**Question 1:**Circle the substrate that will *not* result in a tertiary alkyl chloride when treated with HCl.- **Option A:** ![Cyclopentene](https://your-image-link-here) - **Option B:** ![2-Methylcyclopentene](https://your-image-link-here)- **Option C:** ![1-Hexene](https://your-image-link-here)**Question 2:**Circle the alkene that can be most easily formed under unimolecular elimination.- **Option A:** ![3-Methyl-2-pentene](https://your-image-link-here)- **Option B:** ![1,3-Dimethylcyclohexene](https://your-image-link-here)- **Option C:** ![Hex-3-ene](https://your-image-link-here)**Question 3:**Circle the alkene that is most electron-rich.- **Option A:** ![Methyloxolane](https://your-image-link-here)- **Option B:** ![Oxirane with Methyl Group](https://your-image-link-here)- **Option C:** ![Propenal](https://your-image-link-here)**Question 4:**Circle the conformation (as drawn) that will most rapidly undergo E2.- **Option A:** ![1-Iodo-1-phenylethane](https://your-image-link-here) - **Option B:** ![1-Iodo-2-phenylpropane](https://your-image-link-here)- **Option C:** ![2-Iodo-1-phenylethane](https://your-image-link-here)**Question 5:**Circle the most electron-rich alkene.- **Option A:** ![2-Methyl-2-butene](https://your-image-link-here)- **Option B:** ![3-Methylbut-1-ene](https://your-image-link-here)- **Option C:** ![1-Butyne](https://your-image-link-here)**Question 6:**Circle the most stable alkene.- **Option A:** ![1,2-Dimethylcycl

Answered: Image /qna-images/answer/3a0fff7a-a6c3-4e7c-9b80-ba4e17ad630c.jpg

1. Circle the substrate that will not result in a tertiary alkyl chloride when treated with HCI. A В C Me Me- 2. Circle the alkene that can be most easily formed under unimolecular elimination. A В int Me. Me „Me Me Me Me Me Me 3. Circle the alkene that is most electron rich. A B Me Me Me Me Me -Me Ме Me 4. Circle the conformation (as drawn) that will most rapidly undergo E2. A В H3C H Ph Ph Ph Ph H Ph Ph CH3 H3c H 5. Circle the most electron rich alkene. A Me „Me Ме. Me Me Me Me Me 6. Circle the most stable alkene. А Me B Me C Me. Me Me Me Ме -Me -Me `Me

1. Circle the substrate that will not result in a tertiary alkyl chloride when treated with HCI. A В C Me Me- 2. Circle the alkene that can be most easily formed under unimolecular elimination. A В int Me. Me „Me Me Me Me Me Me 3. Circle the alkene that is most electron rich. A B Me Me Me Me Me -Me Ме Me 4. Circle the conformation (as drawn) that will most rapidly undergo E2. A В H3C H Ph Ph Ph Ph H Ph Ph CH3 H3c H 5. Circle the most electron rich alkene. A Me „Me Ме. Me Me Me Me Me 6. Circle the most stable alkene. А Me B Me C Me. Me Me Me Ме -Me -Me `Me

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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