Nomenclature Rules Flashcards

1
Q

What is the first step in determining IUPAC?

A

Find the longest carbon chain with THE MOST SUBSTITUENTS and determine the parent name

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2
Q

What is the second step in determining IUPAC?

A

Name all of the substituents on the main chain using -yl as the ending of the base name; use prefixes for multiple types of one substituent

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3
Q

What is the third step in determining IUPAC?

A

Number the carbons on the parent chain TO OBTAIN THE LOWEST OVERALL NUMBERS of each substituent

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4
Q

What is the fourth step in determining IUPAC?

A

Write the name of the molecule in alphabetical order with the parent name at the end

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5
Q

What are formatting rules when writing the name of a molecule?

A

Dashes go between numbers, letters, and parentheses; commas go between numbers; complex substituents go in parentheses; no spaces in the name

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6
Q

When a molecule has multiple of the same substituent, how are the numbers written when determining the name?

A

They are written in ascending order (ex. 2, 5, 7-trimethylnonane)

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7
Q

What do you do if the substituents are evenly dispersed over the parent chain number wise?

A

Give the lowest number according to alphabetical order

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8
Q

What happens if di, tri, etc. are part of substituent names?

A

They do NOT count alphabetically

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9
Q

What changes when naming a molecule with branched common names like sec- and tert-?

A

They do not count alphabetically or require parentheses; however, iso- and neo- do count alphabetically

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10
Q

What are things to know concerning functional group specifics?

A

The highest priority functional group must be in the base chain and have the lowest number when possible; stereochemical information always goes in front of the name in parentheses using numbers to specify the stereocenter/branch point when necessary

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11
Q

How do we name Haloalkanes?

A

Treat halogens as substituents (no priority) with an -o ending (fluoro-, chloro-, bromo-, and iodo-)

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