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QUESTION 8 What is the major product of the following reaction? "OCH3 a. Ob. d. O e.

QUESTION 8 What is the major product of the following reaction? "OCH3 a. Ob. d. O e.

Chemistry
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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**Question 8** What is the major product of the following reaction? The reaction involves a chlorinated alkane substrate reacting with methoxide ion (\(-OCH_3\)). The substrate structure on the left shows a tertiary carbon with a chlorine atom attached. Above this carbon, there is a bold wedge indicating a group pointing outwards, and there is a methyl group attached to this tertiary carbon. It appears to be a potential elimination reaction involving methoxide ion (\(-OCH_3\)) as the base. Five options (a) to (e) are provided as potential products: - **Option a:** A branched alkene with a double bond between the two end carbons on a chain. - **Option b:** A linear alkene with a double bond in the middle of the chain. - **Option c:** A linear alkene similar to option b but with different stereochemistry. - **Option d:** Similar to option a, but with a different stereochemistry of the double bond. - **Option e:** A branched alkene with a double bond on a different position than in a. Each option reflects different positions and stereochemistry of the potential double bond formed during the elimination reaction.
Transcribed Image Text:**Question 8** What is the major product of the following reaction? The reaction involves a chlorinated alkane substrate reacting with methoxide ion (\(-OCH_3\)). The substrate structure on the left shows a tertiary carbon with a chlorine atom attached. Above this carbon, there is a bold wedge indicating a group pointing outwards, and there is a methyl group attached to this tertiary carbon. It appears to be a potential elimination reaction involving methoxide ion (\(-OCH_3\)) as the base. Five options (a) to (e) are provided as potential products: - **Option a:** A branched alkene with a double bond between the two end carbons on a chain. - **Option b:** A linear alkene with a double bond in the middle of the chain. - **Option c:** A linear alkene similar to option b but with different stereochemistry. - **Option d:** Similar to option a, but with a different stereochemistry of the double bond. - **Option e:** A branched alkene with a double bond on a different position than in a. Each option reflects different positions and stereochemistry of the potential double bond formed during the elimination reaction.
**QUESTION 22** What is the major organic product for the following reaction? \[ \text{CH}_3\text{CH}_2\text{CH}(\text{OH})\text{CH}_2\text{CH}_3 \xrightarrow{\text{H}^+} \] **Options:** - a. \(\text{CH}_3\text{CH}_2\text{C}(\text{OH})\text{CH}_3\) - b. \(\text{CH}_3\text{C}=\text{CHCH}_2\text{CH}_3\) - c. \(\text{H}_2\text{C}=\text{CCH}_2\text{CH}_2\text{CH}_3\) - d. \(\text{CH}_3\text{CH}_2\text{C}=\text{CH}_2\) - e. \(\text{CH}_3\text{CHCH}=\text{CHCH}_3\)
Transcribed Image Text:**QUESTION 22** What is the major organic product for the following reaction? \[ \text{CH}_3\text{CH}_2\text{CH}(\text{OH})\text{CH}_2\text{CH}_3 \xrightarrow{\text{H}^+} \] **Options:** - a. \(\text{CH}_3\text{CH}_2\text{C}(\text{OH})\text{CH}_3\) - b. \(\text{CH}_3\text{C}=\text{CHCH}_2\text{CH}_3\) - c. \(\text{H}_2\text{C}=\text{CCH}_2\text{CH}_2\text{CH}_3\) - d. \(\text{CH}_3\text{CH}_2\text{C}=\text{CH}_2\) - e. \(\text{CH}_3\text{CHCH}=\text{CHCH}_3\)
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