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

What products would you expect to obtain from reaction of 1-methylcyclohexanol with the following reagents?

(a) HBr (b) NaH (c) H2SO4 (d) Na2Cr2O7

Short Answer

Expert verified

The treatment of an alcohol with HBr leads to the formation of alkyl bromide. The reaction of alcohols with NaH yields alkoxide. The reaction of alcohols with sulphuric acid leads to the formation of alkenes. Tertiary alcohols do not undergo any reaction when reacted with Na2Cr2O7.

Step by step solution

01

Reaction of alcohols with several reagents

The treatment of an alcohol with HBr leads to the formation of alkyl bromide. The reaction of alcohols with NaH yields alkoxide. The reaction of alcohols with sulphuric acid leads to the formation of alkenes. Tertiary alcohols do not undergo any reaction when reacted with Na2Cr2O7.

02

Reaction of 1-methylcyclohexanol with several reagents

(a) 1-methylcyclohexanol reacts with HBr to produce 1-bromo-1-methylcyclopentane. The reaction can be given as:

(b) 1-methylcyclohexanol reacts with NaH to form sodium-1-methylcyclopentanolate. The reaction can be given as:

(c) 1-methylcyclohexanol reacts with to form 1-methylcylochex-1-ene. The reaction can be given as:

(d) 1-methylcyclohexanol does not react with Na2Cr2O7 as tertiary alcohols are not oxidized by Na2Cr2O7.

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 Vaia!

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.

Sign-up for free