Homework Help is Here – Start Your Trial Now!
Science
Chemistry
Draw the major product of this reaction. Ignore inorganic byproducts. (CH3)3CCI (1 equiv) AICI 3 Q

Draw the major product of this reaction. Ignore inorganic byproducts. (CH3)3CCI (1 equiv) AICI 3 Q

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...
See similar textbooks
icon
Related questions
Question

Branch of C(CH3)3 was incorrect.

**Reaction Overview: Friedel-Crafts Alkylation** **Objective:** Draw the major product of the reaction. Ignore inorganic byproducts. **Starting Material:** - **Aromatic Ring:** The structure shown is benzene, a six-carbon ring with alternating double bonds. **Reagents:** - **(CH₃)₃CCl (1 equiv):** This is tert-butyl chloride, an alkyl halide with three methyl groups attached to a central carbon which is bonded to a chlorine atom. - **AlCl₃:** Aluminum chloride, a strong Lewis acid used as a catalyst. **Reaction Details:** - The reaction involves a Friedel-Crafts alkylation where the aluminum chloride helps to generate a carbocation from tert-butyl chloride. This carbocation then reacts with the benzene ring, adding the tert-butyl group to the ring. - The most common position for the substitution is the para position if substituents would be involved, but with benzene (which is symmetrical), the product will simply be benzene with a tert-butyl group attached.
Transcribed Image Text:**Reaction Overview: Friedel-Crafts Alkylation** **Objective:** Draw the major product of the reaction. Ignore inorganic byproducts. **Starting Material:** - **Aromatic Ring:** The structure shown is benzene, a six-carbon ring with alternating double bonds. **Reagents:** - **(CH₃)₃CCl (1 equiv):** This is tert-butyl chloride, an alkyl halide with three methyl groups attached to a central carbon which is bonded to a chlorine atom. - **AlCl₃:** Aluminum chloride, a strong Lewis acid used as a catalyst. **Reaction Details:** - The reaction involves a Friedel-Crafts alkylation where the aluminum chloride helps to generate a carbocation from tert-butyl chloride. This carbocation then reacts with the benzene ring, adding the tert-butyl group to the ring. - The most common position for the substitution is the para position if substituents would be involved, but with benzene (which is symmetrical), the product will simply be benzene with a tert-butyl group attached.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 3 steps with 2 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Alkanes and Cycloalkanes
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.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY
SEE MORE TEXTBOOKS