For the dehydrohalogenation (E2) reaction shown, draw the Zaitsev product(s) resulting from elimination involving C2–C3 (i.e., the carbon atoms depicted with stereobonds). Show the product stereochemistry clearly. If there is more than one organic product, both products may be drawn in the same box. Ignore elimination involving C2 or C3 and any carbon atom other than C3 or C2.
For the dehydrohalogenation (E2) reaction shown, draw the Zaitsev product(s) resulting from elimination involving C2–C3 (i.e., the carbon atoms depicted with stereobonds). Show the product stereochemistry clearly. If there is more than one organic product, both products may be drawn in the same box. Ignore elimination involving C2 or C3 and any carbon atom other than C3 or C2.
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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there is supposed to be two products here
Transcribed Image Text:**Organic Chemistry**
*Maxwell*
*Presented by Macmillan Learning*
For the dehydrohalogenation (E2) reaction shown, draw the Zaitsev product(s) resulting from elimination involving C2–C3 (i.e., the carbon atoms depicted with stereobonds). Show the product stereochemistry clearly. If there is more than one organic product, both products may be drawn in the same box. Ignore elimination involving C2 or C3 and any carbon atom other than C3 or C2.
**Reaction Details:**
- **Starting Material:** The starting organic compound contains a chlorine (Cl) atom bonded to the second carbon (C2) and hydrogen atoms bonded to adjacent carbons. Stereochemistry is depicted using wedge and dash bonds to illustrate the 3D orientation of atoms.
- **Reagents:**
- Potassium hydroxide (KOH)
- Ethanol (EtOH)
- Heat
The reaction involves an elimination mechanism where the chlorine atom and a hydrogen atom are removed to form an alkene, favoring the formation of the more substituted (Zaitsev) alkene as the major product.
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