Logout Open In App
Open In App
Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Chapter 8: Q70aE. (page 262)

We’ll see in the next chapter that alkynes undergo many of the same reactions that alkenes do. What product might you expect from each of the following reactions?

Short Answer

Expert verified

The reaction is an example of electrophilic addition. A brominium ion is formed when alkyne undergoes elecrophilic addition reaction.

Step by step solution

01

Introduction

The reaction is an example of electrophilic addition. A brominium ion is formed when alkyne undergoes elecrophilic addition reaction.

02

Chemical reaction involved

03

Reaction of alkyne with halide

When alkyne reacts with halide, they undergo an additional reaction to form halogen substituted alkene. Alkyne followsMarkovnikovregiochemistry in which two added halogen atoms are always in a trans relationship with each other.

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.

Start your free trial

Over 30 million students worldwide already upgrade their learning with Vaia!

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

Compound A has the formula C10H16. On catalytic hydrogenation over palladium, it reacts with only 1 molar equivalent of H2. Compound A also reacts with ozone, followed by zinc treatment, to yield a symmetrical diketone, B(C10H16O2).

Write the reactions.

Simmons–Smith reaction of cyclohexene with diiodomethane gives asingle cyclopropane product, but the analogous reaction of cyclohexene with 1,1-diiodoethane gives (in low yield) a mixture of two isomeric methylcyclopropane products. What are the two products, and how do they differ?

Question: In planning the synthesis of one compound from another, it’s just as important to know what not to do as to know what to do. The following reactions all have serious drawbacks to them. Explain the potential problems of each.

We’ll see in the next chapter that alkynes undergo many of the same reactions that alkenes do. What product might you expect from each of the following reactions?

Question:Which reaction would you expect to be faster, the addition of HBr to cyclohexene or 1-methylcyclohexene? Explain.
See all solutions

Recommended explanations on Chemistry Textbooks

The Earths Atmosphere

Read Explanation

Inorganic Chemistry

Read Explanation

Nuclear Chemistry

Read Explanation

Chemistry Branches

Read Explanation

Ionic and Molecular Compounds

Read Explanation

Organic 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.

Sign-up for free