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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please help with the following question:
Draw a structural formula for the major organic product AND intermediate of the following reaction:
![### Organic Chemistry Reaction - Structural Formula of Major Product
**Problem Statement:**
Draw a structural formula for the major organic product of the following reaction:
**Reaction:**
\[ \text{CH}_3\text{CH}=\text{CHCH}_2\text{CH}_3 \ + \ \text{Cl}_2 \rightarrow \text{CH}_2\text{Cl}_2 \]
**Explanation:**
This reaction involves the addition of chlorine (Cl₂) to an alkene (CH₃CH=CHCH₂CH₃). The double bond between carbon atoms in the alkene reacts with chlorine, resulting in the formation of a vicinal dihalide (a compound with two halogens attached to adjacent carbons).
**Structural Formula:**
When chlorine adds to the 3-pentene (CH₃CH=CHCH₂CH₃), the double bond breaks, and each chlorine atom attaches to one of the carbons that were formerly double-bonded. The major product formed is 3,4-dichloropentane:
\[ \text{CH}_3\text{CH}(\text{Cl})\text{CH}(\text{Cl})\text{CH}_2\text{CH}_3 \]
This process is representative of an electrophilic addition reaction, commonly seen in organic chemistry involving alkenes and halogens.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F94f2b720-6c17-4283-96f9-864e0b1ece0e%2F9e103039-1a75-48d1-a72b-6d879a0ba714%2Fjbi3y3h_processed.jpeg&w=3840&q=75)
Transcribed Image Text:### Organic Chemistry Reaction - Structural Formula of Major Product
**Problem Statement:**
Draw a structural formula for the major organic product of the following reaction:
**Reaction:**
\[ \text{CH}_3\text{CH}=\text{CHCH}_2\text{CH}_3 \ + \ \text{Cl}_2 \rightarrow \text{CH}_2\text{Cl}_2 \]
**Explanation:**
This reaction involves the addition of chlorine (Cl₂) to an alkene (CH₃CH=CHCH₂CH₃). The double bond between carbon atoms in the alkene reacts with chlorine, resulting in the formation of a vicinal dihalide (a compound with two halogens attached to adjacent carbons).
**Structural Formula:**
When chlorine adds to the 3-pentene (CH₃CH=CHCH₂CH₃), the double bond breaks, and each chlorine atom attaches to one of the carbons that were formerly double-bonded. The major product formed is 3,4-dichloropentane:
\[ \text{CH}_3\text{CH}(\text{Cl})\text{CH}(\text{Cl})\text{CH}_2\text{CH}_3 \]
This process is representative of an electrophilic addition reaction, commonly seen in organic chemistry involving alkenes and halogens.
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