Paper 2 Flashcards

(16 cards)

1
Q

Homologous series

A

A series of organic compounds having the same functional group but with each successive member differing by CH2.

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2
Q

Functional group

A

A group of atoms responsible for the characteristic reactions of a compound.

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3
Q

Aliphatic

A

A compound containing carbon and hydrogen atoms joined together in straight chains, branched chains or non-aromatic rings.

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4
Q

Alicyclic

A

An aliphatic compound arranged in non-aromatic rings with or without side chains.

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5
Q

Aromatic

A

A compound containing a benzene ring.

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6
Q

Structural isomers

A

Compounds with the same molecular formula but different structural formulae.

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7
Q

Homolytic fission

A

Each bonding atom receiving one electron from the bonded pair, forming two radicals.

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8
Q

Heterolytic fission

A

One bonding atom receiving both electrons from the bonded pair.

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9
Q

Radical

A

A species with an unpaired electron.

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10
Q

Stereoisomers

A

Compounds with the same structural formula but with a different arrangement in space.

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11
Q

E/Z isomerism

A

An example of stereoisomerism in terms of restricted rotation about a double bond and the requirement for two different groups to be attached to each carbon atom of the C=C.

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12
Q

cis-trans isomerism

A

A special case of E/Z isomerism in which two of the substituent groups attached to each carbon atom of the C=C group are the same.

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13
Q

Electrophile

A

An electron pair acceptor.

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14
Q

Nucleophile

A

An electron pair donor.

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15
Q

What shape does the bonds around each carbon atom in an alkane form?

A

Each carbon atom has 4 bonding pairs of electrons. They all repel each other equally. So the molecule forms a tetrahedral shape around each carbon and each bond angle is 109.5 degrees.

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16
Q

What does the boiling point of an alkane depend on?

A

Between the molecules there are induced dipole-dipole interactions (London forces) which hold them all together. The longer the carbon chain, the stronger the London forces. This is because there’s more surface contact and more electrons to interact. As the molecules get longer it takes more energy to overcome the London forces and the boiling point rises. A branched-chain alkane has a lower boiling point that its straight-chain isomer. Branched-chain alkanes can’t pack closely together and they have smaller molecular surface areas - so the London forces are reduced.