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 15: Q 15-15-18 E-f (page 477)

Give IUPAC names for the following compounds

f)

Short Answer

Expert verified

f)

4-chloroaniline

Step by step solution

01

What is IUPAC?

For chemical compounds, the rules of naming are set by IUPAC (the international union of pure and applied chemistry)

02

IUPAC name of a compound

In the provided compound f, the name of the parent hydrocarbon is aniline. Numbering the ring in such a way that the functional group and substituent get the lowest possible number.

03

Position of functional group in compound

The chlorine group is at the fourth carbon para to the amine group. Thus, the IUPAC name of the compound is 4-chloroaniline that is represented as:

4-chloroaniline

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

All-cis cyclodecapentaene is a stable molecule that shows a single absorption in its NMR spectrum at 5.67δ. Tell whether it is aromatic, and explain its NMR spectrum.

Azulene, a beautiful blue hydrocarbon, is an isomer of naphthalene. Is azulene aromatic? Draw a second resonance form of azulene in addition to that shown.

Draw and name all possible isomers of the following:

  1. Dinitrobenzene
  2. Bromo dimethyl benzene
  3. Trinitrophenol

To be aromatic, a molecule must have 4n+2 p electrons and must have a planar, monocyclic system of conjugation. Cyclodecapentaene fulfills one of these criteria but not the other and has resisted all attempts at synthesis. Explain.

Draw structures corresponding to the following names:

(a) 3-Methyl-1,2-benzenediamine

(b) 1,3,5-Benzenetriol

(c) 3-Methyl-2-phenylhexane

(d) o-Aminobenzoic acid

(e) m-Bromophenol

(f) 2,4,6-Trinitrophenol (picric acid)
See all solutions

Recommended explanations on Chemistry Textbooks

Physical Chemistry

Read Explanation

Nuclear Chemistry

Read Explanation

Inorganic Chemistry

Read Explanation

Ionic and Molecular Compounds

Read Explanation

Chemistry Branches

Read Explanation

The Earths Atmosphere

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