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
Predict the major products of the reaction below.
![### Organic Chemistry Reaction Scheme
#### Chemical Structure
The image features an organic molecule with a bicyclic system. This system consists of a six-membered and a five-membered carbon ring. Attached to the five-membered ring is a nitrile group (–C≡N), indicating the presence of a triple bond between the carbon and nitrogen atoms.
#### Reaction Scheme
The reaction involves two steps:
1. **Step 1: EtLi (Ethyl Lithium)**
- The molecule is treated with ethyl lithium, a strong base and nucleophile, often used to add alkyl groups to substrates or to deprotonate acidic hydrogen atoms.
2. **Step 2: H₂O (Water)**
- The reaction mixture is then subjected to water. This is typically used to quench the reaction.
These steps suggest a transformation involving the nitrile group, likely leading to further functionalization of the molecule.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Faf9c4940-d1e4-43ee-8063-d776cc939584%2Ffa777f2b-e224-4e47-93e7-23263ce60909%2F9qf8d2e_processed.jpeg&w=3840&q=75)
Transcribed Image Text:### Organic Chemistry Reaction Scheme
#### Chemical Structure
The image features an organic molecule with a bicyclic system. This system consists of a six-membered and a five-membered carbon ring. Attached to the five-membered ring is a nitrile group (–C≡N), indicating the presence of a triple bond between the carbon and nitrogen atoms.
#### Reaction Scheme
The reaction involves two steps:
1. **Step 1: EtLi (Ethyl Lithium)**
- The molecule is treated with ethyl lithium, a strong base and nucleophile, often used to add alkyl groups to substrates or to deprotonate acidic hydrogen atoms.
2. **Step 2: H₂O (Water)**
- The reaction mixture is then subjected to water. This is typically used to quench the reaction.
These steps suggest a transformation involving the nitrile group, likely leading to further functionalization of the molecule.
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