Hydrocarbons Flashcards

1
Q

Hydrocarbons

A

Made of hydrogen and carbon only, Balancing reactions: carbon —> hydrogen —> oxygen

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2
Q

Types of hydrocarbons

A

Types: Aliphatic (straight chain), Alicyclic (ring)- not in course, Aromatic (benzene, C6H6)

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3
Q

Types of aliphatics

A

Alkane- Saturated (single bonds), CnH2n+2, Alkene- unsaturated, CnH2n, Alkyne- unsaturated, triple bond (not in course)

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4
Q

Alkanes properties

A

Structural isomers (same number of carbons)
Physical properties: Low melting and boiling point- as chain length increases (larger surface area), melting/boiling point increases due to stronger dispersion forces, Low density- as chain length increases, density increases, Insoluble in water as they are non-polar and water is polar
Chemical properties: Undergo combustion reactions- complete produces CO2 and lots of energy, incomplete produces CO, Substitution reactions- swap hydrogen for halogen, use a catalyst of UV light

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5
Q

Alkenes properties

A

Structural and geometric isomers,
Physical properties (same as all covalent molecules are the same): Low melting and boiling point- as chain length increases (larger surface area), melting/boiling point increases due to stronger dispersion forces, Low density- as chain length increases, density increases, Insoluble in water as they are non-polar and water is polar
Chemical properties:
Undergo combustion reactions, Addition reactions- breaks double bond

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6
Q

Aromantic (benzene)

A

Each carbon is covalently bonded to 2 carbons and 1 hydrogen, 4th electron is delocalised allowing it to move freely between orbitals

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7
Q

Aromantic (benzene) properties

A

Physical properties: Can’t conduction electricity as it is a discrete molecule, Low melting and boiling point however high considering it’s a small molecule because it has a high surface area allowing molecules to get closer together, increasing dispersion forces, Higher density then expected due to molecules being able to get close, Insoluble in water
Chemical properties: Combustion reactions, Substitution reactions

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8
Q

Alcohol group

A

Hydroxyl group (-OH), suffix- ol

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9
Q

Aldehydes group

A

Carbonyl group (-CHO with carbon-oxygen double bond), suffix- al, always on carbon 1

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10
Q

Ketone group

A

Carbonyl group (-CO-), suffix- one

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11
Q

Carboxylic acid group

A

Carboxyl group (-COOH), suffix- oic acid, always on carbon 2

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12
Q

Esters group

A

Alkyl group attached to oxygen, suffix- oate, always on carbon 1

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