/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} 35 P What is the major product formed... [FREE SOLUTION] | 91影视

91影视

Log out

Learning Materials

Features

Discover

Chapter 18: 35 P (page 721)

What is the major product formed by an intramolecular Friedel鈥揅rafts acylation of the following compound?

Short Answer

Expert verified

The major product formed is as follows:

Step by step solution

01

Friedel-Craft acylation

Friedel-Craft acylation involves the action of an acetyl halide on an aromatic compound in the presence of anhydrous chloride.

02

Reaction

The 2D structure of the given 3D structure is as follows:

The given molecule contains two benzene rings, with one of them containing an electron releasing group -OCH3.

Acylation is more favorable toward the benzene ring, which is an electron-releasing group.

Therefore, the product of the reaction is given as follows:

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Draw the products of each reaction.

Draw the products of each reaction.

For each N-substituted benzene, predict whether the compound reacts faster than, slower than, or at a similar rate to benzene in electrophilic aromatic substitution. Then draw the major product (s) formed when each compound reacts with a general electrophile E+.

Question: Ibufenac, a para-disubstituted arene with the structure HO2CCH2C6H4CH2CH(CH3)2, is a much more potent analgesic than aspirin, but it was never sold commercially because it caused liver toxicity in some clinical trials. Devise a synthesis of ibufenac from benzene and organic halides having fewer than five carbons.

Draw the products formed when A and B are treated with each of the following reagents:

(a)Br2,FeBr3; (b)HNO3,H2SO4l3; (c) CH3CH2COCl, AlCl3
See all solutions

Recommended explanations on Chemistry Textbooks

The Earths Atmosphere

Read Explanation

Making Measurements

Read Explanation

Chemistry Branches

Read Explanation

Ionic and Molecular Compounds

Read Explanation

Chemical Analysis

Read Explanation

Nuclear Chemistry

Read Explanation
View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.