/*! 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} Q47P Draw the elimination products th... [FREE SOLUTION] | 91影视

91影视

Log out

Learning Materials

Features

Discover

Chapter 9: Q47P (page 435)

Draw the elimination products that are formed when 3-bromo-3-methyl-1-butene reacts with

Short Answer

Expert verified

The products are given below,

Step by step solution

01

Definition of elimination reaction

Elimination reaction is basically a reaction between alkyl bromide and a base in a step-by-step manner or in a concerted mechanism of bond breaking and making. During the elimination reaction, The C-X (X=halogen) and C-H bond should be in anti-periplanar fashion.

Example: E1, E2 E1cB mechanism.

02

Products of elimination

a) In case of the 1st one, as the CH3O- is strong, it can undergo elimination reaction through E2 mechanism.

E2 mechanism

b) CH3OH being a weak base, it can undergo reaction through E2 mechanism.


These are the elimination products.

Noted that in both of the cases, the products are same.

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

Which compound is more reactive in an SN1 reaction? In each case, you can assume that both alkyl halides have the same stability.

What products are formed from the following reactions?

Draw the stereoisomers that are formed from the following SN1 reactions:

a. 3-bromo-3-methylpentane and methanol

b. 3-chloro-3-methylhexane and methanol

tert-Butyl chloride undergoes solvolysis in both acetic acid and formic acid. Solvolysis occurs 5000 times faster in one of these two solvents than in

the other. In which solvent is solvolysis faster? Explain your answer. (Hint: Formic acid is more polar than acetic acid.)

Which reactant in each of the following pairs undergoes an elimination reaction more rapidly? Explain your choice.
See all solutions

Recommended explanations on Chemistry Textbooks

Chemical Analysis

Read Explanation

Physical Chemistry

Read Explanation

Inorganic Chemistry

Read Explanation

Chemistry Branches

Read Explanation

Ionic and Molecular Compounds

Read Explanation

Making Measurements

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.