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

Question: What alkane is needed to make each alkyl halide by radical halogenation?

Short Answer

Expert verified

Answer

Step by step solution

01

Radical halogenation

The halogenation reaction involving the replacement of a highly reactive hydrogen atom of alkanes or alkyl substituted aromatics by any of the halide ions initiated by either heat or UV light is known as the radical halogenation reaction.

02

Identifying alkanes

The given alkyl halides are produced by the free-radical halogenation of the following compounds:


a) Replacing the bromide ion by hydrogen atom would give the corresponding alkane.


2-methyl butane

b) The halide ion is replaced by a hydrogen atom to form the corresponding hydrocarbon

Propyl cyclohexane

c) The chloride ion is replaced by the hydrogen atom to form the corresponding alkane.

2,2-Dimethyl propane

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

Most popular questions from this chapter

Question: Identify the structure of a minor product formed from the radical chlorination of propane, which has molecular formula C3H6Cl2 and exhibits the given 1H NMR spectrum.

Question: Draw all resonance structures of the radical that results from abstraction of a hydrogen atom from the antioxidant BHA (butylated hydroxy anisole).

Question: With reference to the indicated C-H bonds in 2-methylbutane.

a. Rank the C-H bonds in order of increasing bond length.

b. Draw the radical resulting from cleavage of each C-H bond and classify it as 10,20, or 30

c.Rank the order of radicals in order of increasing stability.

Rank the C-H bonds in order of increasing ease of H abstractions in a radical halogenation reaction.

Question: (a)Hard contact lenses, which first became popular in the 1960s, were made by polymerizing methyl methacrylate [CH2=C(CH3)CO2CH3] to form poly(methyl methacrylate) (PMMA). Draw the structure of PMMA. (b) More comfortable softer contact lenses introduced in the 1970swere made by polymerizing hydroxyethyl methacrylate [CH2=C(CH3)CO2CH2CH2OH] to form

poly(hydroxyethyl methacrylate) (poly-HEMA). Draw the structure of poly-HEMA. Since neither polymer allows oxygen from the air to pass through to the retina, newer contact lenses that are both comfortable and oxygen-permeable have now been developed.

Question: Show all steps and reagents needed to convert cyclohexane into each compound: (a) the two enantiomers of trans-1,2-dibromocyclohexane; and (b) 1,2-epoxycyclohexane.

See all solutions

Recommended explanations on Chemistry Textbooks

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