Chapter 2: Nomenclature Flashcards

1
Q

What is a functional group?

A

A small collection of atoms in a molecule that determines its chemical reactivity and properties

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2
Q

What are the four types of functional groups that contain only C and H?

A

Alkane, Alkene, Alkyne, Arene (Aromatic compounds).

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3
Q

What functional groups contain oxygen?

A

Alcohol, Ether, Aldehyde, Ketone, Carboxylic Acid, Ester, Anhydride.

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4
Q

What functional groups contain nitrogen?

A

Amine, Amide, Nitrile, Nitro group.

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5
Q

What functional groups contain halogens?

A

Alkyl halide

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6
Q

What functional groups contain a carbonyl (C=O) group?

A

Aldehyde, Ketone, Carboxylic Acid, Ester, Amide, Acid Halide, Anhydride.

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7
Q

What functional group is present in CH₃CH₂OH?

A

Alcohol (-OH)

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8
Q

What functional group is present in CH₃COCH₃?

A

Ketone (C=O in the middle of a chain).

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9
Q

What functional group is present in HCOOH?

A

Carboxylic Acid (-COOH).

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10
Q

What functional group is present in CH₃CH₂NH₂?

A

Amine (-NH₂).

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11
Q

What functional group is present in CH₃CH₂COOCH₃?

A

Ester (-COO-).

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12
Q

What functional group is absent in benzene?

A

Alkene (though benzene has double bonds, they are delocalized in an aromatic ring).

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13
Q

What are the four parts of an IUPAC name?

A

Prefix, Parent, Locant, Suffix.

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14
Q

What does the “parent” part of a name indicate?

A

The longest continuous carbon chain.

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15
Q

What does the “prefix” part of a name indicate?

A

Substituents (e.g., methyl, ethyl, chloro).

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16
Q

What does the “locant” indicate?

A

The position of the functional group or substituent on the carbon chain.

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17
Q

What does the “suffix” indicate?

A

The main functional group in the molecule.

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18
Q

What is the suffix for an alkane?

A

“-ane” (e.g., methane, ethane).

19
Q

What is the suffix for an alkene?

A

“-ene” (e.g., ethene, propene).

20
Q

What is the suffix for an alkyne?

A

“-yne” (e.g., ethyne, propyne).

21
Q

What is the suffix for a carboxylic acid?

A

“-oic acid” (e.g., ethanoic acid).

22
Q

What is the suffix for an ester?

A

“-oate” (e.g., ethyl ethanoate).

23
Q

What is the parent name for a 7-carbon alkane?

A

Heptane (C₇H₁₆).

24
Q

What is the parent name for a 5-carbon cycloalkane?

A

Cyclopentane (C₅H₁₀).

25
Q

What is the correct name for CH₃CH₂CH₂CH₃?

26
Q

What is the correct name for a four-carbon cyclic alkane?

A

Cyclobutane.

27
Q

How do you number the carbon chain when naming an alkane?

A

Start from the end nearest to the first substituent to give the lowest possible numbers.

28
Q

What is an alkyl group?

A

A group derived from an alkane by removing one hydrogen (e.g., methyl, ethyl).

29
Q

What is the difference between an isopropyl and a sec-butyl group?

A

Isopropyl (-CH(CH₃)₂) is derived from propane, while sec-butyl (-CH(CH₃)CH₂CH₃) is derived from butane.

30
Q

What are the prefixes for halogen substituents?

A

Fluoro (F), Chloro (Cl), Bromo (Br), Iodo (I).

31
Q

What are the prefixes for ether substituents?

A

Methoxy (-OCH₃), Ethoxy (-OCH₂CH₃).

32
Q

How do you prioritize functional groups when naming a compound?

A

The group with the highest priority gets the suffix, and lower-priority groups are written as prefixes.

33
Q

Which functional group has the highest priority in nomenclature?

A

Carboxylic Acid (-COOH).

34
Q

Which functional groups do not need a locant in their names?

A

Carboxylic acids, Aldehydes, Amides, Nitriles.

35
Q

How do you number the parent chain when multiple substituents are present?

A

Number the chain to give the lowest possible numbers to the highest priority functional group.

36
Q

What is the parent name for benzene with a methyl group?

37
Q

What is the prefix for a benzene ring acting as a substituent?

A

Phenyl (C₆H₅-).

38
Q

What is the prefix for a benzyl group (-CH₂C₆H₅)?

A

Benzyl (Bn-).

39
Q

What are the three types of disubstituted benzene orientations?

A

Ortho (1,2-), Meta (1,3-), Para (1,4-).

40
Q

How are esters named?

A

The alkyl group attached to oxygen is named first, followed by the carboxylate name (e.g., ethyl ethanoate).

41
Q

How are amines named?

A

Alkyl groups attached to nitrogen are named first with an “N-“ prefix (e.g., N-methylpropylamine).

42
Q

How are alkynes named?

A

The suffix “-yne” is used, with numbering indicating the triple bond position (e.g., pent-2-yne).

43
Q

How are cycloalkenes named?

A

The double bond position is always given the lowest number possible in the ring (e.g., cyclohex-1-ene).