Functional Groups Flashcards

(13 cards)

1
Q

Alkane

A

C–C single bonds only. Suffix: –ane.
e.g. CH₄ (methane).

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2
Q

Alkene

A

Contains C=C double bond. Suffix: –ene.
e.g. CH₂=CH₂ (ethene).

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3
Q

Alkyne

A

Contains C≡C triple bond. Suffix: –yne.
e.g. CH≡CH (ethyne).

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4
Q

Haloalkane/halogeno

A

Contains C–X (X = F, Cl, Br, I).
e.g. CH₃Cl (chloromethane).

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5
Q

Hydroxyl (Alcohol)

A

Contains –OH group. Suffix: –ol.
e.g. CH₃CH₂OH (ethanol).

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6
Q

Alkoxy (Ether)

A

Contains C–O–C linkage. Name: alkoxy- (e.g. methoxyethane).
Shorter chain always the oxy

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7
Q

Carbonyl (Aldehyde)

A

–CHO (C=O at end of chain). Suffix: –al.
e.g. CH₃CHO (ethanal).

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8
Q

Carbonyl (Ketone)

A

C=O within chain (not terminal). Suffix: –one.
e.g. CH₃COCH₃ (propanone).

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9
Q

Carboxyl (Carboxylic acid)

A

–COOH (C=O and –OH on same C). Suffix: –oic acid.
e.g. CH₃COOH (ethanoic acid).

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10
Q

Ester

A

–COO– (derived from acid + alcohol). Suffix: –oate.
e.g. CH₃COOCH₃ (methyl ethanoate).
Side with carbon double bond to oxygen is the oate.

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11
Q

Amide/Amido

A

–CONH₂ (carbonyl + amine). Suffix: –amide.
e.g. CH₃CONH₂ (ethanamide).

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12
Q

Amino (Amine)

A

–NH₂ (basic group). Prefix: amino– or suffix: –amine.
e.g. CH₃CH₂NH₂ (ethylamine).

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13
Q

Phenyl (Benzene ring)

A

C₆H₅– group. Aromatic ring (π delocalisation).
e.g. C₆H₅CH₃ (methylbenzene).

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