Give the IUPAC Name

a. 3,4,5-methyl-4-propyloctane

b. 4-propyl-trimethyloctane

c. 4,5,6-trimethylethyoctane

d. 3,4,5-trimethyl-4-propyloctane e. 4,5-dimethyl-4-methylpropyloctane

H3C CH2

CH

CH3

CH

CH3

CH2

CH2

CH3

CH

CH3

CH2

CH2

CH3

Give the IUPAC Name

a. 4-t-butylheptane

b. 4-isobutylheptanec. 4-(1,1-dimethylethyl)heptane

d. 4-(1-methylpropyl)heptanee. a. and c.

Give the IUPAC Name

a. 5-ethyl-4-iodo-2-methyloctaneb. 5-ethyl-4-iodo-2,2-dimethyloctanec. 1,1-dimethyl-3-iodo-4-propyloctaned. 3-iodo-4-ethyl-1,1,1-trimethylheptanee. 4-ethyl-5-iododecane

(H3C)3C CH2

CH

I

CH

CH2CH3

CH2

CH2

CH3

Give the IUPAC Name

a. 2-chloro-5,5-dimethylhexane

b. 1-t-butyl-3-chlorobutane

c. 2-chloro-4-(2-methylpropan-2-yl)butane

d. 2-chloro-4-t-butylbutane

e. 5-chloro-2,2-dimethylhexane

Cl

Alkene and Alkyne Nomenclature Practice

• What is the correct Preferred IUPAC name for the following structure?

a. (Z)-6-methyl-4-propyloct-2-eneb. (Z)-3-methyl-4-(prop-1-en-1-yl)octanec. (Z)-3-methyl-5-(prop-1-en-1-yl)octaned. (E)-6-methyl-4-propyloct-2-enee. (E)-6-methyl-4-(prop-1-en-1-yl)octane

Alkene and Alkyne Nomenclature Practice

What is the correct acceptable IUPAC name for this structure?

a. 1,1-dimethyl-3-butyne

b. 4,4-dimethyl-1-butyne

c. 4-methyl-1-pentyne

d. 2-methyl-4-pentyne

C CCH2

CH

CH3

H3CH

Alkene and Alkyne Nomenclature Practice

• What is the correct Preferred IUPAC name for the following structure?

a. (Z)-6-methyl-4-propyloct-2-eneb. (Z)-3-methyl-4-(prop-1-en-1-yl)octanec. (Z)-3-methyl-5-(prop-1-en-1-yl)octaned. (E)-6-methyl-4-propyloct-2-enee. (E)-6-methyl-4-(prop-1-en-1-yl)octane

Alkene and Alkyne Nomenclature Practice

What is the correct acceptable IUPAC name for this structure?

a. 1,1-dimethyl-3-butyne

b. 4,4-dimethyl-1-butyne

c. 4-methyl-1-pentyne

d. 2-methyl-4-pentyne

C CCH2

CH

CH3

H3CH

Nomenclature of Alcohols(IUPAC preferred)

a. 1-chloro-3-hydroxycyclopentaneb. 1-chlorocylopentan-3-olc. 3-chlorocyclopentan-1-old. 3-chloro-1-hydroxycyclpentanee. 3-chlorocyclpentyl alcohol

Cl

OH

Nomenclature of Alcohols(IUPAC acceptable)

a. 4-chloro-3,3,5-trimethyl-7-octanol

b. 5-chloro-6-ethyl-4,6-dimethyl-2-heptanol

c. 5-chloro-4,6,6-trimethyl-2-octanol

d. 3-chloro-2-ethyl-2,4-dimethyl-6-heptanol

e. 3-chloro-2-ethyl-2,4-methylheptanol

OH

Cl

• What is the IUPAC name for the following compound?

a. (Z)-2-(1-hydroxy-2,2-dimethyl)-2-hexeneb. (Z)-2,2,4-trimethyl-4-octen-3- ol c. (Z)-1-t-butyl-2-methyl-2-hexen-1-old. (E)-2,2,4-trimethyl-4-octen-3- ol e. (E)-1-t-butyl-2-methyl-2-hexen-1-ol

HO

Amine Nomenclature

What is an appropriate name for the following compound?

a. (Z)-3-amino-4-methyl-4-octeneb. (E)-2-(1-aminopropyl)-2-hexenec. (Z)-2-(1-aminopropyl)-2-hexened. (Z)-6-amino-5-methyl-4-octenee. (E)-3-amino-4-methyl-4-octene

H2N

Aromatic Nomenclature Practice

• What is the an appropriate preferred IUPAC name for the following compound?

a. o-bromomethylbenzeneb. 3-bromomethylbenzenec. p-bromomethylbenzened. 2-bromotoluenee. 3-bromotoluene

CH3

Br

Aromatic Nomenclature Practice

• What is the preferred IUPAC name for the following compound?

a. 1-chloro-4-ethyl-3-(propan-2-yl)benzene

b. 1-chloro-5-ethyl-4-(propan-2-yl)benzene

c. 4-chloro-1-ethyl-2-(propan-2-yl)benzene

d. 1-chloro-4-ethyl-5-(propan-2-yl)benzene

e. 1-ethyl-2-(propan-2-yl)-4-chlorobenzene

CH

Cl

H3C CH3

H2C

H3C

Aromatic Nomenclature Practice

• Which of the following structures is aniline?

OCH3 OH C

O H

NH2 C

O NH2

a. b. c. d. e.

IUPAC Nomenclature For Aldehydes and Ketones

a. 2-chloro-1-methylcyclohexanoneb. 4-chloro-5-methylcyclohexanone c. 3,4-chloromethylcyclohexanone d. 1-chloro-2-methylcyclohexanone e. 4-chloro-3-methylcyclohexanone

O

CH3

Cl

IUPAC Nomenclature For Aldehydes and Ketones

a. (E)-pent-2-ene-1,5-dioneb. (E)-hex-2-ene-2,5-dione c. (E)-4-oxopent-2-enal d. (E)-2-oxopent-3-enal e. (E)-4-oxypent-2-enal

O

H

O

IUPAC Nomenclature For Aldehydes and Ketones

• What is the preferred name for salicylaldehyde?

a. 2-hydroxybenzaldehydeb. o-hydroxybenzaldehydec. 2-hydroxybenzenecarbaldehyded. o-hydroxybenzenecarbaldehyde

C

H

O

OH