/*! 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} 46bE Which reaction in each of the fo... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

Which reaction in each of the following pairs would you expect to be faster?

(b) Thedisplacement byon bromoethane or on bromocyclohexane

Short Answer

Expert verified

Bromoethaneis​â¶Ä„show fast reaction than bromocyclohexane

Step by step solution

01

SN2reaction

It is a nucleophilic substitution reaction in which an old bond is broken, and a new bond is formed. Bothprocessesco-occur. Hence, it’s a single-step reaction.

The two reacting species are involved in the rate-determining steps.

02

Nucleophile

Nucleophiles are the negatively charged ions or the neutral species having the lone pair of electrons ready for bonding.

03

Species react faster with CH3CO2-

If the species is a better leaving group, it reacts faster with the nucleophile.

Here, both the substrates are different. Bromoethane is a primary alkane,bromocyclohexane is a secondary alkane andSN2reaction is shown by primary alkane showing a single-step reaction.

Bromoethane is a better leaving group thanbromocyclohexane

Bromoethaneshows fast reaction thanbromocyclohexane

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 91Ó°ÊÓ!

One App. One Place for Learning.

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

Get started for free

Study anywhere. Anytime. Across all devices.