S3.2.2 Functional groups

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14 Terms

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Alkyl

Saturated hydrocarbons with C–C single bonds.

General formula: CnH2n+2.

Reactions: Combustion, Free radical substitution.

<p>Saturated hydrocarbons with C–C single bonds. </p><p>General formula: C<sub>n</sub>H<sub>2n+2. </sub></p><p>Reactions: Combustion, Free radical substitution.</p>
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Alkenyl

Unsaturated hydrocarbons with C=C double bonds.

General formula: CnH2n.

Reactions: Combustion, Electrophilic addition, Reduction to alkanes.

<p>Unsaturated hydrocarbons with C=C double bonds. </p><p>General formula: C<sub>n</sub>H<sub>2n</sub>. </p><p>Reactions: Combustion, Electrophilic addition, Reduction to alkanes.</p>
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Alkynyl

Unsaturated hydrocarbons with C≡C triple bonds.

General formula: CnH2n-2.

Reactions: Combustion, Electrophilic addition.

<p>Unsaturated hydrocarbons with C≡C triple bonds. </p><p>General formula: C<sub>n</sub>H<sub>2n-2</sub>. </p><p>Reactions: Combustion, Electrophilic addition.</p>
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Aldehyde

Carbonyl group (C=O) bonded to H.

General formula: CnH2nO.

Reactions: Oxidation to acids, Reduction to primary alcohols (HL only).

<p>Carbonyl group (C=O) bonded to H.</p><p>General formula: C<sub>n</sub>H<sub>2n</sub>O.</p><p>Reactions: Oxidation to acids, Reduction to primary alcohols (HL only).</p>
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Ketones

Carbonyl group (C=O) bonded to two R groups.

General formula: CnH2nO.

Reactions: Reduction to secondary alcohols (HL only).

<p>Carbonyl group (C=O) bonded to two R groups.</p><p>General formula: C<sub>n</sub>H<sub>2n</sub>O.</p><p>Reactions: Reduction to secondary alcohols (HL only).</p>
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Esters

COO group between two alkyl groups.

General formula: CnH2nO2.

Formed by alcohol + acid, undergo hydrolysis.

<p>COO group between two alkyl groups.</p><p>General formula: C<sub>n</sub>H<sub>2n</sub>O<sub>2</sub>.</p><p>Formed by alcohol + acid, undergo hydrolysis.</p>
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Ethers

Oxygen atom bonded to two alkyl groups.

General formula: CnH2n+2O

No reactions in IB syllabus.

<p>Oxygen atom bonded to two alkyl groups.</p><p>General formula: C<sub>n</sub>H<sub>2n+2</sub>O</p><p>No reactions in IB syllabus.</p>
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Hydroxyl

Contain -OH (hydroxy) group.

General formula: CnH2n+2O.

Reactions: Combustion, Oxidation, Esterification.

<p>Contain -OH (hydroxy) group. </p><p>General formula: C<sub>n</sub>H<sub>2n+2</sub>O. </p><p>Reactions: Combustion, Oxidation, Esterification.</p>
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Carboxyl

Contain COOH (carboxy) group.

General formula: CnH2nO2.

Reactions: With alcohols to form esters, Reduction (HL only).

<p>Contain COOH (carboxy) group.</p><p>General formula: C<sub>n</sub>H<sub>2n</sub>O<sub>2</sub>.</p><p>Reactions: With alcohols to form esters, Reduction (HL only).</p>
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Nitriles

Contain C≡N triple bond.

General formula: CnH2n+1N.

Reactions not covered in IB.

<p>Contain C≡N triple bond. </p><p>General formula: C<sub>n</sub>H<sub>2n+1</sub>N. </p><p>Reactions not covered in IB.</p>
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Amines

Contain -NH2 or N bonded to alkyl groups.

General formula: CnH2n+3N.

Act as Brønsted and Lewis bases.

<p>Contain -NH2 or N bonded to alkyl groups.</p><p>General formula: C<sub>n</sub>H<sub>2n+3</sub>N.</p><p>Act as Brønsted and Lewis bases.</p>
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Amides

Contain CONH2 group.

General formula: CnH2n+1NO.

Reactions not covered in IB.

<p>Contain CONH2 group. </p><p>General formula: C<sub>n</sub>H<sub>2n+1</sub>NO. </p><p>Reactions not covered in IB.</p>
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Phenyl

Aromatic compounds with phenyl group.

Benzene molecule minus a hydrogen atom

Reactions (HL): Reduction of nitrobenzene.

<p>Aromatic compounds with phenyl group.</p><p>Benzene molecule minus a hydrogen atom</p><p>Reactions (HL): Reduction of nitrobenzene.</p>
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Halogenoalkanes

Alkane with halogen (F, Cl, Br, I).

General formula: CnH2n+1X.

Reactions: Nucleophilic substitution.

<p>Alkane with halogen (F, Cl, Br, I). </p><p>General formula: C<sub>n</sub>H<sub>2n+1</sub>X. </p><p>Reactions: Nucleophilic substitution.</p>