Organic Chemistry Ch 1. Nomenclature Flashcards

1
Q

IUPAC naming steps

A

1) Find the longest carbon chain in the compound that contains the highest priority functional group, this is called the parents chain
2) Number the chain in such a way that the highest priory functional group group receives the lowest possible number, this group will determine the suffix of the molecules
3) Name the substituents with a prefix, multiple substituents of a single type receive another prefix denoting how many are present (di, tri, tetra and so on)
4) Assign a number to each of the substituents depending on the carbon to which it is bonded
5) Complete the name by alphabetizing the substituents and separating number from each other by commas and from works by hyphens

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2
Q

Alkanes

A

Hydrocarbons without any double or triple bonds, have the general formula C(n)H(2n+2), named according to the number of carbons present followed by suffix -ane

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3
Q

Alkenes

A

Contain a double bond, named by substituting -ene for the suffix and numbering the double bond by its lower-numbered carbon

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4
Q

Alkyne

A

Contains a triple bond, named by substituting -yne for the suffix and numbering the double bond by its lower-numbered carbon

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5
Q

Alcohol

A

Contain a hydroxyl group (OH) group, which substitutes for one or more of the hydrogens in the hydrocarbon chain, named by substituting the suffix -ol or by using the prefix hydroxy- if a higher priority group is present, have higher priority than double or triple bonds

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6
Q

Diols

A

Contain two hydroxyl groups

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7
Q

Germinal

A

Diol that has the two hydroxyl groups on the same carbon

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8
Q

Vicinal

A

Diol that has the two hydroxyl groups but on adjacent carbons

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9
Q

Carbonyl group

A

A carbon doubled bonded to an oxygen

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10
Q

Aldehydes

A

Have a carbonyl group on a terminal carbon that is also attached to a hydrogen atom, named with the suffix -al or by using the prefix oxo- if a higher priority group is present

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11
Q

Ketons

A

Have a carbonyl group on a non terminal carbon, named with the suffix -one and share the prefix oxo- if a higher priority group is present, can also be indicated by the prefix keto-

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12
Q

Alpha carbon

A

Carbon adjacent to the carbonyl carbon

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13
Q

Carboxylic acids

A

The highest priority functional group because they contain three bonds to oxygen: One from a hydroxyl group and two from a carbonyl group, always terminal, named with the suffix -oic acid, rarely named with prefix

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14
Q

Carboxylic acid derivatives

A

May occur within a molecule, includes esters, amides, and anhydrides

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15
Q

Esters

A

Carboxylic acid derivative where -OH is replaced with -OR, an alkoxy group, use the suffix -oate and the prefix alkoxycarbonyl-

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16
Q

Amides

A

Replace the hydroxyl group of the carboxylic acid with an amino group that may or may not be substituted, use the suffix -amide or the prefix carbamoyl- or amido-, substituents attached to the amide nitrogen are designated with a capital N -

17
Q

Anhydrides

A

Formed from two carboxylic acids by dehydration, they may e symmetric (two of the same acid) or asymmetric (two different acids) or cyclic (intramolecular reaction of a dicarboxylic acid), named using the suffix anhydride in place of acid, if the anhydride is formed from more than one carboxylic acid, both are named in alphabetical order in the name before the word anhydride

18
Q

Functional group priority

A

Carboxylic acids>anhydride>ester>amide>aldehyde>ketone>alcohol>aklene or alkyne> alkane