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: Give the IUPAC name for each of the five constitutional isomers of molecular formula C6H14 in Problem 4.3.

Short Answer

Expert verified

Answer

  • Hexane
  • 2-methylpentane
  • 3-methylpentane
  • 2,2-dimethylbutane
  • 2,3-dimethylbutane

Step by step solution

01

IUPAC naming 

Rules for IUPAC naming:

  • The longest chain of carbon atoms is selected.
  • The counting is started from the carbon with maximum substitution.
  • The functional groups are given the highest priority.
02

Isomers of  C6H14

The isomers of the given compound are represented below:

Isomers of C6H14

03

Explanation

  • The IUPAC name of the first isomer is hexane as it has a linear chain.
  • The IUPAC name of the second isomer is 2-methylpentane as it has a chain of five carbons with a methyl group at the second position.
  • The IUPAC name of the third isomer is 3-methylpentane as it has a chain of five carbons with a methyl group at the third position.
  • The IUPAC name of the fourth isomer is 2,2-dimethylbutane as it has a chain of four carbons with two methyl groups at the second position.
  • The IUPAC name of the fifth isomer is 2,3-dimethylbutane as it has a chain of four carbons and two methyl groups at the second and third positions.

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: Rank the following alkanes in order of increasing boiling point.

Question: For each compound drawn below:

a. Draw representations for the cis and trans isomers using a hexagon for the six membered ring, and wedges and dashed wedges for substituents.

b. Draw the two possible chair conformations for the cis isomer. Which conformation, if either, is more stable?

c. Draw the two possible chair conformations for the trans isomer. Which conformation, if either, is more stable?

d. Which isomer, cis or trans, is more stable and why?

Question: Convert each of the following structures into its more stable chair form. One structure represents menthol and one represents isomenthol. Menthol, the more stable isomer, is used in lip balms and mouthwash. Which structure corresponds to menthol?

Question: Consider the tricyclic structure B.

(a) Label each substituent on the rings as axial or equatorial.

(b) Draw B using chair conformations for each six-membered ring.

(c) Label the atoms on the ring fusions (the carbons that join each set of two rings together) as cis or trans to each other.

B

Question: Draw a chair conformation of cyclohexane with one CH3CH2 group and one role="math" localid="1648542173942" CH3 group that fits each description.

  1. a 1,1-disubstituted cyclohexane with an axial role="math" localid="1648542231267" CH3CH2 group
  2. a cis-1,2-disubstituted cyclohexane with an axial role="math" localid="1648542270917" CH3 group
  3. a trans-1,3-disubstituted cyclohexane with an equatorial CH3 group
  4. a trans-1,4-disubstituted cyclohexane with an equatorialCH3CH2 group
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