), a strong base often used in elimination reactions.
**Note:** The actual IUPAC name and mechanism may vary based on the specific conditions and reactants in the full reaction scheme. This exercise requires the learner to analyze the presented reaction and determine the resulting product's IUPAC name, the reaction mechanism, and the type of regiocontrol, if any.
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