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Chapter 15: Q 15-15-18 E-d (page 477)

Give IUPAC names for the following compounds

d)

Short Answer

Expert verified

d)

1-bromo-2-propylbenzene

Step by step solution

01

What is IUPAC?

According to IUPAC (the international union of pure and applied chemistry), an organic compound in chemistry should be named after the union's standards.

02

IUPAC name of the compound

In the provided compound d, the name of the parent hydrocarbon is benzene. I am numbering the ring so that the functional group and substituent get the lowest possible number.

03

Position of functional group in compound

The bromine group is at the first carbon, and the ethyl group is at the second carbon atom. Thus, the IUPAC name of the compound d is 1-Bromo-2-propylbenzene represented as:

bromo-2-propylbenzene

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Most popular questions from this chapter

Cycloheptatrienone is stable, but cyclopentadienone is so reactive that it can’t be isolated. Explain, taking the polarity of the carbonyl group into account.

Cycloheptatrienone Cyclopentadienone

In 1932, A. A. Levine and A. G. Cole studied the ozonolysis of o-xylene and isolated three products: glyoxal, 2,3-butanedione, and pyruvaldehyde:

In what ratio would you expect the three products to be formed if o-xylene is a resonance hybrid of two structures? The actual ratio found was 3 parts glyoxal, 1 part 2,3-butanedione, and 2 parts pyruvaldehyde. What conclusions can you draw about the structure of o-xylene?

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

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.

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