Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
Bartleby Related Questions Icon

Related questions

bartleby

Concept explainers

Question
**Curved Arrow Mechanism for the Reaction**

In this reaction, you are asked to provide a curved arrow mechanism for the given chemical transformation. The reactant is a compound with an iodine (I) atom, and it reacts with sodium chloride (NaCl) to produce a compound where chlorine (Cl) is substituted in place of iodine.

### Reaction Steps:

1. **Reactant Description**: The starting material is an organic compound with an iodide group attached to a carbon atom. The structure shows three carbon branches.

2. **Reaction Process**: 
   - The iodide ion (I-) will leave, forming a carbocation intermediate. 
   - The chloride ion (Cl-) from NaCl will then attack the carbocation, replacing the iodine with chlorine.

3. **Product Description**: The final product is similar to the original compound, except the iodine atom has been replaced by a chlorine atom.

### Explanation:

- **Curved Arrows**: Use curved arrows to show the movement of electrons. 
  - One arrow should depict the departure of the iodine atom, indicating the formation of the carbocation.
  - Another arrow should show the attack of the chloride ion on the carbocation, leading to the substitution.

This kind of reaction illustrates a typical nucleophilic substitution process in organic chemistry, specifically an SN1 mechanism, where the leaving group departs before the nucleophile attacks.
expand button
Transcribed Image Text:**Curved Arrow Mechanism for the Reaction** In this reaction, you are asked to provide a curved arrow mechanism for the given chemical transformation. The reactant is a compound with an iodine (I) atom, and it reacts with sodium chloride (NaCl) to produce a compound where chlorine (Cl) is substituted in place of iodine. ### Reaction Steps: 1. **Reactant Description**: The starting material is an organic compound with an iodide group attached to a carbon atom. The structure shows three carbon branches. 2. **Reaction Process**: - The iodide ion (I-) will leave, forming a carbocation intermediate. - The chloride ion (Cl-) from NaCl will then attack the carbocation, replacing the iodine with chlorine. 3. **Product Description**: The final product is similar to the original compound, except the iodine atom has been replaced by a chlorine atom. ### Explanation: - **Curved Arrows**: Use curved arrows to show the movement of electrons. - One arrow should depict the departure of the iodine atom, indicating the formation of the carbocation. - Another arrow should show the attack of the chloride ion on the carbocation, leading to the substitution. This kind of reaction illustrates a typical nucleophilic substitution process in organic chemistry, specifically an SN1 mechanism, where the leaving group departs before the nucleophile attacks.
Expert Solution
Check Mark
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY