Chemistry! !write the iupac name of the compound represented by the structural formula shown.

Answers:

1. 3-ethyl-3-methylheptane; 2. 2,2,3,3-tetramethylpentane; 3. hexa-2,4-diene.

Explanation:

Structure 1

Identify and name the longest continuous chain of carbon atoms (the main chain has 7 C; ∴ base name = heptane). Identify and name all the substituents [a 1C substituent (methyl) and a 2C substituent (methyl). Number the main chain from the end closest to a substituent. Identify the substituents by the number of the C atom on the main chain. Use hyphens between letters and numbers (3-methyl, 3-ethyl). Put the names of the substituents in alphabetical order in front of the base name with no spaces (3-ethyl-3-methylheptane)

Structure 2

5C. Base name = pentane Four methyl groups. Number from the left-hand end. If there is more than one substituent of the same type, identify each substituent by its locating number and use a multiplying prefix to show the number of each substituent. Use commas between numbers (2,2,3,3-tetramethyl). The name is 2,2,3,3-tetramethylpentane.

Structure 3

Identify and name the longest continuous chain of carbon atoms that passes through as many double bonds as possible. Drop the -ne ending of the alkane to get the root name hexa-. (No substituents). Number the main chain from the end closest to a double bond. If there is more than one double bond use a multiplying prefix to indicate the number of double bonds (two double bonds = diene) and use the smaller of the two numbers of the C=C atoms as the double bond locators (2,4-diene) Put the functional group name at the end of the root name (hexa-2,4-diene).

Note: The name 2,4-hexadiene is acceptable, but the Preferred IUPAC Name puts the locating numbers as close as possible in front of the groups they locate.