Chapter 1 - Nomenclature Flashcards

1
Q

What is the first step to naming an organic molecule?

A

Identify the parent chain using length and functional groups.

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2
Q

What is the second step to naming an organic molecule?

A

Number the chain.

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3
Q

What is the third step to naming an organic molecule?

A

Name the substituents.

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4
Q

Carbon chain substituents suffix

A

replace -ane with -yl

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5
Q

What are the qualifiers for carbon chain substituents?

A

n- (normal), t-(t shaped), iso- (split chain, open mouth), sec- (results in a secondary alcohol).

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6
Q

What is the fourth step to naming an organic molecule?

A

Assign a number to each substituent.

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7
Q

What do you ignore when alphabetizing?

A

prefixes, n-, and tert-

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8
Q

What do you include when alphabetizing?

A

iso-, neo-, and cyclo-

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9
Q

What is the fifth step of naming an organic molecule?

A

Alphabetize what you have and put it together.

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10
Q

What are the fundamental characteristics of alkanes?

A

Simple hydrocarbon molecules with formula CnH(2n+2)

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11
Q

How do you name halogen substituents?

A

replace -ide with o-. ex. fluoro-, chloro-, bromo-, iodo-

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12
Q

What are the fundamental characteristics of alkenes and alkynes?

A

Hydrocarbons with double and triple bond respectively. They are named -ene and -yne.

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13
Q

What are the fundamental characteristics of alcohols?

A

Carbon bound to an -OH group. Parent chains are named -ol, substituents are named hydroxy-

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14
Q

What are geminal diols (hydrates) and vicinal diols?

A

A geminal diol (hydrate) is two alcohols on the same carbon. A vicinal diol is two adjacent alcohols (vicinity).

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15
Q

What are the fundamental characteristics of aldehydes?

A

Carbonyl group on the end of a chain. These are named by replacing the -e of the alkane with -al. Substituents are named oxo-

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16
Q

What do you call the common name aldehydes?

A

Formaldehyde (methanal), acetaldehyde (ethanal), propionaldehyde (propanal).

17
Q

What are the fundamental characteristics of ketones?

A

Carbonyl group anywhere but the end of a chain. Replace -ane with -one. Substituent keto groups are named oxo- or keto-.

18
Q

What do you call the common name ketone?

A

Acetone (propanone) or alphabetical alkyl groups followed by ketone.

19
Q

How does one use the greek naming conventions?

A

alpha indicates adjacent carbon. beta is the next carbon, followed by gamma, and finally delta.

20
Q

What are the fundamental characteristics of Carboxylic Acids?

A

Both a carbonyl and a hydroxyl group on a terminal carbon. Replace -e in alkane with -oic acid.

21
Q

What are the common names of carboxylic acids?

A

Formic acid (methanoic acid), acetic acid (ethaoic acid) and propionic acid (propanoic acid).

22
Q

What are the Carboxylic acid derivatives?

A

Esters, Amids, and anhydrides.

23
Q

What are the fundamental characteristics of Esters?

A

A carbonyl and a alkoxy (-OR) group. Name by describing the alkyl name of the esterifying group and then the parent acid with -oate instead of -oic acid.

24
Q

What are the fundamental characteristics of Amides?

A

A carbonyl and an amino group. Named by describing alkyl name of amino group and parent acid replaced with -amide.

25
Q

How do you name alkyl groups that are attached to a Nitrogen?

A

N-alkyl name.