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

The proton NMR spectrum of a compound with formula C6H5NCl2is shown. The normal carbon-13 and DEPT experimental results are tabulated. The infrared spectrum shows peaks at 3432 and 3313 cm-1and a series of medium-sized peaks between 1618 and 1466 cm-1. Draw the structure of this compound.

Azo dyes are the major source of artificial color in textiles and food. Part of the reason for their intense coloring is the conjugation from an electron-donating group through the diazo bridge (-N=N-)to an electron-withdrawing group on the other side. For the azo dyes below, draw a resonance form that shows how the electron-donating group is related to the electron-withdrawing group on the other side of the diazo bridge. Used curved arrows to show how the electrons are reorganized.

a.

Methyl orange

b.

C.I. Acid Red 74

Which would you expect to be most stable, Cyclononatetraenyl radical, cation, or anion?

The compound below is the product initially formed in a Claisen rearrangement (Section 18-4). This product is not isolated but tautomerizes to its enol form. Give the structure of the enol and provide an explanation as to why the enol tautomer is favored.

7 Propose structures for aromatic compounds that have the following 1HNMR spectra:

(a) C8H9BrIR=820 cm-1

b) C9H12IR:750 cm-1

c) C11H16IR:820 cm-1
See all solutions

Recommended explanations on Chemistry Textbooks

Ionic and Molecular Compounds

Read Explanation

Chemistry Branches

Read Explanation

Making Measurements

Read Explanation

Nuclear Chemistry

Read Explanation

The Earths Atmosphere

Read Explanation

Inorganic 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